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2024-12-31-accounts

Multiple Sclerosis Society 2024 Annual Report and Accounts

Introduction.

Every MS Story. Our Strategy

Over 150,000 people in the UK have multiple sclerosis (MS). But living with MS is never the same for any two people. Symptoms can be experienced in different ways by different people. And, while some of these are visible, some are not. Some people have all the health and social care they need and support from family, friends and employers, but most don’t. Everyone living with MS has a unique story.

We want a world free from the effects of MS. And we have a bold, ambitious strategy to help get us there. At its core are the MS stories of the 150,000 people living with MS and their families, friends and networks. We’ve listened to people’s stories, and our current strategy is focused on responding to what we know is important to the MS community.

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Foreword

Message from the Chair, Sir Paul Curran

I’m proud of our achievements in what has been another challenging year for people living with MS. In 2024 we released the latest prevalence data for MS, and while over 150,000 people in the country were living with the condition, we estimated that the lives of around six million friends, family and colleagues were also affected. This well illustrates the scale of the task ahead of us. It was also a year when we brought our community together to make sure MS was a priority as the new Government took office. We shared the insight and experience of our community with the Government to help shape their legislative programme. From improvements to sick pay and support for disabled people in work, to the NHS 10-year Health Plan and the newly established UK Neuro Forum, there were opportunities for us to make sure the voices of people living with MS were heard in the corridors of power.

Across the nations, we continued to deliver vital services and support, including our Living Well programme of online support sessions, information events and digital support tools. We also continued to answer calls on our MS Helpline and offered practical advice on benefits and welfare, while our MS Nurses offered their guidance on physical activity and clinical issues. In Northern Ireland we hit a major milestone as we opened our Belfast Octopus trial, for progressive MS which received some fantastic coverage and paved the way for some exciting research trials over the next few years. In Scotland, we submitted a response to the latest part of the Independent Review of Adult Disability Payment (ADP), and we will continue working closely with the Scottish Parliament on this review to make sure our community’s voice is heard. In Wales, we worked closely with the new NHS Executive on the new National Strategic Clinical Network for Neurological Conditions. This aims to improve the quality, safety and sustainability of supporting services.

We also shared some disappointing news about our MS-STAT2 trial at ECTRIMS, the world’s largest annual MS research conference. Despite earlier findings to the contrary, Simvastatin didn’t slow disability progression. However, the trial has provided insights into the biology of progressive MS. Our mega-trial Octopus fully recruited its stage one participation ahead of schedule – a fantastic response from the MS community. The aim is to recruit up to 1,500 more people in the second stage.

Earlier in the year, we were honoured to partner with The Royal Opera House and The Royal Ballet. Twenty people with MS attended a series of dance workshops with choreographer Bim Malcomson, and then presented their interpretation of Cathy Marsden’s ‘The Cellist’, a ballet based on the life of renowned musician Jacqueline du Pré OBE, who lived with MS. This was an incredibly inspiring experience for all involved. We also participated in MS Awareness Week, where six MS charities and support networks came together to help raise awareness of MS. The #MSunfiltered campaign highlighted some of the more embarrassing aspects of living with MS, and recognised some of the challenges that people sometimes find difficult to share with their friends, family and healthcare network.

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Our Stop MS Appeal continued to raise money for this vital research and celebrated its penultimate year with some memorable events. These included SMS Battles, a spectacular gala quiz night, where guests were entertained by Victoria Coren Mitchell and Sue Perkins and a host of other high-profile guests, and raised over £225,000, and our carol concert in December also raised over £140,000. We were delighted that so many individuals and groups chose to support us by either donating to our Appeal or other areas of the charity by, for example, running marathons, jumping out of planes and tackling the 10in10 Peaks challenge. The passion we see from our fundraisers is always so humbling.

The MS Society Board benefits from a dedicated team of Trustees, over half of whom have joined us in the past two financial years. The focus of the Board has been on supporting and challenging the Executive as the ambitious Transformation Programme is implemented and the new Strategic Plan is developed. Behind the scenes we’ve been crafting a new committee structure and recruiting additional members to strengthen further the important governance work they do.

Finally, I would like to remember and recognise the incredible contribution Dave Myers (of Hairy Bikers fame) made to our charity, as a long-term supporter and more recently as an MS Society Ambassador. Dave, who grew up caring for his mum, who had MS, supported many of our fundraising events, and raised both awareness of MS and the impact of living as a young carer. He sadly passed away in March 2024, and we’ll always be so grateful for everything he did to help us and those who live with MS.

Professor Sir Paul Curran,

Chair, MS Society

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Our 2024 Report

In the final year of our Every MS Story strategy our latest annual report shows we have made real progress against the ambitious agenda we set ourselves. During the year our incredible staff, supporters and partners have continued to work to improve the lives of those impacted by multiple sclerosis. We believe united we can achieve much more working with people in the community who truly know the impact of living with MS and what it means. This year our community have helped us understand what services they need, what are the priorities and concerns they want us to help amplify for them, and how they want us to communicate with them.

Although we are proud and celebrate the progress and achievements of the past year, we know there is more to do, and we are determined to continue our work to achieve our vision of a world without MS.

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OUR GOAL

People living well with MS

Supporting people living with MS, and their carers, families and friends

We want people with MS to live well with their condition. We’ll continue to expand our range of services to help people understand their rights and manage their condition. And to do the things in life that are important to them.

Progress made in 2024

Our national MS Helpline continues to support as many people as possible to live well with MS. The satisfaction scores for the MS Helpline and the associated services remain high.

These include specialist support from MS nurses, physical activity specialists, benefits, employment and legal advice, and a befriending service.

In 2024 we completed the sale of our Belfast Resource Centre to the charity Sense. And the refurbishment of the centre is underway. We’ll move back into the centre in 2025 as tenants, delivering the same high-quality services in the refurbished space. We also spent much of 2024 exploring potential partnership opportunities with Sense, including joint work around carers.

In Wales, we delivered two externally funded projects. These were high-impact and taught us a lot, which we hope to scale across the network. The Breathing Space project provided support to over 300 carers with respite and short breaks, achieving its target over six months early. The Community Connections project is funded by Wales and West Utilities. This project will work across Wales and the Southwest of England, offering tailored navigation support to people affected by MS.

Our programme of Living Well virtual events delivered 53 virtual sessions, featuring lived experience volunteers, expert partners and speakers. These included webinars, peer groups, and wellbeing courses, covering key topics like Diet and MS. It also covered our newly launched Managing Stress and Anxiety with MS course. Participant feedback was overwhelmingly positive, with 97% feeling more informed and 90% planning to act on what they learned. By expanding our offerings and fostering engagement, we continue to empower people with MS with knowledge, support, and practical tools to improve their wellbeing.

Through our service transformation project, Project Mead, we are seeking to transform the services and support we provide to enable people to live well. In 2024 this involved us listening and engaging with our community about how they accessed our services now and how we could improve their experience and outcomes. From this, coming in 2025, we'll transform our national services with greater promotion and clarity about what we do, easier and clearer ways to access those services and a more relational approach to supporting people through the services they need.

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Throughout the year we continued to deliver our cost of living grants, providing vital support via our local group network to individuals in need of financial support. And we saw very positive feedback for our befriending service, which grew in 2024, providing nearly 600 sessions to 60 individuals.

Access to responsive treatment, care and support

We want to make sure everyone with MS has access to treatments, care and support needed to live their lives to the fullest, without barriers. They need to meet their needs in a way that works for them, and in a place that works for them.

Progress made in 2024

In 2024, we worked to make sure people with MS could access the treatments, care and support they needed. We campaigned to make sure people with MS can access the treatments they need. And we spoke on how to improve care and support for people with MS as part of the consultation into the NHS 10-year plan. We supported healthcare professionals through our Professional Network. They took part in a series of webinars to learn about best practices and received regular newsletters. There are now nearly 700 professionals in our network.

In October, the UK Government and NHS launched Change NHS. This was to start "the biggest ever conversation" about the future of the NHS in England. And shape the Government's 10-year Health Plan which will be published in spring 2025. The plan focuses on three big "shifts" in healthcare:

  1. moving more care from hospitals to communities,

  2. making better use of technology,

  3. preventing sickness, not just treating it.

In our consultation submission, we shared our most recent evidence and insights from our community and policy recommendations to improve the NHS in England. If introduced, our policy recommendations would support people with MS to get the right care at the right time. No matter who they are, where they live or their circumstances.

We worked to make sure treatments were available to people with MS. In 2019, Wales was the first country in the UK to approve the routine use of Fampyra on the NHS. Since then, we’ve been advocating for its availability across all Health Boards in Wales. Only one Health Board wasn’t providing the drug to people with MS. And we campaigned for the Welsh Government to make sure it became available, which it did in May 2024.

Having MS inevitably means going to the hospital, whether for diagnostic tests, routine appointments or urgent care. However, we know that sometimes it’s better to have care in the community or closer to home. This autumn, we launched our hospital admissions research project. The project helped us better understand why people with MS are going to the hospital and their experiences. And if more could be done to improve the healthcare experience of people with MS when going to the hospital. We’ll use these insights to help shape how we support NHS best practices across the UK. And to shape the asks we call for in plans for the NHS.

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We also worked to support the rollout of the updated MS optimal pathway. It sets out care and support for patients with MS. It aims to support them from their first appointment with their GP through every step of their journey. The updated pathway was published by the National Neurological Advisory Group in July 2024. We updated the information on our website at this point and promoted our Professional Network membership.

Throughout the year we also promoted the optimal clinical pathway for neurorehabilitation to local health systems and health care professionals. We delivered four webinars to share information and good practice with healthcare professionals. We also led a steering group to oversee the development of regional roundtables for 2025. The roundtables will aim to encourage and enable Integrated Care Systems (ICSs) to review their service provision. And to identify both local activity and national policy drivers enabling services to move toward the optimal pathway.

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OUR GOAL

Connected communities, powerful voices

Connecting MS communities across the UK

We don’t want anyone to feel alone, overwhelmed or misunderstood. We want to help people find and create supportive communities that are right for them, whether they exist locally or online. In doing so, we’ll increase the ways people can share experiences, tackle common issues, foster friends, build confidence and reduce isolation.

Our volunteer groups play an important role in connecting our community. We aim to provide the tools, training and resources to support our volunteers. And make sure their work is recognised and valued. To engage with all parts of the MS community, we recognise we need to create a more diverse volunteer base. We also need to develop new light-touch opportunities for people to get involved in our work.

Progress made in 2024

The main aim of our connected community is to support our 230 groups across the UK. Significant work was done this year to make sure groups can continue their excellent support and services. These are provided to tens of thousands of people affected by MS, making sure groups are safe, compliant, impactful and welcoming.

Exciting developments led by our development teams also happened across the four nations. These teams run a programme of year-round listening events to make sure the MS community is at the heart of everything we do. Projects included one with the Walton Centre in Liverpool to establish a volunteer-led help desk service. This saw them work within an NHS service to provide advice, guidance and support. The project has been a huge success so far. And similar projects aim to make sure any learning is shared and scaled where appropriate across the UK.

Through the work of our service transformation project, Project Mead, we are seeking to support more people in the MS community, through a range of community-based offers and connections. We commissioned research in the autumn of 2024 that showed people affected by MS continued to appreciate and value face-to-face connection, however, there were challenges to overcome, including transport and accessibility. In 2025 we intend to launch a new community offering, addressing what our community has told us and building on the excellent work our groups do now but offering more ways to connect. This will include the relaunch of our Near Me map on our website, so people can find the group or event that works for them.

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Developing policy positions, campaigning nationally and locally on key issues, and improving understanding of MS

MS is different for everyone, and many symptoms are invisible. People living with MS often face barriers and challenges in everyday life. We’ll raise awareness and increase public and political understanding of the realities of MS.

We want to support MS communities to become movements for change on issues affecting them. We’ll help people affected by MS to develop the skills and confidence to speak up on issues they care about. And we’ll provide the tools people need to run campaigns that bring about real change.

Progress made in 2024

In 2024 we focused on getting better insight into the number of people living with MS across the UK. We now know over 150,000 people live with MS in the UK, an increase since our last estimation. There might be a range of reasons why the number has increased, including better diagnosis and treatment. But there isn’t evidence suggesting this is because there’s an increased risk of developing MS.

We also worked to make sure the voices of people with MS were heard during the General Election with our MS Manifesto. And we delivered our open letter to Kier Starmer in the summer to speak up for MS. Once the new Government was in place, we worked to build relationships with new MPs and gather support to re-establish the APPG for MS.

Before calling the election, the previous UK Government announced a consultation into PIP with the intention to end "sick-note culture". And to potentially cut support to hundreds of thousands of disabled people. We fed into the consultation and reassured our community that changes in a Green Paper would need further consultation. And reminded people these proposals weren’t confirmed or going to happen immediately. We’ve also continued influencing Government policy on employment and financial support.

At the end of the year, the UK Government announced the first-ever UK-wide Neuro Forum. Alongside others, we’ve been calling for this forum to be set up for several years. And it was one of our big asks on healthcare in our MS manifesto and as part of the Neurological Alliance’s #BackThe1in6 campaign. This Neuro Forum is a step forward for the 1 in 6 people in the UK living with a neurological condition, including people with MS. It’ll address gaps in treatment and improve access to support and services. And we’ve been involved in supporting its set-up with the Neurological Alliances across all four nations.

In April 2024, we celebrated a campaign win. The Carer’s Leave Act became UK law, bringing in new rights for unpaid carers who work. Before this, unpaid carers didn’t have a right to time off from work for caring responsibilities. The Carer’s Leave Act gives unpaid carers the right to up to five days' unpaid leave from work for their caring responsibilities.

The UK held a general election in July 2024. We brought together our community to make sure MS was a priority for whichever party took office. Our General Election Co-production Group helped make sure our work was rooted in the priorities of people living with MS. This shaped our manifesto and the big asks we had for the next Government. We worked with our campaigners across the country, gathering signatures for our open letter to the next Prime Minister. We emailed parliamentary candidates and provided resources for volunteers for conversations with candidates on the doorstep. Before Sir Kier Starmer gave his speech outside Downing Street, we asked our MS community to sign our open letter calling for the

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Government to make MS a priority. In August, our efforts resulted in delivering over 13,000 signatures to Number 10 to speak up for MS.

We contacted over 400 new MPS, offering trusted and expert insight into what it’s like to live with MS. And how MPs can support our community. We also attended the Labour, Conservative, Liberal Democrat and Plaid Cymru party conferences. We asked our community which issues were a priority for us to share with MPs and Senedd members. We were delighted when the All-Party-Parliamentary Group for MS was re-established at the end of 2024. This sent a clear message that parliament recognises the importance of tackling the challenges people living with MS face.

Since the election, we've shared the insight and experience of our community with the Government to help shape their legislative programme. On employment, we’ve joined several roundtables with Ministers from the Departments of Work and Pensions (DWP), Health and Social Care (DHSC) and Justice. This is to bring charities, professional bodies and businesses together to talk about the Employment Bill and the changes the Government want to make to sick pay. We’ve welcomed proposed improvements such as sick pay eligibility starting from day one of employment. And the removal of the waiting days so you don’t have to be sick for several days before you can receive sick pay.

But there’s still more to do. For example, raising the rate of sick pay. And allowing phasing in and out of sick pay to support people with fluctuating conditions such as MS. This would replace the current system of stopping work when they could be better supported to stay in work for longer. This is also a challenge we’ve been tackling with our employment project. This aims to better understand the barriers to getting and staying in work for people with MS.

Financial support through Personal Independence Payments (PIP) in England and Wales and Adult Disability Payments (ADP) in Scotland are often a lifeline to people with MS. We’ve long been calling for improvements to both systems. These changes would be mindful of the fluctuating and life-long progressive nature of MS. Changes could include; removing the 20metre rule about the distance someone can walk, the 50% rule about whether an impairment impacts your life more or less than 50% of the time, and the frequent need for reassessment of any awards – something we achieved through our campaigning in Scotland with the reintroduction of indefinite awards under ADP.

In Scotland, we were involved in the Scottish Government’s Independent Review of ADP. And we responded to the interim report published in November 2023. We were pleased to see mention of improved application support and a simplified and faster application process. Because we campaigned, the Scottish Government ran a consultation on the mobility component of ADP. And guaranteed the MS Society’s involvement in the wider Independent Review of ADP. The final ADP review is due in July 2025. The next stage will involve more detail, particularly around eligibility criteria. We don’t believe in unfair assessments. And we’ll continue to campaign for changes to ADP to make sure people living with MS get the support they need.

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OUR GOAL

Effective treatments and preventing MS

Deepening our understanding of progression and improving our understanding of risk factors

The cause of MS is still unclear. But we want to understand the possible risk factors better, so we can develop ways to prevent people developing MS.

For people living with MS, not knowing how their condition will change over time is a huge challenge. We’ll be prioritising our work with UK and international partners to improve our understanding of how and why MS gets worse.

Progress made in 2024

Our researchers made exciting progress in understanding the biology of MS, uncovering potential new ways to treat it.

Our two Centres of Excellence are halfway through their five-year awards and are performing exceptionally well against their objectives. They’re world-leading Centres studying the biology of myelin repair and nerve damage in MS to find treatments to slow or stop progression. Both Centres made encouraging discoveries last year:

Early in 2024, we launched two new Doctoral Training Centres aimed at finding effective ways to manage MS symptoms without drugs. The Centres, based at Glasgow Caledonian University and King’s College London, will provide high-quality research training for 11 PhD students.

Our brand-new UK MS Prevention Taskforce worked hard during 2024 to stimulate research into MS risk reduction and prevention. The group consists of academics working in MS and related diseases, as well as people living with the condition. The group is focusing its work on three key themes:

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We opened a call for research to explore the understanding and perceptions of people with MS and their relatives. Applications are being funded in the first quarter of 2025 and this work will inform our future communications on this sensitive topic.

The Taskforce also submitted a position paper for publication outlining their work to the academic community. We’re working with MS Societies internationally to contribute to a global initiative on prevention.

In July, we brought scientists, clinicians and healthcare professionals together for our research conference, MS Frontiers. Over two days we heard from over 50 speakers, from PhD students to world-leading experts. Feedback for the event revealed that 100% of delegates said they would recommend the conference to a colleague.

Drafting of the three-year progress report for our first Equality, Diversity and Inclusion (EDI) in MS Research Action Plan is currently underway. A consultation with academic reviewers is scheduled for the first quarter of 2025 to make sure the evaluation is thorough. In 2024 we did a detailed 'theory of change' exercise. This will inform the next step of the action plan, helping us to identify the more impactful activities for 2025 and beyond.

Clinical trials programme

We believe we can slow, stop or, one day, even reverse the effects of MS, for everyone. For a charity of our size, we partner with other organisations to fund an impressive number of clinical trials aiming to find new MS treatments. A key focus of our programme is funding Octopus - a first-of-its-kind clinical trials platform with the potential to develop treatments for progression up to three times faster.

Progress made in 2024

After a decade of hard work, our Octopus trial opened its doors to people with progressive MS in 2023. We’re pleased to share the news that our Octopus trial recruited more than 375 people with MS to the first stage of the trial. We’ve reached this goal two months early, thanks to an incredible response from the MS community and the hard work of our Octopus trial sites.

The trial will now move seamlessly into the next stage, aiming to recruit up to 1,500 more people with MS. In this stage, Octopus will continue to test the same treatments: metformin and alpha lipoic acid.

In September 2024, the results of the MS-STAT2 trial were announced by Professor Jeremy Chataway at the ECTRIMS research conference in Copenhagen. The results of the MS-STAT2 trial showed simvastatin can’t slow disability progression in people with secondary progressive MS. This was disappointing news for participants, the trial team and people living with MS.

However, the trial built upon the phase 2 study to give us a definitive result. It’s collected rich information on almost 1,000 people with progressive MS, greatly increasing our understanding of the underlying biology. The trial also enabled the UK MS academic community to deliver high-quality, large-scale clinical trials, undoubtedly contributing to the success of Octopus.

Several of the other clinical trials we fund reached big recruitment milestones in 2024:

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approach. We’re also funding a long-term extension of this trial using the UK MS Register. The researchers will be able to see if starting early treatment with high-efficacy therapies can slow down the worsening of disability. This will happen using remote assessments in people’s own homes.

New Research Strategy 2025-2029

During 2024, we worked closely with our Research Strategy Committee to review progress and impact realised from our existing Research Strategy. We considered the current and future landscape of MS research and agreed high-level priority themes. The final version will be approved in 2025 by the Board of Trustees and then disseminated to our community.

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ENABLING OUR GOALS

Deepening our engagement, growing our income, and improving how we work

Deepening our engagement and growing our income

We need to grow deeper, stronger, and more enduring relationships with the MS community. We also need to provide an integrated range of services and a personalised and seamless journey, increasing the levels of financial and non-financial support.

Progress made in 2024

Engagement and awareness of the MS Society

In 2024 we launched a new symptom awareness campaign to help increase awareness and understanding of MS. We also targeted the campaign to highlight our MS Manifesto as part of the buildup to the general election. As part of MS Awareness Week earlier in the year, we joined five other MS charities and groups to launch a collaborative campaign, #MSfiltered. The campaign focused on promoting the embarrassing challenges that come with living with MS that some people have difficulty talking about. After the general election, our focus moved into our research, and the possible treatments available to the MS community. This ended with our History Makers campaign. This celebrated the diverse network of our community who contributed to making history with our research trial programmes.

We measure our engagement through indicators like awareness levels and website visitors. We saw some decline in the numbers in 2024. Although it’s difficult to be certain, we think the noisy external environment and changes to Search Engine Optimisation (SEO) are likely to be the main drivers. We’re developing a series of measures through our transformation programme and a more integrated approach to address these challenges.

Growing our income

The external financial environment remains challenging. So, we are incredibly grateful to our community for their continued financial support.

Our total income increased moderately in 2024 due to a series of successful fundraising events, one-off donations and legacies. Our Stop MS Appeal hit £90m by the end of the year, on track to achieve £100m by the end of 2025.

Some areas of fundraising remain challenging. To secure long-term growth we successfully piloted new activities like face-to-face fundraising and retail.

Improving how we work

We strive for excellence in what we deliver and how we deliver it. We recognise this can only happen by continuously evolving and reacting to internal and external environments.

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Progress made in 2024

We started 2024 by launching a bespoke leadership and management development programme. This was created to make sure all our people leaders had the skills to support staff with wider transformational activity. And within a changed employment landscape. Ninety-five people leaders were enrolled in April 2024 and attendance across the four modules reached 90% or more. Remaining and new managers joined the second cohort in the autumn of 2024.

We developed internal Safer Recruitment training in collaboration with our Safeguarding lead to support our safeguarding practices. We made this a mandatory requirement for all recruiting managers.

We updated our Pay structure and developed a Pay and Reward Policy. This provides a simplified pay structure with clarity and consistency for pay and allowance determinations. This was the first review since 2009 and was part of our wider modernisation and transformation activity and with external professional support. We’re confident this further embeds our commitment to fairness and equality across pay and allowances for our staff.

Transforming the way we'll work

Our transformation programme which includes four connected projects, will help us evolve to meet the needs of the MS community and also our future aims. These projects are:

  1. Project Bowie (Engagement and Income Generation) - designed to build income and public support through refreshing our brand, engaging more people with personal, tailored journeys and expanding the ways they can campaign, volunteer and support us financially.

  2. Project Mead (Services and Support) – designed to build up our service offer by tailoring people’s journeys, updating how we talk about our services, expanding and connecting our services and adapting to meet changing needs.

  3. Project Sage (Data and Technology) – designed to build up our data skills by connecting our data together, sharing access safely and empowering teams with data insight.

  4. Project Penguin (Culture) – designed to build up working culture by developing strong, inclusive values, showcasing ourselves to attract the best talent and building a stronger team and continuously improving our ways of working.

We know it’s a programme of scale, but we know it’ s necessary if we are going to meet our community’s needs, inspire action and build a future-proof organisation.

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OUR SUPPORTERS AND OUR COMMITMENT TO THEM

Our supporter promise

Supporters like you make a huge difference to the lives of everyone affected by MS. We want our journey together to be rewarding and enjoyable. This is our promise to you.

We promise…

To listen to you and respect your wishes

To respect any personal information, you share with us

To be accountable and committed to the highest standards

We’re registered with the Fundraising Regulator

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To be available

Fundraising Best Practice

We seek to uphold the very best in fundraising practice. Our commitment to delivering our promise is underpinned by a regular independent audit of activities. We’re also proud to be organisational members of the Fundraising Regulator. And we follow the Fundraising Preference Service’s core principles.

From time to time, we use commercial organisations to supply a specific service. But this is only when it’d be difficult or expensive for us to do an activity ourselves.

For example, in 2024, we used commercial organisations to:

To make sure suppliers are doing these activities on our behalf effectively, we have:

We always aim for the highest standards in our fundraising practice. But we might get complaints if we fail to meet these standards.

In 2024, we received 31 complaints about our fundraising activities as well as 51 complaints that were non-fundraising related.

Complaints are handled following our complaints policy. Our Supporter Care team regularly reviews complaints. And, where necessary, use the information and feedback to learn from mistakes and work with teams across the organisation to make improvements.

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Our outgoing Strategy

Every MS Story – a reflection

Our previous strategy helped refine our focus and created a strong foundation of progress. It also helped us understand the most important areas and issues for people living with and affected by MS. And where we can help make a difference. We’re incredibly grateful to everyone who’s contributed to our Every MS story strategy and the work that’s been achieved from it.

We made great strides in working to find effective treatments for people with progressive MS, as well as understanding more about MS as a condition. We broke down barriers around how people could participate in clinical trials. We diversified our trial criteria to understand more about the impact of MS across the four corners of the UK. And we made sure our research community remained fully funded and supported to continue their vital work.

Our MS Helpline and support services continued to help people live well with MS. From newly diagnosed people to employers wanting to support staff living with MS, they provided vital advice and assistance. We piloted new service offers and partnered with local and national services across the country to make sure we provided tailored support to people needing it the most.

We continued connecting people through our incredible network of volunteers, services and activities. These connections combated isolation and created strong connections and conversations with people who understood. This connection was offered to anyone affected by MS. We recognised our support needs to go beyond the individual to make sure healthcare professionals working with the MS community felt supported by us and so they felt fully informed. We also made sure decision-makers knew the impact of MS. And how they could improve access to care, support and local health services.

We’re incredibly proud of the progress we’ve made to continue our mission of transforming lives and stopping MS. But we know there’s more to do. So we’ll continue this work in our next strategy. We also know we couldn’t have done all of this without the dedication of our staff, the passion and drive of our volunteers and our community. And the generosity of our supporters. Thank you to everyone who’s been part of our journey towards our vision of a world free from MS.

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Our New Strategy

2025-29

With our UK MS community, volunteers and staff, we’re building on the progress we made in our previous strategy, Every MS Story. In our new strategy, we’ll deepen our connection with the MS Community to achieve our vision of a world free from MS. We’re setting our strategy around three main pillars, with two enabling strategic focuses. These will maximise how we can help people to live well with MS. And continue our ambition to find effective treatments and symptom management solutions for everyone.

1. Stop MS

We want to deepen our understanding of MS and so we’re developing new treatments and symptom management solutions. These drive us towards our ambition of helping people experience slower disease progression. And to help people feel more in control of their condition.

In 2025 we’ll fund research on attitudes to risk and prevention, as well as develop and launch a commissioning brief to contribute to advancing MS prevention research. We’ll also continue plans to ensure the delivery of the next stage of our mega-trial Octopus.

2. Live Well with MS

We want to continue supporting people living with MS to live well. And continue providing the best and most up-to-date information so we can unite. And work together to navigate the challenges living with MS may present. Everyone’s experience of MS is unique. And we want the MS community to feel fully supported, empowered and confident to manage their condition. We want to help create opportunities for connection and conversation. We want people to lean on their MS community and services, so no one has to face their condition alone.

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In 2025 we’ll continue supporting people living with MS by running a number of online and in-person stress and anxiety courses across the UK, providing more support through our helpline services, and continuing the success of the short breaks to unpaid carers in Wales. We’ll work closely with Sense in Northern Ireland to establish a great working partnership to ensure we continue to provide support and care to everyone affected by MS in Belfast and beyond. We’ll develop and launch a test and learn pilot to provide MS Navigation services in Wales and in South West England to help people living with and affected by MS access the right care and support they need as we know each person’s journey is unique.

3. Be Heard

We want to raise more awareness of MS in the UK and beyond. We want to shape policy and push for improvements in health and care services so that people with MS get the care and support they deserve.

In 2025 we’ll continue to amplify the voices of people living with MS and make sure we are speaking to the decision-makers who can make change happen. We plan to hold a number of parliamentary events in every nation to engage further with local government and MPs to help support our ambition to improve the services and support in the UK for people living with MS as well as their families. We’ll gather and share useful data to underpin our campaigns to raise awareness and understanding of MS in the UK. We’ll also ensure we are responding to and working with local and national government proposals around employment, sick pay, health and social care.

4. Engaging with our supporters and raising vital funds

We'll continue to engage with our supporters, providing useful and engaging content which will help amplify the lives and experiences of people who live with MS, share the latest information on available treatments, information and support for people who live with MS as well as those who support them. We'll continue to focus on raising the funds needed to support the ambitious work we have outlined, and look to attract more financial supporters, with great fundraising opportunities which will deepen their long-term financial commitments to us.

In 2025 we'll aim to achieve our Stop MS Appeal target of £100 million which will fund essential research into understanding MS and also how to stop the progression of MS. We'll look to bring in more online platforms and channels to help give donors and fundraisers more ways to support us and look at how we can expand our pool of financial supporters through test and learn pilots across all our existing communication channels as well as trialling more paid channels including paid media such as Out of Home billboards. We'll focus on optimising every communication opportunity and use some key moments across the year to push MS into the spotlight in the UK. MS Awareness Week and World MS Day will be big moments for us as well as driving more promotional activity to promote our Stop MS Appeal and our ambition to achieve our £100m target. We will also look to increase the promotion of all services and support that we provide through an integrated services promotion campaign, focusing on promotion sites in hospitals and clinical care settings.

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5. People

We want to build a strong united workforce, with smarter systems, to help us improve our ways of working to make sure we are able to deliver on our goals and ambitions to support everyone in the UK who lives with or is affected by MS.

In 2025 we want to improve our support for our volunteers through new policies, best practice guidance and management procedures. We'll look into how we can ensure those who choose to share their stories and experiences with us are supported, and how we can make sure their thoughts and advice are embedded into how we shape our services and other areas of support. We want to embed new systems including a new customer relations management system which means we'll be smarter with our conversations with our supporters, service users and donors. We'll run more training and support modules to help empower our staff and build confidence from within, so we are united and work as one team to achieve our objectives and goals.

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Finance review

Income

Overall income was 8% higher in 2024 compared with 2023. (£29.8m in 2024 compared with £27.7m in 2023). Our most significant source of income is still legacies.

Whilst this growth relied on some one-off unexpected sources including the sale of our Northern Ireland offices of £0.8m, it’s positive to have a stable financial position in a difficult external fundraising environment. There were also two areas of significant growth. Firstly, we received an additional £1.0m in legacies. Secondly, we increased income from our events, particularly The London Marathon and May 50k.

Donations

Thousands of people continue to come together to take part in fundraising events for us ensuring we can raise the funds needed to continue our work supporting people with MS in the UK.

Donations received in 2024 were at a similar level as the prior year. Lower donations from trusts were offset by higher income from our community and events.

The Medical Research Council awarded us a generous grant of £0.5m towards our Early Career Researcher projects. We were also donated a warehouse, which went on to sell for £0.6m. This gave our income a healthy boost to fund MS research through the Stop MS Appeal.

We’re working together with Wales and West Utilities for the first time. They awarded us £0.2m to fund our 18-month Community Connections project. This will connect people living with and affected by MS across Wales and Southwest England with services, activities and resources, enabling them to live well with MS.

Legacies

After a dip in legacy income for 2023, 2024 was a better year with legacy income at £14.1m (2023: £13.1m). We are hugely grateful to the many generous MS supporters who were kind enough to include a gift in their will to support our ongoing work.

Income from charitable activities

Income from charitable activities rose to £1.1m (£0.9m in 2023).

Other trading activities

In 2024, income from other trading activities rose to £1.8m (£1.5m in 2023) with the increase being because of a celebrity quiz evening held during the year.

Part of this increase resulted from nearly 600 people attending our celebrity quiz, SMS Battles, and Carols by Candlelight events, which together raised £0.4m. We were delighted to have MetLife UK return as headline sponsor for the carols.

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Expenditure

Expenditure rose by 7.8% to £32.8m, compared with £30.4m in 2023.

Raising funds

We spent £10.2m on raising funds in 2024, up from 2023 (£9.3m). The increase in expenditure was due to:

Living well with MS

Included within this category is our MS Helpline and services we provide directly to people affected by MS, either centrally or through our local volunteer groups. Further details of our work in this area can be found in the goals section of this report.

Expenditure was similar to 2023 at £8.0m (£8.0m in 2023).

Connected communities, powerful voices

Included within this category is our spend on campaigning and influencing on behalf of people affected by MS. Alongside this, we are also helping to support MS communities to become movements for change on issues that affect them.

Expenditure rose to £7.7m in 2024 (£7.3m in 2023). This increase relates to work undertaken to transform our service proposition so that we can better meet the needs of the whole community and our policy and advocacy work during an election year.

Effective treatments and preventing MS

Most of the expenditure in this area relates to research both into looking for effective treatments and in preventing MS. In 2024 we spent £6.8m a considerable increase on the £5.8m we spent in 2023. The increased spend coming from research grants with £5.9m committed in 2024 compared to £4.9m in 2023.

The spend includes £1.9m grant monies on our clinical trials programme (Octopus).

Transforming how we work

Our strategy recognised that we had to change to be efficient and remain an ally to the MS community into the future. In 2024, we have continued with a transformation programme which will improve:

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We shall transform in a structured way so that we maximise this significant investment opportunity. The cost for these investments is allocated across the strategic goals.

Sale of assets

During the year we sold and leased back our offices in Northern Ireland to the charity Sense.

The profit on sale of the assets amounted to £795k (2023:£Nil).

Our reserves

Primarily, reserves are held to enable the continuity of services and activities that we undertake to meet our strategic goals, both now and in the future.

Reserves are held for the following reasons:

In considering the level of reserves that should be held, we test the policy level against various scenarios to ensure an adequate level of reserves are held.

Given the activities we engage in, reserves do not need to be held to maintain working capital.

We have two designated funds:

  1. A fund which represents the net book value of unrestricted intangible and tangible assets.

  2. A designated fund for research. This fund was created to build reserves to enable the commitment of expenditure towards our clinical trials programme.

The MS Society has total funds of £13.6m (2023: £15.8m) with £2.6m (2023: £2.2m) within the designated fund for fixed assets, £13.3m (2023 restated: £13.2m) held in the designated fund for research, £6.1m (2023 restated: £7.8m) held in general funds and negative £8.5m (2023 restated:-£7.7m) in net restricted funds. The restricted funds also include £0.3m of endowments funds (2023: £0.3m).

Included in the -£8.5m (2023 restated: -£7.7m) of net restricted funds are negative restricted research fund balances totaling £13.3m (2023 restated: £12.9m). These negative funds are held in the expectation that specific income will be received for these projects. Given how much we raise each year in restricted research donations, part of the deficit in fund balances will be made up from donations received. Where this doesn’t happen, we also have a designated fund for research that will be used to make up the deficit (2024: £13.3m, 2023 restated: £13.2m). Therefore, we are satisfied that the deficits on negative restricted research funds will be reversed in the future.

In calculating reserves held, we include the balance of the designated fund for research after any negative restricted research balances, as these funds are available to Trustees to

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be spent as they see fit. Restricted funds are not included in reserves as these funds can only be spent in line with what the donor has specified.

Our long term aspiration is to maintain reserves within a policy range of a lower limit of 10 weeks of planned expenditure and an upper limit which is calculated as follows: 14 weeks planned expenditure plus the balance of the designated fund for research included in reserves.

We’ve made a decision to operate with a lower level of reserves in the short term to enable us to invest in a number of transformation projects (see finance review section above) which include plans to help us grow our income. Our short-term reserves policy position is to keep at least 5 weeks reserves whilst we maintain cash equating to at least 17 weeks (4 months) of planned expenditure.

On the 31 December, reserves held were £6.2m (2023: £8.1m), equating to 9.1 weeks of planned expenditure (2023: 12.3 weeks) which is in line with our short-term reserves policy position but outside our longer-term policy range. We anticipate being below our longerterm policy range for the next three years while we invest in our transformation programme.

Going concern

We have set out above a review of financial performance and our reserves position. We have adequate financial resources and are well placed to manage the business risks. Our planning process, including financial projections, has taken into consideration the current economic climate and its potential impact on the various sources of income and planned expenditure. Although we have net current liabilities, the investment portfolio could easily be drawn down should working capital be required.

In the last three years we have had deficits as we have invested in our transformation projects. However, we have kept ongoing expenditure in line with income received and are therefore confident of returning to a balanced position overall in the longer term.

We believe that there are no material uncertainties that call into doubt our ability to continue. The accounts have therefore been prepared on the basis that the MS Society is a going concern.

Investment policy

Rathbone Investment Management Limited are the MS Society’s investment managers.

The main portfolio is monitored on a total return basis using consumer price inflation (CPI) plus 3% over the investment managers’ tenure. The total return in 2024 was 7.9% (2023: 7.1%).

The Strategic Implementation and Finance Committee (SIFC) has delegated oversight of the investment portfolio. Quarterly reports from the Investment Manager were issued to the members of SIFC and the investment manager attended two committee meetings in 2024. SIFC carried out a review of the investment policy, during the year, under which the managers operate.

Net investment return

Overall, in 2024, we received investment income of £413k (2023: £410k) and with a net investment gain of £798k (2023: £680k gain).

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Our socially responsible investment position prohibits direct investment into tobacco companies and provides that the investment managers should continuously review the indirect investments into tobacco to ensure that only a diminutive level is held (no more than 1%). Additionally, the portfolio should be managed in a way that seeks to favour environmental and socially responsible investments without negatively impacting returns.

Grant making policy

We award several types of grants to meet our objectives. The major types are individual support grants and research grants.

Individual support grants

Individual support grants are mostly awarded by our local volunteer-run groups although in 2024 grants were also awarded as part of a project in Wales. Our local volunteer-run groups provide financial assistance to individuals with MS, their families and carers. These grants help with a range of costs associated with living with MS, including the cost of home adaptations, mobility aids and respite care. In addition, a new grant offers supports for cost of living needs. We awarded £303k in support grants in 2024 (£276k in 2023).

Research grants

We provide awards for research in the areas of effective treatment, prevention, symptom management and service development. These grants range from small projects to large programmes, as well as PhD studentships and fellowships.

Our top research priority is finding and testing treatments to stop disability progression. We are developing treatments that could repair damaged areas of myelin (remyelination) and protect nerves from damage (neuro-protection). We actively pursue strategic research collaboration and partnerships, both as a funder and as a source of expertise and influence. In total, we spent £5.9m (2023: £4.9m) on our active research portfolio in 2024. This figure is net of any research grant write backs.

Our principal risks and uncertainties

We are committed to effective risk management as an integral part of good corporate governance. We recognise that informed risk-taking helps to improve performance, manage our threats and opportunities, and create an environment of ‘no surprises’. This enables us to get the right balance between innovation and change and the avoidance of shocks and crises. Our risk management framework provides the policy and process that enables us to manage uncertainty in a systematic, effective and efficient way.

The Board concentrates its efforts on ensuring the most serious risks are being managed effectively; those which have a high likelihood of occurring and would have a severe impact on the achievement of our strategic plans. The Board has risk appetite statements around the key risk areas and reviews them annually. These statements consider our strategy, priorities, goals, activities and controls, and articulate the parameters within which the Board feels the overall portfolio of risks are appropriate, balanced and sustainable.

Our risk management processes are designed to enable us to conclude whether the major risks to which we are exposed have been identified, reviewed and impact assessed and are within the Board’s risk appetite. Senior management reports on key risk areas, and where our operations are not aligned to the Board’s risk appetite, to the Strategic Implementation and Finance Committee quarterly, following which the Board is updated. The Board reviews

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the corporate risk register in full on an annual basis and there are opportunities for deepdives into key risk areas, as considered necessary by the Board, during the year.

Our internal auditors carry out independent reviews across the MS Society; these reports comment on the systems of internal control and the recommendations and actions from the reports are overseen by the Audit and Risk Committee.

Following changes to the Board’s Committee structure, as referenced below, the oversight of our risk management framework sits with the Audit & Risk Committee, while the Strategic Implementation & Finance Committee has oversight of management of strategic risks.

We are confident the risk framework and methodology described above enables major risks to be identified throughout the organisation.

Below are the larger risks and uncertainties that affect the MS Society, and the plan and strategy to mitigate these risks.

1. Relationship the MS community

Our work is based on the hopes and aspirations of our MS community. Together, we campaign at all levels, fund research and provide support and information. If not everything we do is guided by the full breadth of the MS community, or we do not form lasting relationships with all of the MS community, there is a risk that our work will be less relevant and impactful, and the ambitious outcomes set out in our strategy will not be achieved.

We will continue to work together with the MS community to co-produce the best solutions for people with and affected by MS. We are delivering a significant transformation programme which seeks to deliver a step-change in how we reach, engage with and develop deeper relationships with the MS community. We will transform our services, both in delivery and design to ensure we meet the needs of people affected by MS and are able to respond to the changing environment. Our ability to gather data, evidence and insights will be strengthened to ensure our decisions are informed by the community.

2. People- volunteers and staff

2024 saw continued disruption, uncertainty and stress across all parts of wider society. As this continues, we recognise there is an ongoing risk of stress and uncertainty amongst colleagues. The significant level of change being delivered through our transformation programme, coupled with ongoing shifts in how we come together as an organisation through remote and flexible working, increases the risk of disconnection and demotivation for both staff and our volunteers.

Our new organisational strategy offers an opportunity to bring everyone together behind a clear and focussed purpose and mission, and we will be maximising opportunities to bring people together during 2025, including planning and all staff conference in the autumn.

Our transformation programme includes a strong focus on improving organisational culture and the experiences of both employees and volunteers. Our people are fundamental to our ability to deliver our strategic goals and will continue to be a key focus for us as an organisation in 2025.

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  1. Sufficient financial resources to support people affected by MS and achieve our ambition of stopping MS

The economic situation in the UK and wider global instability presents an ongoing risk to income and our ability to fundraise effectively. We will continue to take a prudent approach to planning and scale our plans accordingly. We realise we could do more if additional funds become available.

We have robust reserves in place and a clear financial model to guide our investment decisions through the transformation programme. A major project within that transformation is to strengthen and diversify our fundraising and income generating capabilities.

  1. Long-term instability in the external environment continues to cause:

  2. a) increased pressure on the NHS and social care services

  3. b) increased inequality and demands on the welfare system

  4. c) challenges to our ability to achieve coverage for, or influence on, issues affecting the MS community

The health and care system continues to face unprecedented financial, workforce and capacity challenges. This has resulted in a significant backlog of people needing care. The quality of, and access to, support for people with MS also remains highly variable across the UK. Social care and welfare systems continue to face challenges, and increasing inequality, worsened by the pandemic and cost of living crisis, will increase levels of need.

We will continue to campaign on the issues that matter to the MS community. We remain in a good position to influence the debates and achieve meaningful and lasting change for people with MS. We also continue to implement our Influencing Strategy. This seeks to empower people affected by MS to advocate for their rights on the issues they care about, both individually and as a community – and for professionals to be empowered to advocate for them.

Structure, governance and management

Structure

The Multiple Sclerosis Society (the ‘MS Society’) is a charitable company limited by guarantee, registered in England and Wales (company number 07451571; charity number 1139257).

The MS Society is governed by its Articles of Association, adopted by special resolution in December 2020. Minor amendments were agreed in December 2022 to include explicit reference to our ability to undertake advocacy work and amend the terms of co-opted trustees, so these align with elected trustees (being three years).

The MS Society is registered in Scotland with the Office of the Scottish Charity Regulator as a cross-border charity (number SC041990). We are also registered as a charity (number 1256) and as a foreign company (number 006152F) in the Isle of Man, and with the Guernsey Charity Registry (CH36).

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Main purposes

The MS Society was set up with three main charitable objectives:

Membership

The Trustees and National Council Chairs are the legal members of the Multiple Sclerosis Society. Trustees and Council Chairs become members on appointment to their respective roles and cease to be members on retirement, or when they cease to hold that role.

Board of Trustees

The Board of Trustees are the charity’s Trustees and the Directors of the company. The Board is the governing body of the MS Society, providing leadership and establishing the policies, rules and procedures of the charity. The Board also ensures the effective and equitable use of the MS Society’s resources in pursuit of its objectives.

Our electorate is made up of those members of the MS community who are interested in taking an active role in our governance and wish to elect new Trustees to the Board.

The Board is made up of eight elected Trustees and two appointed positions – these being the Chair of the Board and the Treasurer. There are also three co-opted positions, which the Board can use to address specific gaps in skills and experience. Elected and co-opted Trustees serve a term of three years and may then be reappointed to serve a further consecutive term of three years, before a break of at least one year.

Reappointment is based on performance in the role and follows a robust appraisal process undertaken by the Chair or Vice Chair of the Board.

The Chair of the MS Society is selected by the Board and may serve for one term of five years. The Treasurer is appointed for a three-year term of office and may serve for two consecutive terms before a break of at least one year.

All Trustees (elected, co-opted or appointed) are recruited through open advertisement of the vacancy and a formal application and interview process.

Each new Trustee receives a comprehensive induction, emphasising the MS Society’s charitable objectives and strategic goals. This process also provides briefings on the key responsibilities of Trustees and the Board, as well as an understanding of MS and the specific needs of the MS community we are seeking to address.

Two trustees with specialist skills and knowledge of income generation and engagement were recruited to join the Board during the year.

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Trustee
attendance
2024
12
April
2024
10
July
2024
24 September
2024
11
December
2024
Prof Sir Paul Curran (Chair) 1 1 1 1
Emily Revess (Vice Chair) 1 1 A 1
Nick Keveth (Treasurer) 1 1 1 1
Bayan Mohajeri 1 1 1 1
Chris Murray 1 1 1 1
David Silver 1 1 1 1
Jason Jaspal N/A Observing 1 1
Leah Mates N/A Observing 1 1
Polly Williams 1 1 1 1
Sarah Schol 1 1 1 1
Dr. Shewly Choudhury A 1 1 1
Dr. Stephanie Wright A 1 1 1
Stephen O’Keane A 1 1 A

Board delegation

The Board delegates the exercise of certain powers in connection with the management and administration of the MS Society to the Chief Executive and their staff through the Scheme of Delegation, which is available on the MS Society’s website.

The Board also delegates oversight for specific areas to its Committees:

The Nominations and Remuneration Committee has delegated responsibility for providing oversight of Trustee appointments and elections, as well as Board succession planning and remuneration (pay and benefits) matters relating to staff, including recommending the Staff Pay and Rewards Policy to the Board for approval. It reviews Executive Director and CEO remuneration, including annual pay awards, for recommendation to the Board of Trustees, and oversees CEO appointment for recommendation to the Board of Trustees. During 2024 and in 2025 the Committee has maintained oversight of CEO remuneration only and made recommendations to the Board on annual pay awards. A new policy and process for the determination of remuneration for both Executive Directors and the CEO is being developed by the Committee for implementation from 2026.

8 Mar 2024 10 Jun 2024 29 Oct 2024
Polly Williams (Chair) Trustee 1 1 1
Sarah Schol ¹ Trustee 1 1 1
Emily Revess ² Trustee 1 1 1
Laura Ingram Councils 1 1 1
Susannah Robinson Councils 1 1 1

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The Strategic Implementation and Finance Committee has delegated responsibility for assessing and monitoring strategic implementation and financial performance. The Committee considers the adequacy of progress made in achieving strategic objectives and the effectiveness of outcomes, including impact for the MS community. The Committee reviews the systems in place to measure and monitor strategic and financial performance.

12 Mar 24 4 Jun 24 4 Sep 24 19 Nov 24
Chris Murray Chair 1 1 1 1
Nick Keveth Treasurer¹ 1 1 1 1
Bayan Mohajeri Trustee 1 1 1 1
Shewly Choudhury Trustee A 1 1 A
Jason Jaspal Trustee 1 1
Leah Mates Trustee 1 1
Lucy Tusa Independent 1 1
Philippa Donnelly Independent 1 1
Sissel Heiberg Independent 1 1

The Audit and Risk Committee has delegated responsibility for providing the Board with oversight of the MS Society’s systems for internal control, risk management, assurance and compliance including internal and external audit.

14 Mar 24 4 Jun 24 5 Sep 24 20 Nov 24
Nick Keveth (Chair) Treasurer¹ 1 1 1 1
David Silver Trustee 1 1 1 1
Stephanie Wright Trustee 1 1 A 1
Stephen O’Keane Trustee 1 1 1 1
Josie Hutchings Indep. 1 1 1 1
Neal Aggarwal Indep. 1 1

During 2024, four new independent committee members were recruited to bring specific skills and knowledge onto the Strategic Implementation and Finance Committee, and the Audit and Risk Committee.

The four National Councils provide a voice for the MS community in the nations of the UK. They also act as ambassadors and advocates for people with or affected by MS and help to deliver the MS Society’s strategy in their nation. The National Councils (Cymru, England, Northern Ireland and Scotland) provide a direct link between the nations and the Board of Trustees.

Public benefit

The senior management and Trustees of the MS Society have complied with the duty in section 4 of the Charities Act 2011 to have due regard for the public benefit guidance

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published by the Charity Commission in administering the MS Society, in determining achievements against the aims set for 2024, and in planning activities for 2025.

Section 172 Statement

In line with the duties set out in section 172 of the Companies Act 2006, the Trustees, as directors of the company, have acted in good faith – in the way they consider to be most likely to promote the success of the charity and achieve its charitable purposes. This includes placing the needs of the MS community at the heart of all that we do and focusing on insight-led decision making. Our services are co-produced with volunteers and people affected by MS.

Charity Governance Code

The MS Society has embraced the Charity Governance Code as a tool for self-assessment and continuous improvement. The Board is satisfied that we substantially comply with the Code and our performance against it is reviewed on an annual basis. In line with the Code, the Board reviews its own performance and that of individual Trustees, including the Chair on an annual basis, with an external evaluation every three years.

In 2024, Trustees were asked to complete a self-assessment survey of Board effectiveness. Overall, responses to the survey indicated that Trustees had confidence in the overall effectiveness of the Board and no significant areas of concern or for improvement were raised.

The Board as also introduced annual effectiveness self-assessment surveys for the three sub-committees, the findings of which were reported to the Board. The responses in 2024 indicated that the changes to the sub-committee structure were proving effective.

Chief Executive and senior management

The Chief Executive is responsible for the day-to-day management of the charity’s affairs and for implementing policies agreed by the Board. The Chief Executive is assisted by senior managers who lead our staff and volunteers.

Offices

We have offices in Belfast, Cardiff, Edinburgh and London.

Our volunteer-run groups

There are 230 MS Society volunteer-run groups:

Our volunteers

Volunteers are at the heart of the MS Society, making a significant contribution across our activities.

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We have around 2,700 volunteers, many of whom have a personal connection to MS. Without their commitment, we simply would not be able to achieve everything we do. Their dediction remains the cornerstone of our success in delivering our goals.

Volunteers raise vital funds, campaign for change, and share their lived experience to increase awareness of MS and shape our work. They operate our MS Helpline, inform our research, keep our charity shops running, provide services and support locally, and influence our strategic priorities as Trustees and National Council members.

We want volunteering at the MS Society to be an enjoyable and fulfilling experience. We continuously strive to improve the support and information we give our volunteers, review processes, and simplify the complexities of compliance.

It is hard to put a value on the commitment of our volunteers in supporting and advocating for people affected by MS. It is only through their generous donation of time and skills that we are able to achieve such a positive impact on the MS community. We want our volunteers to feel valued and recognised throughout each year, but Volunteers’ Week provides a particular opportunity for thanks.

In 2024, we shared a series of 10 videos across our social media channels from our Ambassadors, Chair of Trustees, CEO, staff and a service user, detailing some of the reasons we wanted to celebrate our volunteers. We also shared a TikTok video and lots of blogs from volunteers themselves, so our followers could hear first-hand about all the things they do.

Across Facebook, X (formerly Twitter), Instagram, TikTok and LinkedIn, our Volunteers’ Week posts were viewed almost 87,000 times and were engaged with (liked, commented on, shared or the link was clicked) almost 3,000 times.

We were also keen to raise awareness of volunteering within the organisation and held a Zoom session for staff to hear from two of our local groups about the services and support they offer, which was very well received.

Our employees

In 2024, our employee turnover rate increased to 25.4% compared with 19% in 2023. However, 26% of 73 leavers during this period were non-voluntary leavers – (as a result of contract endingor redundancy, TUPE or other reasons.) Voluntary turnover for 2024 was 18.8%.

We have continued to review and improve our reward offer to existing and new employees.

During the year, we also developed and rolled out a bespoke leadership and management development programme for our managers and leaders across the charity to further support their contribution and impact to all our activities and continued transformation. This development programme continues to be rolled out to all new people managers and will be supplemented in 2025 with further targeted people manager learning.

Our approach to employing disabled people

We are dedicated to being an exemplary employer of disabled people, including those people with MS. Our commitment to non-discrimination is embedded in our policies, procedures and practices.

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We make reasonable adjustments to support disabled employees to meet their full potential – by implementing best employment practices, providing equal access to learning, ensuring equal opportunity for promotion, tackling discrimination and removing access barriers, where reasonably practicable to do so.

We are also committed to ensuring all disabled employees feel confident to share details of their condition or impairment and needs with us. To that end we continue to promote completion of sensitive personal information internally, carefully explaining how and why it is used and confirming who can access this highly sensitive information.

Keeping staff informed

We have well-established arrangements for giving staff a voice in what we do and a chance to share their thoughts. We have a programme of pulse and topic-based surveys, alongside other listening events like Q&A or drop-in sessions with leadership.

We have continued to develop and adapt our communication channels to support and connect colleagues. During 2024, we offered a range of opportunities for staff to connect, engage, learn and share feedback. These included regular opportunities to hear from our leadership, projects, peers, external speakers and the MS community.

All our people have access to the Board of Trustees’ meeting summary reports, which are publicly available on our website.

Our joint negotiating and consultation committee (JNCC) – formed of union representatives, staff representatives and members of senior management – which meets regularly, also facilitated the participation of representatives within a JNCC sub-group to support the progression and development of the pay review project.

Remuneration

We aim to pay salaries that are fair and proportionate to the complexity of each role and are competitive within the charity sector. All our salaries have been externally benchmarked against the median within comparable charities and organisations.

During 2024, we completed a Pay Review Project which allowed us to design a new fair and transparent pay structure and developed a new Pay and Reward policy clearly setting out how pay and allowances are determined. We moved 22.7% of employees directly to the new pay structure in August 2024 as this was immediately beneficial to them. Other employees remained on their existing pay until an annual cost of living award and incremental progressions were applied in January 2025. As a direct result, 82.3% of employees are now on the new pay structure with all remaining staff due to transfer across by August 2025.

Our employees continue to be paid at or above the UK Living Wage (as defined by the Living Wage Foundation).

Our trustees are not remunerated. Remuneration for other key management personnel is handled in the same way as for all other staff, except for the Chief Executive. This is based on similar principles as for all other staff, but a different process is used and it is decided by the Board. Following a governance review, work has been initiated to develop a policy and process for the determination of remuneration for both Executive Directors and the CEO.

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Environmental sustainability

We are committed to environmental sustainability and the management of resources is an important issue for the charity.

The following data relates to our annual energy consumption and CO2 emissions:

Utility and Scope 2024
Consumption
(kWh)
2023
Consumption
(kWh)
2024
Consumption
(tCO2e)
2023
Consumption
(tCO2e)
214,629 183,204 12.9 11.0
Grid supplied electricity
for heating/cooling
(scope 2) where heat
pumps are used
112,975 123,976 23.4 25.7
Grid supplied electricity
(scope 2)
175,276 284,324 31.5 51.2
Gaseous and other fuels
(scope 1)
62,771 51,450 15.1 12.3
Transportation
(scope 1) buses
102,601 111,142 23.4 25.3
Transportation (scope 3)
mileage
668,252 754,096 106.3 125.5
Total
295.5 295.0 295.5 295.0
Intensity metric FTE
2,261.4 2,556.3 0.4 0.4
Kwh/FTE & TCO2e / FTE

The main national office in London uses heat pumps for heating and cooling which reduce its carbon emissions compared with say, using a standard gas boiler. For the purposes of this exercise we’ve assumed that carbon emissions are a third of the emissions created by gas. Clearly the use of heat pumps at our main office reduces our overall carbon emissions.

Grid supplied electricity is mostly to our day centres and our other offices. We have been reducing our overall office space along with transferring our remaining day centres to separate entities.

Gaseous and other fuels relate to our Northern Ireland office and our remaining day centre. The NI office was sold during the year and one of our day centres was transferred to another charity resulting is a substantial reduction in consumption.

Transportation - buses – relates to minibuses operated in our volunteer network.

Transportation - mileage – relates to mileage incurred by both staff and volunteers.

MS Society

36

Relationship between the MS Society and its subsidiaries

MSS (Trading) Ltd

The Multiple Sclerosis Society is the sole shareholder, owning two shares, in MSS (Trading) Limited, company number 02895015. The principal activities of MSS (Trading) Limited are corporate sponsorship, sale of greeting cards and sale of advertising space for the benefit of the MS Society.

MS Society Nominees Limited

MS Society Nominees Limited, company number 03667753, a company limited by guarantee without share capital, holds the title deeds of the MS Society’s property portfolio.

Multiple Sclerosis Society of Great Britain and Northern Ireland – linked charity

The MS Society is the sole trustee and sole member of the Multiple Sclerosis Society of Great Britain and Northern Ireland with a registered charity number 1139257/1 (formerly 207495), precursor of the MS Society.

MS Society

37

Statement of Trustees’ responsibilities and corporate governance

Trustees’ responsibilities statement

The Trustees are responsible for preparing the Trustees’ Report and the financial statements in accordance with applicable law and regulations.

Company law requires the Trustees to prepare financial statements for each financial year and the Trustees have elected to prepare the financial statements in accordance with United Kingdom Generally Accepted Accounting Practice (United Kingdom Accounting Standards and applicable law).

Under company law the Trustees must not approve the financial statements unless they are satisfied that they give a true and fair view of the state of affairs of the charitable company and the group and of the incoming resources and application of resources, including the income and expenditure, of the charitable group for that period.

In preparing these financial statements, the Trustees are required to:

The Trustees are responsible for keeping adequate accounting records that are sufficient to show and explain the charitable company’s transactions and disclose with reasonable accuracy at any time the financial position of the company and enable them to ensure that the financial statements comply with the Companies Act 2006. They are also responsible for safeguarding the assets of the charitable company and the group and ensuring their proper application under charity law and hence for taking reasonable steps for the prevention and detection of fraud and other irregularities.

In so far as each of the Trustees is aware:

The Trustees are responsible for the maintenance and integrity of the corporate and financial information included on the company’s website.

Legislation in the United Kingdom governing the preparation and dissemination of financial statements may differ from legislation in other jurisdictions.

During the year Haysmacintyre LLP changed its name to HaysMac LLP.

HaysMac LLP has indicated its willingness to be reappointed as statutory auditor.

MS Society

38

Approved by the Board of Trustees of the MS Society on 2 April 2025 including, in their capacity as company directors, the strategic report contained therein, and signed on its behalf by:

N J Keveth

N J Keveth (Apr 10, 2025 16:30 GMT+1)

Nick Keveth Treasurer

MS Society

39

Independent auditor’s report to the members and trustees of Multiple Sclerosis Society

Opinion

We have audited the financial statements of Multiple Sclerosis Society for the year ended 31 December 2024 which comprise Consolidated Statement of Financial Activities, the Consolidated and Charity Balance Sheets, the Consolidated Statement of Cash Flows and notes to the financial statements, including a summary of significant accounting policies. The financial reporting framework that has been applied in their preparation is applicable law and United Kingdom Accounting Standards, including Financial Reporting Standard 102 The Financial Reporting Standard applicable in the UK and Republic of Ireland (United Kingdom Generally Accepted Accounting Practice).

Basis for opinion

We conducted our audit in accordance with International Standards on Auditing (UK) (ISAs (UK)) and applicable law. Our responsibilities under those standards are further described in the Auditor’s responsibilities for the audit of the financial statements section of our report. We are independent of the group in accordance with the ethical requirements that are relevant to our audit of the financial statements in the UK, including the FRC’s Ethical Standard, and we have fulfilled our other ethical responsibilities in accordance with these requirements. We believe that the audit evidence we have obtained is sufficient and appropriate to provide a basis for our opinion.

Conclusions relating to going concern

In auditing the financial statements, we have concluded that the trustees’ use of the going concern basis of accounting in the preparation of the financial statements is appropriate.

Based on the work we have performed, we have not identified any material uncertainties relating to events or conditions that, individually or collectively, may cast significant doubt on the group's ability to continue as a going concern for a period of at least twelve months from when the financial statements are authorised for issue.

Our responsibilities and the responsibilities of the trustees with respect to going concern are described in the relevant sections of this report.

40

Other information

The trustees are responsible for the other information. The other information comprises the information included in the Trustees’ Report and the Chair’s statement. Our opinion on the financial statements does not cover the other information and, except to the extent otherwise explicitly stated in our report, we do not express any form of assurance conclusion thereon.

In connection with our audit of the financial statements, our responsibility is to read the other information and, in doing so, consider whether the other information is materially inconsistent with the financial statements or our knowledge obtained in the audit or otherwise appears to be materially misstated. If we identify such material inconsistencies or apparent material misstatements, we are required to determine whether there is a material misstatement in the financial statements or a material misstatement of the other information. If, based on the work we have performed, we conclude that there is a material misstatement of this other information, we are required to report that fact. We have nothing to report in this regard.

Opinions on other matters prescribed by the Companies Act 2006

In our opinion, based on the work undertaken in the course of the audit:

Matters on which we are required to report by exception

In the light of the knowledge and understanding of the group and the parent charitable company and its environment obtained in the course of the audit, we have not identified material misstatements in the Trustees’ Report (which incorporates the strategic report and the directors’ report).

We have nothing to report in respect of the following matters in relation to which the Companies Act 2006 and the Charity Accounts (Scotland) Regulations (as amended) require us to report to you if, in our opinion:

Responsibilities of trustees for the financial statements

As explained more fully in the trustees’ responsibilities statement set out on page 38, the trustees (who are also the directors of the charitable company for the

41

purposes of company law) are responsible for the preparation of the financial statements and for being satisfied that they give a true and fair view, and for such internal control as the trustees determine is necessary to enable the preparation of financial statements that are free from material misstatement, whether due to fraud or error.

In preparing the financial statements, the trustees are responsible for assessing the group’s and the parent charitable company’s ability to continue as a going concern, disclosing, as applicable, matters related to going concern and using the going concern basis of accounting unless the trustees either intend to liquidate the group or the parent charitable company or to cease operations, or have no realistic alternative but to do so.

Auditor’s responsibilities for the audit of the financial statements Our objectives are to obtain reasonable assurance about whether the financial statements as a whole are free from material misstatement, whether due to fraud or error, and to issue an auditor’s report that includes our opinion. Reasonable assurance is a high level of assurance, but is not a guarantee that an audit conducted in accordance with ISAs (UK) will always detect a material misstatement when it exists. Misstatements can arise from fraud or error and are considered material if, individually or in the aggregate, they could reasonably be expected to influence the economic decisions of users taken on the basis of these financial statements.

Irregularities, including fraud, are instances of non-compliance with laws and regulations. We design procedures in line with our responsibilities, outlined above, to detect material misstatements in respect of irregularities, including fraud. The extent to which our procedures are capable of detecting irregularities, including fraud is detailed below:

Based on our understanding of the group and the environment in which it operates, we identified that the principal risks of non-compliance with laws and regulations related to fundraising regulations, charity and company law applicable in England and Wales and Scotland,, and we considered the extent to which non-compliance might have a material effect on the financial statements. We also considered those laws and regulations that have a direct impact on the preparation of the financial statements such as the Companies Act 2006, the Charities and Trustee Investment (Scotland) Act 2005, the Charities Act 2011, and payroll taxes.

We evaluated management’s incentives and opportunities for fraudulent manipulation of the financial statements (including the risk of override of controls), and determined that the principal risks were related to the completeness and cutoff of voluntary income, legacies, grant income and investment income. Audit procedures performed by the engagement team included:

42

Because of the inherent limitations of an audit, there is a risk that we will not detect all irregularities, including those leading to a material misstatement in the financial statements or non-compliance with regulation. This risk increases the more that compliance with a law or regulation is removed from the events and transactions reflected in the financial statements, as we will be less likely to become aware of instances of non-compliance. The risk is also greater regarding irregularities occurring due to fraud rather than error, as fraud involves intentional concealment, forgery, collusion, omission or misrepresentation.

A further description of our responsibilities for the audit of the financial statements is located on the Financial Reporting Council’s website at: www.frc.org.uk/auditorsresponsibilities. This description forms part of our auditor’s report.

Use of our report

This report is made solely to the charitable company's members, as a body, in accordance with Chapter 3 of Part 16 of the Companies Act 2006, section 44(1)(c) of the Charities and Trustee Investment (Scotland) Act 2005 and regulation 10 of the Charities Accounts (Scotland) Regulations 2006. Our audit work has been undertaken so that we might state to the charitable company's members those matters we are required to state to them in an Auditor's report and for no other purpose. To the fullest extent permitted by law, we do not accept or assume responsibility to anyone other than the charitable company and the charitable company's members as a body, for our audit work, for this report, or for the opinions we have formed.

15/04/2025

Steven Harper (Senior Statutory Auditor) 10 Queen Street Place For and on behalf of HaysMac LLP, Statutory Auditors London

EC4R 1AG

43

Consolidated Statement of Financial Activities (SOFA) (incorporating an income and expenditure account)

Year ended 31 December 2024
Note
Income from:
5
Unrestricted

funds
Restricted
funds
2024
Total
2023
Restated
Total
£'000 £'000 £'000 £'000
Donations 7,874 3,754 11,628 11,707
Legacies receivable
Charitable activities
12,348
367
1,727
685
14,075
1,052
13,101
885
Other trading activities 1,131 680 1,811 1,535
Investment income
Other income - Profit on sale of assets
403
797
10
-
413
797
410
14
Total income
5
22,920 6,856 29,776 27,652
Expenditure on:
6
Raising funds
Charitable activities
Goal 1 - Living well with MS
Goal 2 - Connected communities, powerful voices
Goal 3 - Effective treatments and preventing MS
7,923
5,659
7,523
867
2,310
2,313
197
5,982
10,233
7,972
7,720
6,849
9,256
8,032
7,338
5,788
Total expenditure
6
21,972 10,802 32,774 30,414
Net gains on investments
16
Net income/(expenditure)
Transfers
22
Other recognised gains and losses
777
21
798
680
1,725
(2,850)
(1)
(3,925)
2,850
-
(2,200)
-
(1)
(2,082)
-
(12)
Net movement in funds (1,126) (1,075) (2,201) (2,094)
Reconciliation of funds
Total funds brought forward
24,135 (8,347) 15,788 17,882
Prior year adjustment (see note 11)
11
(907) 907 - -
Total funds brought forward restated 23,228 (7,440) 15,788 17,882
Total funds carried forward
22
22,102 (8,515) 13,587 15,788

Prior year split between unrestricted and restricted appears in note 23.

Restricted funds includes endowment funds of £310k (2023: £292k) - see note 21 for an analysis. No separate income and expenditure account is required under the Companies Act 2006 as the only difference between net income as stated above and net income as defined by the Companies Act is net income on endowment funds of £18k (2023: £10k). All activities above were from continuing activities.

MS Society

44

Consolidated and Charity Balance Sheets

31 December 2024

2024
2023
Restated
Notes
£'000
£'000
Fixed assets
Intangible assets
13
1,750
814
Tangible assets
14
1,025
1,543
Investments
16
12,688
14,620
Total fixed assets
15,463
16,977
Current assets
Debtors
17
12,020
12,082
Cash at bank and in hand
1,591
824
Total current assets
13,611
12,906
Liabilities:
Creditors: Amounts falling due within one year
19
15,393
14,033
Provisions for liabilities
20
94
62
Net current assets/(liabilities)
(1,876)
(1,189)
Total assets less current liabilities
13,587
15,788
Total net assets
22
13,587
15,788
Funds
Endowment funds
22
310
292
Restricted income funds (see the reserves policy
in the Trustees' report page 25)
22
(8,825)
(7,732)
Unrestricted funds
- Designated for intangible and tangible fixed assets
2,636
2,213
- Designated for research (Stop MS Appeal)
13,342
13,248
- General funds
6,124
7,767
Total unrestricted funds
22
22,102
23,228
Total charity funds
22
13,587
15,788
Consolidated
2024
2023
Restated
Notes
£'000
£'000
Fixed assets
Intangible assets
13
1,750
814
Tangible assets
14
1,025
1,543
Investments
16
12,688
14,620
Total fixed assets
15,463
16,977
Current assets
Debtors
17
12,020
12,082
Cash at bank and in hand
1,591
824
Total current assets
13,611
12,906
Liabilities:
Creditors: Amounts falling due within one year
19
15,393
14,033
Provisions for liabilities
20
94
62
Net current assets/(liabilities)
(1,876)
(1,189)
Total assets less current liabilities
13,587
15,788
Total net assets
22
13,587
15,788
Funds
Endowment funds
22
310
292
Restricted income funds (see the reserves policy
in the Trustees' report page 25)
22
(8,825)
(7,732)
Unrestricted funds
- Designated for intangible and tangible fixed assets
2,636
2,213
- Designated for research (Stop MS Appeal)
13,342
13,248
- General funds
6,124
7,767
Total unrestricted funds
22
22,102
23,228
Total charity funds
22
13,587
15,788
Consolidated
2024
2023
Restated
Notes
£'000
£'000
Fixed assets
Intangible assets
13
1,750
814
Tangible assets
14
1,025
1,543
Investments
16
12,688
14,620
Total fixed assets
15,463
16,977
Current assets
Debtors
17
12,020
12,082
Cash at bank and in hand
1,591
824
Total current assets
13,611
12,906
Liabilities:
Creditors: Amounts falling due within one year
19
15,393
14,033
Provisions for liabilities
20
94
62
Net current assets/(liabilities)
(1,876)
(1,189)
Total assets less current liabilities
13,587
15,788
Total net assets
22
13,587
15,788
Funds
Endowment funds
22
310
292
Restricted income funds (see the reserves policy
in the Trustees' report page 25)
22
(8,825)
(7,732)
Unrestricted funds
- Designated for intangible and tangible fixed assets
2,636
2,213
- Designated for research (Stop MS Appeal)
13,342
13,248
- General funds
6,124
7,767
Total unrestricted funds
22
22,102
23,228
Total charity funds
22
13,587
15,788
Consolidated
2024
2023
Restated
£'000
£'000
Charity
2024
2023
Restated
£'000
£'000
Charity
1,750
1,025
12,688
814
1,543
14,620
1,750
1,025
12,688
814
1,543
14,620
15,463
12,020
1,591
16,977
12,082
824
15,463
12,053
1,513
16,977
12,084
790
13,611
15,393
94
12,906
14,033
62
13,566
15,384
94
12,874
14,018
62
(1,876) (1,189) (1,912) (1,206)
13,587 15,788 13,551 15,771
13,587 15,788 13,551 15,771
310 292 310 292
(8,825) (7,732) (8,825) (7,732)
2,636
13,342
6,124
2,213
13,248
7,767
2,636
13,342
6,088
2,213
13,248
7,750
22,102 23,228 22,066 23,211
13,587 15,788 13,551 15,771

The turnover for the charity was £29.7m (2023: £27.6m) and the net movement in funds in the charity was -£2.2m (2023: - £2.1m). A charity SOFA appears at the back of these accounts.

These financial statements were approved, authorised for issue and signed on behalf of the Trustees on 2 April 2025. The notes on pages 47 to 66 form part of these financial statements.

N J Keveth

N J Keveth (Apr 10, 2025 16:30 GMT+1)

Nick Keveth Treasurer

Multiple Sclerosis Society. Registered charity nos.1139257 / SC041990. Registered as a limited company by guarantee in England and Wales 07451571.

MS Society

45

Consolidated statement of cash flows Year ended 31 December 2024

Consolidated statement of cash flows
Year ended 31 December 2024
Note
Cash flows from operating activities:
Net cash provided by (used in) operating activities
A
Cash flows from investing activities:
Dividends and interest from investments
Proceeds from the sale of property, plant and equipment
Purchase of intangible assets
Purchase of property, plant and equipment
Proceeds from sale of investments
Purchase of investments
Net cash provided by (used in) investing activities
Cash flows from financing activities:
Change in cash and cash equivalents in the reporting period
Cash and cash equivalents as at 1 January
B
Change in cash and cash equivalents due to exchange rate movements
Cash and cash equivalents as at 31 December
B
Net income/expenditure for the reporting period (as per the statement of financial activities)
Adjustments for:
Depreciation and amortisation charges
(Gains)/Losses on investments
Dividends and interest from investments
Profit on the sale of fixed assets
Decrease/(Increase) in debtors
Increase/(Decrease) in creditors
Net cash provided by (used in) operating activities
B. Analysis of cash and cash equivalents
Cash in hand
Total cash and cash equivalents
A. Reconciliation of net income/(expenditure) to net cash flow from
operating activities
2024
£'000
(2,359)
2023
£'000
(2,590)
413
1,089
(1,024)
(81)
2,981
(251)
410
14
(733)
-
4,971
(3,246)
3,127 1,416
- -
768
824
(1)
(1,174)
2,010
(12)
1,591 824
(2,200)
395
(798)
(413)
(797)
62
1,392
(2,082)
351
(680)
(410)
(14)
(1,721)
1,966
(2,359) (2,590)
1,591 824
1,591 824

Note the Society has taken advantage of the exemption contained in FRS102 on the preparation of a charity cash flow statement.

C. Reconciliation of net funds
Cash
Total
1 Jan 2024
£'000
824
Cash flows
£'000
768
Foreign
exchange
movements
£'000
(1)
31 Dec 2024
£'000
1,591
824 768 (1) 1,591

MS Society

46

Year ended 31 December 2024

Notes to Consolidated Accounts

1. Charity information

The charity is a private limited company (registered number 07451571), which is incorporated and domiciled in the UK. The address of the registered office is Carriage House, 8 City North Place, London N4 3FU.

2. Accounting policies

a) Basis of preparation

The accounts (financial statements) have been prepared in accordance with the Statement of Recommended Practice for Charities (SORP 2019) (Second Edition, effective 1 January 2019) applicable to charities preparing their accounts in accordance with the Financial Reporting Standard applicable in the UK and Republic of Ireland (FRS 102), the Charities Act 2011, the Charities and Trustee Investment (Scotland) Act 2005, the Charities Accounts (Scotland) Regulations 2006 and UK Generally Accepted Practice as it applies from 1 January 2019.

The MS Society meets the definition of a public benefit entity under FRS 102. Assets and liabilities are initially recognised at historical cost or transaction value unless otherwise stated in the relevant accounting policy note(s).

These are consolidated accounts representing the accounts of the MS Society, its linked charity 'Multiple Sclerosis Society of Great Britain and Northern Ireland' and its subsidiary company, MSS (Trading) Limited (registered company number 02895015). These accounts have been consolidated on a line by line basis.

The Society's volunteer-run groups account on a receipts and payments basis with a selection of groups required to submit an 'Agreed upon Procedures Report' (APR) which has been signed off by a Chartered Accountant.

b) Going concern

Based on forecasts and projections, the Trustees consider that the Society is well placed to manage the business risks it faces. This position is supported by a strong cash flow, reserves and relatively stable income. Over the last three years the Society has been running deficit budgets to enable various transformation projects to help us acheive our strategic aims but normal day to day spending has been kept in line with income.

Given the above the Trustees have a reasonable expectation that the Society has sufficient resources to continue for at least 12 months after the signing of the financial statements and believe that there are no material uncertainties that call into doubt the ability to continue as a going concern. Therefore the Society continues to adopt the going concern basis in preparing its consolidated financial statements.

c) Functional/presentation currency

The functional currency of the Society and its subsidiary is considered to be in pounds sterling because that is the currency of the primary economic environment in which the charity/group operates. The consolidated financial statements are also presented in pounds sterling rounded to the nearest thousand unless otherwise shown.

d) Funds

The different funds are defined as follows:

Restricted income
funds
Endowment funds
Restricted income funds are subject to specific restrictions imposed by the donor or by the nature of the
appeal.
Permanent endowment
:where a donor specifies only income arising from a donation can be used and
the income may also be restricted towards a particular purpose.
Expendable endowment
:a fund that must be invested to produce income. Depending on the conditions
attached to the endowment, the Trustees will have a legal power to convert all or part of it into an income
fund which can then be spent.
General funds /
Unrestricted funds
General funds are unrestricted income funds available to the Society for its general purposes and
include funds designated for a particular purpose. The use of designated funds remains at the discretion
of Trustees.

e) Income

All income is accounted for when the Society has entitlement, the receipt is probable and the amount is measurable.

■Legacies are recognised when all the three criteria below are met:

MS Society

47

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

2. Accounting policies (continued)

e) Income (continued)

f) Expenditure

Expenditure is accounted for on an accruals basis except for volunteer-run groups that account on a receipts and payments basis. Expenditure includes irrecoverable VAT where applicable. The Society makes research grants after evaluating the merits of each grant application and by peer review of grant applications. Each grant commitment is dependent on the satisfactory outcome of a review which, for most grants, is carried out annually. Consequently, for these grants, the Society commits expenditure up to the next date when a review will be done.

Expenditure is allocated to relevant activity categories on a basis that is consistent with the use of the resource.

Support costs consisting of human resources department (HR), facilities and information technology (IT) are apportioned based on the number of staff (full-time equivalents) working on core activities. Finance costs, governance costs and general management costs are apportioned based on direct costs on core activities.

g) Intangible fixed assets

Intangible fixed assets are included at cost and amortised on a straight line basis, in order to write off the assets over their useful lives. Assets below £5,000 are not capitalised. The only assets held as intangible fixed assets are software and costs associated with setting up a new website. These costs are amortised at 33 ⅓% in order to write off these assets over the period of time the Society will receive economic benefit from them.

h) Tangible fixed assets, depreciation and impairment

Tangible fixed assets are included at cost and depreciation is provided on a straight line basis, in order to write off the assets over their useful lives. Assets below £5,000 are not capitalised.

The depreciation rates are as follows: The depreciation rates are as follows:
Freehold land Nil Computer equipment 33 ⅓%
Freehold buildings 2% Motor vehicles 25%
Leasehold buildings Remaining term of lease Fixtures and equipment 20%

Fixed assets are subject to a review for impairment where there is an indication of a reduction in their carrying value. Any impairment is recognised in the Consolidated Statement of Financial Activities in the year in which it occurs.

i) Fixed asset investments

Investments are stated at market value. It is the Society’s policy to keep valuations up to date such that when investments are sold there is no gain or loss arising to previous years. As a result the SOFA includes those unrealised gains and losses arising from the revaluation of the investment portfolio throughout the year.

Fixed asset investments will include cash held by the investment managers which is intended for investment or held as part of the portfolio.

MS Society

48

Year ended 31 December 2024

Notes to Consolidated Accounts (continued)

2. Accounting policies (continued)

j) Investments included within current assets

Investments included within current assets are monies held in deposit accounts or in short-term notice accounts (less than 3 months).

l) Cash at bank and in hand

Cash at bank and in hand refers to monies held in current accounts, bank accounts within the Society's cash pooling scheme and cash.

m) Financial instruments

Recognition criteria for financial instruments appears below:

Financial instrument
Measurement criteria (initial and subsequent)
Financial instrument
Measurement criteria (initial and subsequent)
Cash
Debtors including trade debtors and loans receivable
Creditors
Bank deposits
Investments
Cash held, then on amortised cost
Settlement amount or amount advanced then at amortised cost
Settlement amount after trade discounts then at amortised cost
Cash amount of deposit then at amortised cost
Transaction cost then at fair value (market value of quoted
investments)

n) Leasing

All operating leases and rental expenses are charged to the SOFA as incurred.

o) Pension costs

The Society has an ongoing defined contribution scheme with all amounts charged to the SOFA in respect to pension costs being the contribution payable in the year.

3. Critical accounting judgements and sources of estimation uncertainty

In the application of the charity’s accounting policies, which are described in note 2, Trustees are required to make judgements, estimates and assumptions about the carrying values of assets and liabilities that are not readily apparent from other sources. The estimates and underlying assumptions are based on historical experience and other factors that are considered to be relevant. Actual results may differ from these estimates.

The estimates and underlying assumptions are reviewed on an ongoing basis. Revisions to accounting estimates are recognised in the period in which the estimate is revised if the revision affects only that period, or in the period of the revision and future periods if the revision affects the current and future periods.

Below are two areas which represent the most signficant areas where judgement calls are required along with estimation uncertainty.

(i) Legacy accruals

Significant accounting judgements are made in establishing whether the charity has entitlement to legacies and in making reasonable estimates of the amounts to be received. In the case of properties, we will not accrue until the sale of the property has been completed because of uncertainty over the amount to be received.

(ii) Grants income

Income is accrued for multi-year grants when the grants are awarded unless there are substantive performance conditions that are reviewed each year. Sometimes this requires a judgement call on what is or is not a substantive condition.

MS Society

49

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

4. Role of volunteers

We have approximately 2,700 committed and active volunteers, many of whom have a personal connection to MS. Volunteers contribute throughout the Society by being Trustees, National Council members, fundraising, campaigning, signposting, being part of our Research Network, volunteering to support individuals affected by MS, and organising services through our volunteer-run groups. We have a large volunteer-run group network who raise and spend money locally to support those affected by MS in their area.

5. Analysis of income

Donations:
Direct marketing
Community and events
Partnership fundraising
Raised locally
Legacies
Charitable activities
Charges made by the volunteer-run group network to people affected by MS
Statutory sources
Other fees and grants
Other trading activities
MSS (Trading) Limited
Raffles, lotteries and similar
Sale of donated goods
Large fundraising events organised by national offices
Other (local fundraising events organised by volunteer-run groups and rent received)
Investment income
Dividend income receivable
Interest receivable
Other income (relates to the profit on the sale of fixed assets)
Total income
6. Expenditure
Raising funds
1. Living well with MS
2. Connected communities, powerful voices
3. Effective treatments and preventing MS
Direct Costs
2023
Support Costs
Apportioned
2024
£'000
591
539
1,531
1,351
1,762
1,673
2024
2023
£'000
£'000
Restated
Restated
£'000
27,012
24,763
5,762
5,651
2,058
1,908
6,621
5,958
6,501
5,665
8,175
6,258
7,348
5,249
Donations:
Direct marketing
Community and events
Partnership fundraising
Raised locally
Legacies
Charitable activities
Charges made by the volunteer-run group network to people affected by MS
Statutory sources
Other fees and grants
Other trading activities
MSS (Trading) Limited
Raffles, lotteries and similar
Sale of donated goods
Large fundraising events organised by national offices
Other (local fundraising events organised by volunteer-run groups and rent received)
Investment income
Dividend income receivable
Interest receivable
Other income (relates to the profit on the sale of fixed assets)
Total income
6. Expenditure
Raising funds
1. Living well with MS
2. Connected communities, powerful voices
3. Effective treatments and preventing MS
Direct Costs
2023
Support Costs
Apportioned
2024
£'000
591
539
1,531
1,351
1,762
1,673
2024
2023
£'000
£'000
Restated
Restated
£'000
27,012
24,763
5,762
5,651
2,058
1,908
6,621
5,958
6,501
5,665
8,175
6,258
7,348
5,249
Donations:
Direct marketing
Community and events
Partnership fundraising
Raised locally
Legacies
Charitable activities
Charges made by the volunteer-run group network to people affected by MS
Statutory sources
Other fees and grants
Other trading activities
MSS (Trading) Limited
Raffles, lotteries and similar
Sale of donated goods
Large fundraising events organised by national offices
Other (local fundraising events organised by volunteer-run groups and rent received)
Investment income
Dividend income receivable
Interest receivable
Other income (relates to the profit on the sale of fixed assets)
Total income
6. Expenditure
Raising funds
1. Living well with MS
2. Connected communities, powerful voices
3. Effective treatments and preventing MS
Direct Costs
2023
Support Costs
Apportioned
2024
£'000
591
539
1,531
1,351
1,762
1,673
2024
2023
£'000
£'000
Restated
Restated
£'000
27,012
24,763
5,762
5,651
2,058
1,908
6,621
5,958
6,501
5,665
8,175
6,258
7,348
5,249
Donations:
Direct marketing
Community and events
Partnership fundraising
Raised locally
Legacies
Charitable activities
Charges made by the volunteer-run group network to people affected by MS
Statutory sources
Other fees and grants
Other trading activities
MSS (Trading) Limited
Raffles, lotteries and similar
Sale of donated goods
Large fundraising events organised by national offices
Other (local fundraising events organised by volunteer-run groups and rent received)
Investment income
Dividend income receivable
Interest receivable
Other income (relates to the profit on the sale of fixed assets)
Total income
6. Expenditure
Raising funds
1. Living well with MS
2. Connected communities, powerful voices
3. Effective treatments and preventing MS
Direct Costs
2023
Support Costs
Apportioned
2024
£'000
591
539
1,531
1,351
1,762
1,673
2024
2023
£'000
£'000
Restated
Restated
£'000
27,012
24,763
5,762
5,651
2,058
1,908
6,621
5,958
6,501
5,665
8,175
6,258
7,348
5,249
Donations:
Direct marketing
Community and events
Partnership fundraising
Raised locally
Legacies
Charitable activities
Charges made by the volunteer-run group network to people affected by MS
Statutory sources
Other fees and grants
Other trading activities
MSS (Trading) Limited
Raffles, lotteries and similar
Sale of donated goods
Large fundraising events organised by national offices
Other (local fundraising events organised by volunteer-run groups and rent received)
Investment income
Dividend income receivable
Interest receivable
Other income (relates to the profit on the sale of fixed assets)
Total income
6. Expenditure
Raising funds
1. Living well with MS
2. Connected communities, powerful voices
3. Effective treatments and preventing MS
Direct Costs
2023
Support Costs
Apportioned
2024
£'000
591
539
1,531
1,351
1,762
1,673
2024
2023
£'000
£'000
Restated
Restated
£'000
27,012
24,763
5,762
5,651
2,058
1,908
6,621
5,958
6,501
5,665
8,175
6,258
7,348
5,249
4,014
1,899
1,013
2024
£'000
4,702
3,589
2,591
1,139
4,388
2023
£'000
11,628 11,707
14,075 13,101
107
653
292
242
98
545
1,052 885
65
489
427
660
170
54
471
397
425
188
1,811 1,535
2024
£'000
201
212
113
297
2023
£'000
413 410
797 14
29,776 27,652
Direct Costs
2023
2024
£'000
Restated
£'000
6,621
5,958
6,501
5,665
8,175
6,258
7,348
5,249
Support Costs
Apportioned
591
539
1,531
1,351
1,762
1,673
2024
2023
£'000
£'000
Restated
2,058
1,908
2023
2024
Total
8,032
£'000
£'000
6,849
Restated
10,233
5,788
7,338
9,256
7,972
7,720
27,012 24,763 5,762 5,651 32,774 30,414

Direct costs include grant expenditure to individuals and institutions - see note 7 for a breakdown of grants. Figures for 2023 have been restated see note 11 for further details

MS Society

50

Year ended 31 December 2024

Notes to Consolidated Accounts (continued)

6. Expenditure (continued)

Analysis of support costs apportioned

Total
Raising funds
1. Living well with MS
3. Effective treatments and
preventing MS
2. Connected communities,
powerful voices
2024
2023
£'000
£'000
151
153
86
97
94
100
70
68
Governance2
2024
2023
£'000
£'000
158
168
90
107
98
110
73
75
Management2
2024
2023
£'000
£'000
467
368
325
328
450
367
97
73
HR Costs1
2024
2023
£'000
£'000
334
339
191
215
208
221
155
150
Finance2
2024
2023
£'000
£'000
532
527
370
470
512
524
110
104
IT Support1
2024
2023
£'000
£'000
416
353
289
314
400
351
86
69
Facilities1
2024
2023
£'000
£'000
2,0581,908
1,3511,531
1,7621,673
591
539
Total
401
418
419
460
1,3391,136 888
925
1,5241,625 1,1911,087 5,7625,651

2023 costs are restated - see note 11 for further details.

Method of apportionment

1 Apportioned on the number of full-time staff equivalents.

2Apportioned based on total direct costs. Does not include management and finance costs that could be directly allocated to direct costs.

direct costs. direct costs.
Analysis of governance costs 2024
£'000
2023
£'000
Fees payable to the Charity's auditors for the audit of the annual accounts
Internal audit
Trustee expenses (Note 8)
Board support related costs
Total governance costs
46
149
5
201
44
141
3
230
401 418
7. Grants
Institutional grants: Research
Grants released
2024
2023
Total grant
Strategic Restated award
goals £'000 £'000 £'000
University College London (UCL)
3
Prof J Chataway, Efficient clinical trials programme
1,915 1,877 13,003
3
Dr D Chard, Predicting progressive MS: a longitudinal clinical and MRI stu
dy
110
- 166
3
Other grants awarded and write backs
118 105
2,143 1,982
University of Cambridge
3
Prof RJM Franklin, Cambridge Centre for Myelin Repair Renewal
355 451 1,850
3
Prof A Coles, A phase Iia trial of the ability of the combination of
metformin and clemastine to promote remyelination in people with
149 94 808
3
Other grants awarded and write backs
219 75
723 620
Swansea University
1 & 3
Dr. R Middleton, UK MS Register grant
390 366 2,000
3
Other grants awarded and write backs
73 -
463 366
University of Edinburgh
3
Prof A Williams, The Edinburgh MS Centre for Translational Research
371 365 1,847
Other grants awarded and write backs 28 (7)
399 358
Imperial College London
3
Prof R Nicholas, The MS and PD Tissue Bank
276 - 1,524
Other grants awarded and write backs 90 306
366 306
Balance carried forward 4,094 3,632

MS Society

51

Year ended 31 December 2024

Notes to Consolidated Accounts (continued)

7. Grants (continued) Grants released Grants released Total
grant
Strategic
Institutional grants: Research
2024 2023 award
Restated
goals £'000 £'000 £'000
Balance brought forward 4,094 3,632
Brunel University London
1
Dr D Bailey, iStep-MS II: a physical activity and sedentary behaviour intervention
for reducing fatigue in people living with MS
279 - 541
Queen's University, Belfast
3
Prof D Fitzgerald, Building capacity for a Multiple Sclerosis Centre of Excellence in
Northern Ireland
242
- 242
3
Other grants awarded
- 230
242 230
International Progressive MS Alliance
1 & 3
Grant to the alliance
240 247 240
University of Nottingham
3
Dr C Gilmartin, Early detection of progression in MS using OPM-MEG
139 - 139
1 & 3
Write backs and other grants awarded
41 185
180 185
Queen Mary, University of London
1 & 3
Grants awarded and write backs
143 102
143 102
Nottingham University Hospitals Trust
3
Dr R Abdel-Fahim, GUIDE-MS: lonGitudinal evolUtion of Iron rim and expanDing
lEsions in MS using ultra high field imaging at 7Tesla
111 - 226
Other grants awarded and write backs
University of Birmingham
University of Oxford
Kings College London
Northumbria University
Leeds Teaching Hospitals NHS Trust
Cambridge University Hospitals
University of Liverpool
Cardiff University
University of Southampton
University of Portsmouth
University of Plymouth
University of Bristol
Versus Arthritus
University of Glasgow
University of Sheffield
86
73
72
68
57
50
49
48
40
39
2
1
(1)
(2)
(7)
-
(96)
186
-
-
-
-
96
(9)
-
(38)
-
-
136
-
Glasgow Caledonian University
University of Salford
-
-
116
86
Liverpool John Moores University
Wellcome Trust - Medical Research Council Stem Cell Insitute, Univ of Cambridge
-
-
50
1
University of Exeter
University of Leeds
Leeds General infimary
-
-
-
(5)
(12)
(13)
575 498
Total institutional grants released for research
In-house research team and associated support costs
Research grants plus research team and associated support costs
5,864
1,084
4,894
1,070
6,948 5,964

MS Society

52

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

7. Grants (continued) 7. Grants (continued) 7. Grants (continued) Grants released Grants released
2024 2023
Other grants £'000 £'000
Individual support grants awarded
Other grants awarded
Total other grants
303
79
276
-
382 276
*Individual support grants are primarily awarded by volunteer-run groups.
Grant expenditure by goal (excluding support
costs) and creditor
2024
2023
Other grants
2024
2023
Research grants
Total
2024
Total
2023
Restated Restated
Creditor brought forward
Grants awarded by goal:
£'000
-
£'000
-
£'000
11,213
£'000
9,966
£'000
11,213
£'000
9,966
Goal 1 - Living well with MS
Goal 2 - Connected communities, powerful voices
382
4
276
-
836
-
723
-
1,218
4
999
-
Goal 3 - Effective treatments and preventing MS - - 5,028 4,171 5,028 4,171
386 276 5,864 4,894 6,250 5,170
Payments made (307) (276) (4,191) (3,647) (4,498) (3,923)
Creditor carried forward 79 - 12,886 11,213 12,965 11,213

2023 figures have been restated - see note 11 for further details.

8. Staff and Trustees costs

Total staff emoluments for the year were as follows: 2024
£'000
2023
£'000
Salaries (see note below)
National insurance
Pension
Redundancy payments
11,892
1,266
1,279
5
11,666
1,240
1,082
20
There was ex-gratia payments of £30k (2023: £Nil) 14,442 14,008
The average number of individuals employed by the Society during the year was as follows: Average head count
2024
Number
2023
Number
Charitable activities 223 228
Generating funds
Governance
71
2
66
2
296 296
Number of employees whose employee benefits (exc. employer 2024 2023

pension contributions) were over £60,000 in the year:
Number Number
£60,001-£70,000
£70,001-£80,000
£80,001-£90,000
£90,001-£100,000
£140,001-£150,000
£150,001-£160,000
14
4
1
2
-
1
12
2
-
3
-
1

All of the employees whose employee benefits were greater than £60,000 are members of a defined contribution pension scheme and the Society paid contributions of £196k (2023: £135k) for these employees.

MS Society

53

Year ended 31 December 2024

Notes to Consolidated Accounts (continued)

8. Staff and Trustees costs (continued)

Employee benefits paid to key management personnel

Key management personnel consist of the Trustees plus executive directors. The total amount of employee benefits to 6 (2023: 6) key management personnel in 2024 amounted to £676k (2023: £647k).

Trustees recognise the need to attract the breadth and depth of expertise required to achieve ambitious goals in a competitive employment market which includes commercial, public sector and charitable organisations. All vacancies are filled following an external recruitment process and if that process is initially unsuccessful a market supplement may be added to the remuneration package.

Total employee benefits for the Chief Executive in 2024 amounted to £191k (2023: £185k).

Trustee expenses and donations

The Trustees all give freely their time and expertise without any form of remuneration or other benefit in cash or kind (2023: £nil). Expenses paid to the Trustees in the year totalled £5k (2023: £3k). These expenses were made up of 8 Trustees (2023: 6 Trustees) reimbursed for their travel expenses £2k (2023: £2k) and accomodation expenses of £3k (2023: £1k).

9. Taxation

The Society has charitable status and is thus exempt from taxation of its income and gains falling within Chapter 3 Part 11 of the Corporation Tax Act 2010 or Section 256 of the Taxation of Chargeable Gains Act 1992 to the extent that they are applied to its charitable objectives. No material tax charges have arisen in its subsidiaries and no provision is required for deferred taxation.

Irrecoverable VAT has been charged against the relevant expenditure.

10. Net movements in funds
2024
£'000
Net movement in funds is arrived at after charging:
Depreciation of intangible and tangible fixed assets
395
Profit on disposal of fixed assets
797
2023
£'000
351
14
Fees payable to the Charity's auditors for the audit of the Charity's annual accounts
46
44
Fees payable to the Charity's auditors for other services to the group:
- The audit of the charity's subsidiary pursuant to legislation
4
5
- Other non audit services
2
2
11. Prior Year adjustment

An error occurred in the preparation of the 2023 annual report and account which resulted in expenditure being misallocated between restricted and unrestricted expenditure.

The incorrect values for research costs in the notes also affected the allocation of support costs across our goals and the amount of the designated fund transfer.

amount of the designated fund transfer.
Balance brought forward
Transfers
Expenditure incorrectly allocated as restricted
expenditure
Consolidated
Affect on fund balances on the prior year
adjustment
Designated
for Fixed
Assets
£'000
2,213
-
-


Designated
for research
£'000
13,499
-
(251)

General
funds
£'000
8,423
(656)
-

Total
Unrestricted
£'000
24,135
(656)
(251)

Total
Restricted
£'000
(8,347)*
656
251
Balance brought forward restated 2,213 13,248 7,767 23,228 (7,440)

MS Society

54

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

11. Prior Year adjustment (continued)
Balance brought forward
Transfers
Charity
Affect on fund balances on the prior year
adjustment
Expenditure incorrectly allocated as restricted
expenditure
Designated
for Fixed
Assets
£'000
2,213
-
-


Designated
for research
£'000
13,499
-
(251)

General
funds
£'000
8,406
(656)
-

Total
Unrestricted
£'000
24,118
(656)
(251)

Total
Restricted
£'000
(8,347)*
656
251
Balance brought forward restated 2,213 13,248 7,750 23,211 (7,440)
Statement of Financial Activities
Changes to allocation of expenditure

Living well with MS
Effective Treatments
Previous stated
Incorrect allocation of Research
grants
Costs apportioned based on the
goal split of research grants
Restated costs
Unrestricted
5,659
-
154
Restricted

3,012

(793)

-
Total

8,671
(793)

154
Unrestricted
123
-
502
Restricted
5,026

137

-
Total

5,149

137

502
5,813
2,219

8,032
625
5,163

5,788
Note 6 expenditure
Changes to allocation of expenditure

Living well with MS
Effective Treatments
Previous stated
Incorrect allocation of Research
grants
Restated costs
Direct Costs
7,087
(586)
Support costs
1,584
(53)
Total
8,671
(639)
Direct Costs
4,663
586
Support costs
486
53
Total
5,149
639
6,501 1,531 8,032 5,249 539 5,788
Movement in support cost Living well with MS Effective Treatments
Governance
Management
HR Costs
Finance
IT Support
Facilities
allocation as a result of
adjustment
Previously
stated
104
115
335
231
479
320

Adjustment
(7)
(8)
(7)
(16)
(9)
(6)
Restated
costs
97
107
328
215
470
314

Previously
stated
61
67
66
134
95
63

Adjustment
7
8
7
16
9
6
Restated
costs
68
75
73
150
104
69
1,584 (53) 1,531 486 53 539
Corrections to Note 7 Research grants
Name of institution
Grants affected
Goal
allocation


Previously
stated


Restated
University College London (UCL)
Other grants awarded and write backs
3
University of Cambridge
3
Cambridge Centre for Myelin Repair
previously stated £444k, now £451k. Rest
of change due to other grants & write backs
1,985
721
1,982
620
Swansea University
UK MS Register grant
1 & 3
- 366
University of Edinburgh
No change
3
Imperial College London
Other grants awarded and write backs
1 & 3
Queen's University, Belfast
Other grants awarded
3
Int. Progressive MS Alliance
No change
1 & 3
358
15
296
247
358
306
230
247
University of Nottingham
Write backs and other grants awarded
1 & 3
348 185
Queen Mary, University of London
No change
3
University of Oxford
No change
3
Totals carried forward
102
(96)
102
(96)
3,976 4,300
Corrections to Note 7 Research grants Corrections to Note 7 Research grants
Goal Previously
Name of institution Grants affected allocation stated
Restated
University College London (UCL) Other grants awarded and write backs 3 1,985 1,982
Cambridge Centre for Myelin Repair
University of Cambridge previously stated £444k, now £451k. Rest 3 721 620
of change due to other grants & write backs
Swansea University UK MS Register grant 1 & 3 - 366
University of Edinburgh No change 3 358 358
Imperial College London Other grants awarded and write backs 1 & 3 15 306
Queen's University, Belfast Other grants awarded 3 296 230
Int. Progressive MS Alliance No change 1 & 3 247 247
University of Nottingham Write backs and other grants awarded 1 & 3 348 185
Queen Mary, University of London No change 3 102 102
University of Oxford No change 3 (96) (96)
Totals carried forward 3,976 4,300

MS Society

55

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

11. Prior Year adjustment (continued)

Corrections to Note 7 Research grants

Corrections to Note 7 Research grants
Name of institution
Grants affected
Goal
allocation


Previously
stated


Restated
Balance brought forward
Kings College London
Other grants awarded and write backs
1
Cardiff University
Other grants awarded and write backs
3
University of Southampton
Other grants awarded and write backs
1
University of Plymouth
Other grants awarded and write backs
3
University of Glasgow
Other grants awarded and write backs
3
3,976
429
293
-
76
130
4,300
186
96
(9)
(38)
136
Glasgow Caledonian University
Other grants awarded and write backs
1
University of Salford
Other grants awarded and write backs
1
430 116
166 86
Liverpool John Moores University
No change
1
Wellcome Trust - MRC Stem Cell
Institute, Univ of Cambridge
No change
3
50
1
50
1
University of Exeter
No change
1
University of Leeds
No change
1
Leeds General infimary
No change
1
Rounding
Total research grants awarded
Changes to goal allocation 2023
Total research grants awarded as previously stated
Adjustmentsmade
Total research grants awarded restated
(5)
(12)
(13)
(1)
(5)
(12)
(13)
-
5,520 4,894
Living well
with MS
1,396
(673)

Effective
Treatments
4,124
47
723 4,171

Payments for research grants was previously shown as £4,273k and has been restated as £3,647k.

12. Related party transactions

12. Related party transactions
Transactions with MSS (Trading) Limited-subsidiary:
Balance brought forward - owed by MSS (Trading) Limited to the charity
2024
£
68,960
2023
£
172,406
Prior year Gift Aided profits remitted to the charity
Monies relating to MSS (Trading) Limited received/paid by the charity (net)
Monies relating to the charity received/paid by MSS (Trading) Limited (net)
(16,578)
-
9,491
(56,867)
(115,539)
37,882
Use of logo charge and management fee charged by the charity to MSS (Trading) Limited
Current year profits of MSS (Trading) Limited
Amount owing from MSS (Trading) Limited to the charity
14,500
36,335
14,500
16,578
112,708 68,960

Vicky Annis (Director of Corporate Services) is the treasurer of the MS International Federation (MSIF) and Nick Moberly (Chief Executive) is a trustee. In 2024 £208k (2023: £94k) of costs relating to the annual subscription fee and The May 50k were paid to MSIF.

13. Intangible Fixed Assets

13. Intangible Fixed Assets
Consolidated and Charity
Cost
Balance at 1 January
2024
£'000
1,649
2023
£'000
983
Additions
Disposals
Balance at 31 December
Accumulated depreciation
Balance at 1 January
Charge for year
Disposals
1,024
-
733
(67)
2,673 1,649
835
88
-
799
103
(67)
Balance at 31 December
Net book value at 31 December
923 835
1,750 814

Intangible assets relate to computer software and website costs.

MS Society

56

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

14. Tangible Fixed Assets

14. Tangible Fixed Assets
Consolidated and Charity
Cost
Balance at 1 January
Additions
Disposals
Balance at 31 December
Balance at 1 January
Charge for year
Disposals
Balance at 31 December
Net book value at 31 December 2023
Net book value at 31 December 2022
2024
£'000
1,082
-
-
Freehold,
Land and
Buildings
2024
£'000
1,249
-
(616)
Leasehold
Property
2024
£'000
8
4
(8)
Computers
2024
£'000
1,721
77
(361)
Fixtures
2024
£'000
1,389
-
(340)
Motor
Vehicles
2024
£'000
5,449
81
(1,325)
Total
1,082 633 4 1,437 1,049 4,205
529
28
-
759
84
(324)
8
1
(8)
1,221
194
(361)
1,389
-
(340)
3,906
307
(1,033)
557 519 1 1,054 1,049 3,180
525 114 3 383 - 1,025
553 490 - 500 - 1,543

15. Capital commitments

There were no capital commitments as at 31 December 2024 or 31 December 2023.

16. Investments

16. Investments
Consolidated and Charity
Market value at 1 January
2024
£'000
14,620
2023
£'000
15,665
Acquisitions at cost 251 3,246
Disposals at market value (3,268) (4,972)
Gains on investment assets
Market value at 31 December excluding movement in cash held
798 680
12,401 14,619
Movement in cash held 287 1
Market value of investments at 31 December 12,688 14,620

In addition to the above the charity balance sheet includes an investment of £2 in MSS (Trading) Ltd (Note 25).

Represented by
Assets held at market value
2024
£'000
2023
£'000
Investments listed on a Stock Exchange
Cash held as part of portfolio
10,653
2,035
12,872
1,748
12,688 14,620

Included within 'Investments listed on a Stock Exchange' are investment assets outside the UK of £5.7m (2023: £6.8m). All other investments are investment assets in the UK.

17. Debtors Consolidated Consolidated Charity Charity
2024
£'000
2023
£'000
2024
£'000
2023
£'000
Legacy income accrued (see note 18)
Trade debtors
Tax and VAT
Prepayments and accrued income
Amounts due from group companies
Other debtors
8,905
134
1,226
1,744
-
11
9,056
95
1,093
1,818
-
20
8,905
118
1,226
1,717
76
11
9,056
74
1,093
1,789
52
20
12,020 12,082 12,053 12,084

MS Society

57

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

18. Contingent Assets

Not included in the legacy income accrual (see note 17) are approximately £6.0m (2023: £5.4m) of legacies where we had received notification of a legacy but where measurement and/or entitlement was not confirmed at year end.

19. Creditors: amounts falling due within one year

Consolidated Consolidated Charity Charity
2024
£'000
2023
£'000
2024
£'000
2023
£'000
Research grants1
Trade creditors
Accruals and deferred income
Tax and Social Security
Other creditors
12,886
979
1,159
366
3
11,213
795
1,562
444
19
12,886
979
1,150
366
3
11,213
795
1,547
444
19
15,393 14,033 15,384 14,018

1 The majority of research grants are released a year at a time and, in theory, the full amount of the creditor will be due for payment within 1 year. Movement in grant creditors is now included in note 7 grants.

In addition to the amounts committed and accrued noted above, there are also authorised research grants which are subject to an annual review. The total amount authorised but not accrued as expenditure at the year end was £12.9m (2023: £14.3m). This amount will be funded by future income and the designated fund set up for the appeal

20. Provisions for liabilities

20. Provisions for liabilities
Consolidated Charity
2024
£'000
2023
£'000
2024
£'000
2023
£'000
Provisions 94 62 94 62
21. Deferred income
2024
£'000
2023
£'000
Balance brought forward 257 257
Balance carried forward 257 257

Deferred income is made up of two components:

Accruals and deferred income includes deferred income of £257k (2023: £257k) relating to legacy monies in respect to a life interest. The Society does not have entitlement to these funds until the death of the life interest at which point these monies will be recognised as income. Also, until that point, any interest arising from these funds is passed to the life interest.

22. Statement of funds

22. Statement of funds
Consolidated and charity funds At
1/1/2024
Income Expenditure Transfers Other gains
and losses
At
31/12/2024
Restated
General Funds
Designated Funds
£'000
7,767
£'000
22,920
£'000
(19,917)
£'000
(5,422)
£'000
776
£'000
6,124
Net book value of intangible and tangible fixed
assets held
2,213 - (399) 822 - 2,636
Research funds1 13,248 - (1,656) 1,750 - 13,342
Total Designated Funds
Total Unrestricted Funds
15,461 - (2,055) 2,572 - 15,978
23,228 22,920 (21,972) (2,850) 776 22,102

MS Society

58

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

22. Statement of funds (continued)

22. Statement of funds (continued)
At
Consolidated and charity funds
1/1/2024
**Income ** Expenditure Transfers Other gains
and losses
At
31/12/2024
Restated
£'000 £'000 £'000 £'000 £'000 £'000
Restricted Funds for research1
Efficient clinical trialsprogramme
(4,112)
102 (2,307) 1,958 - (4,359)
Edinburgh MS Centre
(965)
58 (460) 500 - (867)
MS Tissue Bank
(354)
- (327) - - (681)
Simvasatinproject
(714)
4 (2) 126 - (586)
MS Register
(877)
15 (468) 862 - (468)
A phase 2a trial of the ability of the
combination of metformin and clemastine to
promote remyelination in people with
relapsingMS
(337)
- (177) 159 - (355)
Cambridge centre myelin repair renewal
(1,008)
88 (452) 1,019 - (353)
iStep-MS II: a physical activity and sedentary
behaviour intervention for reducing fatigue in
people livingwith MS
-
- (331) - - (331)
Building capacity for a MS Centre of
Excellence in Northern Ireland
-
- (286) - - (286)
International Progressive MS Alliance
(255)
(3) (284) 255 - (287)
Participatory Research into Minoritised
Patient Experiences of MS Care
(157)
- (159) 89 - (227)
The role of Nurr1 in the interplay of
inflammation and neurodegeneration in MS
(101)
- (111) - - (212)
Predicting progressive MS: A longitudinal
clinical and MRI study
(66)
- (130) - - (196)
Early detection of progression in MS using
OPM-MEG
-
- (165) - - (165)
Assessing NHS ImplemeNTation of an onlinE
Resilience-training Acceptance and
Commitment Therapy (ACT) programme to
preventjob loss in MS(INTER-ACT MS)
(81)
- (67) - - (148)
Determining the Effectiveness of Early
Intensive Versus Escalation approaches for
the treatment of Relapsing-remittingMS
(322)
- - 180 - (142)
Exercise/Physical Activity for Symptom and
Disease Management in people moderately
to severelyaffected with MS.
(142)
- - - - (142)
Digital Health Therapeutics for treating MS
symptoms
(140)
- - - - (140)
Co-design of a self-management education
programme for adults with MS experiencing
bowelproblems
(135)
- - - - (135)
GUIDE-MS: lonGitudinal evolUtion of Iron rim
and expanDing lEsions in MS using ultra high
field imagingat 7Tesla
-
- (131) - - (131)
Developing, optimising and implementing a
blended digital self-management tReatmEnt
for FatigUe in multiplE scLerosis (REFUEL-
MS)
(128)
- - - - (128)
Definingthe role KIF21B inglia
(123)
- - - - (123)
DELIVER-MS long-term extension
(117)
- - - - (117)
Understanding how Epstein Barr virus
promotes the development of MS
(61)
78 (130) - - (113)
#ChariotMS - Cladribine to halt deterioration
inpeople with advanced MS
(258)
- - 150 - (108)
Amount carried forward
(10,453)
342 (5,987) 5,298 - (10,800)

MS Society

59

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

22. Statement of funds (continued)

Consolidated and charity funds At
1/1/2024
**Income ** Expenditure Transfers Other gains
and losses
At
31/12/2024
Restated
£'000 £'000 £'000 £'000 £'000 £'000
Amount brought forward (10,453) 342 (5,987) 5,298 - (10,800)
Investigating the eye as a window to brain
inflammation in Multiple Sclerosis
(116) 14 (5) - - (107)
Regulation of T cells that helpB cells in MS - - (107) - - (107)
Greater Manchester MS Information
Network(GMMSIN)
(105) - - - - (105)
Other research funds (2,231) 5,470 (2,954) (2,448) (2,163)
Project Sage2 - 100 (100) - - -
Geographic restrictions3 3,413 710 (1,471) - - 2,652
Other sundry restricted funds
Total restricted income funds
1,760 220 (175) - - 1,805
(7,732) 6,856 (10,799) 2,850 - (8,825)
Endowment funds
Margaret Hutchinson memorial fund -
Borders area
Derby volunteer-run group endowment
282
10
-
-
(3)
-
-
-
21
-
300
10
Total endowment funds
292
-
Total funds
15,788
29,776
Notes on individual funds appear at the bottom of this note.
292 - (3) - 21 310
15,788 29,776 (32,774) - 797 13,587
2023 Funds statement - restated At Other gains At
Consolidated and charity funds
General Funds
Designated Funds
1/1/2023
£'000
10,241
Income
£'000
20,031
Expenditure
£'000
(19,427)
Transfers
£'000
(3,733)
£'000
655
and losses
31/12/2023
£'000
7,767
Net book value of intangible and tangible
fixed assets held
1,818 - (338) 733 - 2,213
Research funds1
Total Designated Funds
Total Unrestricted Funds
12,729 - (1,136) 1,655 - 13,248
14,547 - (1,474) 2,388 - 15,461
24,788 20,031 (20,901) (1,345) 655 23,228
Restricted Funds for research1
Efficient clinical trialsprogramme (2,795) 487 (2,454) 650 - (4,112)
Edinburgh MS Centre (711) 138 (492) 100 - (965)
MS Tissue Bank (335) - (354) 335 - (354)
Simvasatinproject (748) 51 (17) - - (714)
MS Register (441) 15 (451) - - (877)
A phase 2a trial of the ability of the
combination of metformin and clemastine to
promote remyelination in people with
relapsingMS
(503) - (114) 280 - (337)
Cambridge centre myelin repair renewal (706) 102 (584) 180 - (1,008)
Amount carried forward (6,239) 793 (4,466) 1,545 - (8,367)

MS Society

60

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

22. Statement of funds (continued)

PRIOR YEAR - Restated At Other gains At
Consolidated and charity funds 1/1/2023
£'000
Income
£'000
Expenditure
£'000
Transfers
£'000
£'000
and losses
31/12/2023
£'000
Amount brought forward (6,239) 793 (4,466) 1,545 - (8,367)
Building capacity for a MS Centre of
Excellence in Northern Ireland
- - - - - -
International Progressive MS Alliance (278) 36 (313) 300 - (255)
Participatory Research into Minoritised
Patient Experiences of MS Care
(157) - - - - (157)
The role of Nurr1 in the interplay of
inflammation and neurodegeneration in MS
(101) - - - - (101)
Predicting progressive MS: A longitudinal
clinical and MRI study
(66) - - - - (66)
Early detection of progression in MS using
OPM-MEG
- - - - - -
Assessing NHS ImplemeNTation of an
onlinE Resilience-training Acceptance and
Commitment Therapy (ACT) programme to
preventjob loss in MS(INTER-ACT MS)
(81) - - - - (81)
Determining the Effectiveness of Early
Intensive Versus Escalation approaches for
the treatment of Relapsing-remittingMS
(320) - (2) - - (322)
Exercise/Physical Activity for Symptom and
Disease Management in people moderately
to severelyaffected with MS.
- - (142) - - (142)
Digital Health Therapeutics for treating MS
symptoms
- - (140) - - (140)
Co-design of a self-management education
programme for adults with MS experiencing
bowelproblems
(48) - (86) - - (134)
GUIDE-MS: lonGitudinal evolUtion of Iron
rim and expanDing lEsions in MS using ultra
high field imagingat 7Tesla

-
- - - - -
Developing, optimising and implementing a
blended digital self-management tReatmEnt
for FatigUe in multiplE scLerosis (REFUEL-
MS)

(148)
- - 20 - (128)
Definingthe role KIF21B inglia - - (123) - - (123)
DELIVER-MS long-term extension - - (117) - - (117)
Understanding how Epstein Barr virus
promotes the development of MS
(94) 50 (17) - - (61)
#ChariotMS - Cladribine to halt deterioration
inpeople with advanced MS

(558)
- - 300 - (258)
Investigating the eye as a window to brain
inflammation in Multiple Sclerosis
- - (116) - - (116)
Regulation of T cells that helpB cells in MS - - - - - -
Greater Manchester MS Information
Network(GMMSIN)
- - (105) - - (105)
Other research funds (3,420) 4,028 (2,020) (820) - (2,232)
Project Sage2 - 350 (350) - - -
Geographic restrictions3 2,424 1,886 (882) - - 3,428
Other sundry restricted funds
Total restricted income funds
1,898 478 (631) - - 1,745
(7,188) 7,621 (9,510) 1,345 - (7,732)

MS Society

61

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

22. Statement of funds (continued)

PRIOR YEAR - Restated At Other gains At
Consolidated and charity funds
Endowment funds
Borders area
Derby volunteer-run group endowment
Total endowment funds
Total funds
1/1/2023
Income Expenditure
Transfers
31/12/2023
£'000
£'000
£'000
£'000
£'000
£'000
and losses
272
10
-
-
(3)
-
-
-
13
-
282
10
282 - (3) - 13 292
17,882 27,652 (30,414) - 668 15,788

Notes on note 22 Statement of funds

1 There is an appeal ('Stop MS Appeal') to raise over £100m for research over the next 10 years. £30m of this was earmarked to come from unrestricted income and is represented by the designated fund. £3m was transferred into the designated fund in 2024. Other transfers relate to generally restricted research funds being allocated against specific research grants.

2 Project Sage refers to a project to implement a new Customer Relationship Management (CRM) system.

3 Geographic restrictions arise where a donor has specifically asked that monies be used in a certain area and/or spent by a particular MSS group. In some cases these groups may have been given considerable discretion on the use of these funds including using the funds outside of their own locality in which they serve.

Note: The funds of the charity include £2 (2022: £2) relating to the total funds of MSS (Trading) Ltd.

Restatements to 2023 arising from the prior year adjustment (see note 11)

Restatements to 2023 arising from the prior year adjustment (see note 11) Restatements to 2023 arising from the prior year adjustment (see note 11) Restatements to 2023 arising from the prior year adjustment (see note 11)
Expenditure
Transfers
c/fwd
As Previously stated
Expenditure Transfers
c/fwd
As Restated
Efficient clinical trialsprogramme
(2,417)
650 (4,075) (2,454) 650 (4,112)
Edinburgh MS Centre
(485)
100 (958) (492) 100 (965)
MS Tissue Bank
-
- (335) (354) 335 (354)
Simvasatinproject
(17)
- (714) (17) - (714)
MS Register
(5)
- (431) (451) - (877)
A phase 2a trial of the ability of the
combination of metformin and clemastine to
promote remyelination in people with
relapsingMS
(112)
280 (335) (114) 280 (337)
Cambridge centre myelin repair renewal
(568)
180 (992) (584) 180 (1,008)
International Progressive MS Alliance
(309)
300 (251) (313) 300 (255)
Determining the Effectiveness of Early
Intensive Versus Escalation approaches for
the treatment of Relapsing-remittingMS
-
- (319) (2) - (322)
Exercise/Physical Activity for Symptom and
Disease Management in people moderately
to severelyaffected with MS.
(516)
- (516) (142) - (142)
Digital Health Therapeutics for treating MS
symptoms
(514)
- (514) (140) - (140)
Co-design of a self-management education
programme for adults with MS experiencing
bowelproblems
-
- (48) (86) - (134)
Developing, optimising and implementing a
blended digital self-management tReatmEnt
for FatigUe in multiplE scLerosis (REFUEL-
MS)
-
20 (128) - 20 (128)
Definingthe role KIF21B inglia
(114)
- (114) (123) - (123)
DELIVER-MS long-term extension
(351)
- (351) (117) - (117)
Investigating the eye as a window to brain
inflammation in Multiple Sclerosis
(109)
- (109) (116) - (116)
Greater Manchester MS Information
Network(GMMSIN)
(199)
- (199) (105) - (105)
Other restricted
(2,570)
(736) (2,699) (2,020) (820) (2,232)

MS Society

62

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

23. SOFA 2023

23. SOFA 2023 23. SOFA 2023 23. SOFA 2023
Income from: Unrestricted
funds
Restated
£'000
Restricted
funds
Restated
£'000
Total Funds
Restated
£'000
Donations 7,525 4,182 11,707
Legacies receivable
Charitable activities
Other trading activities
Investment income
Other income - Profit on sale of assets
10,656
310
1,125
401
14
2,445
575
410
9
-
13,101
885
1,535
410
14
Total income
Expenditure on:
Raising funds
Charitable activities
Goal 1 - Living well with MS
Goal 2 - Connected communities, powerful voices
Goal 3 - Effective treatments and preventing MS
20,031 7,621 27,652
7,370
5,813
7,093
625
1,886
2,219
245
5,163
9,256
8,032
7,338
5,788
Total expenditure
Net gains on investments
Net income / (expenditure) after investments
Transfers
20,901 9,513 30,414
667 13 680
(203)
(1,345)
(1,879)
1,345
(2,082)
-
Other recognised gains and losses:
Other recognised gains and losses: (12) - (12)
Net movement in funds (1,560) (534) (2,094)
24. Analysis of net assets between funds
Restricted & Endowment
Restricted & Endowment
Unrestricted funds funds
Total Total
Fund balances at 31 December are 2024 2023
Restated
2024 2023
Restated
2024 2023
Restated
represented by £'000 £'000 £'000 £'000 £'000 £'000
Intangible fixed assets 1,750 814 - - 1,750 814
Tangible fixed assets
Investments
Net current liabilities
886
12,362
7,104
1,399
14,322
6,693
139
326
(8,980)
144
298
(7,882)
1,025
12,688
(1,876)
1,543
14,620
(1,189)
22,102 23,228 (8,515) (7,440) 13,587 15,788
24. Analysis of net assets between funds 24. Analysis of net assets between funds
Restricted & Endowment
Unrestricted funds funds Total Total
2024 2023 2024 2023 2024 2023
Fund balances at 31 December are Restated Restated Restated
represented by £'000 £'000 £'000 £'000 £'000 £'000
Intangible fixed assets 1,750 814 - - 1,750 814
Tangible fixed assets 886 1,399 139 144 1,025 1,543
Investments 12,362 14,322 326 298 12,688 14,620
Net current liabilities 7,104 6,693 (8,980) (7,882) (1,876) (1,189)
22,102 23,228 (8,515) (7,440) 13,587 15,788

MS Society

63

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

25. MSS (Trading) Limited

The Society has a wholly owned trading subsidiary which is registered in England and Wales (company number 02895015). MSS (Trading) Limited raises funds via commercial activities and sponsorship. Any taxable profits made by MSS (Trading) Limited are donated to the Society under Gift Aid. A summary of the trading results which have been consolidated on a line by line basis are shown below.

MSS (Trading) Limited
Profit and loss account
Retail
Sales
Cost of sales
Gross profit
Administration
Net profit before taxation and Gift Aid
Taxation
Retained profit carried forward
Called up share capital
Authorised:
1,000 ordinary shares of £1 each
Allotted, called up and fully paid:
2 ordinary shares of £1 each
2024
£'000
65
2023
£'000
54
65
(9)
54
(17)
56
(20)
37
(21)
36
-
16
-
36 16
2024
£
1,000
2023
£
1,000
2 2

26. Share Capital

The Society has no issued share capital as it is a company limited by guarantee.

27. Pension funds

Defined contribution schemes

The MS Society contributes towards a number of defined contribution schemes. The cost of these schemes is charged to the SOFA and amounted to £1.28m (2023: £1082k). They did not give rise to any provisions/reserves. At the end of the year £86k (2023: £86k) was owed to the pension provider.

28. Operating leases

Operating lease payments due:
At 31 December the group and charity had total operating lease
commitments as follows:
Land and
Buildings
2024
£'000
Other
2024
£'000
Land and
Buildings
2023
£'000
Other
2023
£'000
within one year
within two to five years
over five years
394
292
14
11
-
-
374
581
42
21
10
-
700 11 997 31

Lease payments recognised as an expense were £395k (2023: £416k)

During 2024 the charity entered into a sale and leaseback of a property in Northern Ireland. The terms of this arrangement effectively meant the lease was prepaid - lease payments prepaid relating to within one year amounted to £27k, within two to five years to £108k and over five years £183k. The total prepaid amounting to £318k.

MS Society

64

Notes to Consolidated Accounts (continued)

Year ended 31 December 2024

29. Monies from the Medical and Healthcare industry

The Society has a policy position on working with the Medicines and Healthcare Products Industry which is available from the Society's website. Under this policy, the Society will report collaborations and financial contributions over £5,000 received from the Medicines and Healthcare industry.

the Medicines and Healthcare industry.
2024
Collaborations and financial contributions over £5,000 to the Society were:
£'000
2023
£'000
Roche Products Ltd
45
30
Merck Serono Ltd
20
20
Genzyme, a Sanofi Company
10
Theraposture Ltd
7
Bristol Myers Squibb (formerly Celgene)
-
-
13
7

30. International Progressive MS Alliance

The Society is part of the International Progressive MS Alliance which was set up in 2013 to fund grants into progressive MS. The International Progressive MS Alliance consists of MS charities around the world and other interested organisations such as foundations, trusts and corporate entities. The MS Society is a founding member and joined the Alliance as a managing member giving it influence on the research the Alliance will fund. There are five other MS charities who are managing members. These are the Associazione Italiana Sclerosi Multipla (Italy), MS Research Australia, Multiple Sclerosis International Federation, Multiple Sclerosis Society of Canada and National Multiple Sclerosis Society (USA).

In addition to managing members there are:

●13 other MS organisations who are members of the Alliance and they represent Belgium, Brazil, Denmark, Finland, France (2), Germany, Iceland, Ireland, Netherlands, Norway, Spain and Sweden.

●20 trusts and foundations members.

●5 pharmaceutical companies are industry forum members.

MS Society

65

Statement of Financial Activities (SOFA) - charity only

Statement of Financial Activities (SOFA) -charity only Statement of Financial Activities (SOFA) -charity only
Year ended 31 December 2024
Unrestricted
Note
funds
Income from:
5
£'000
Donations
7,891
Legacies receivable
12,348
Charitable activities
367
Other trading activities
1,081
Investment income
403
Other income
797
Restricted
funds
£'000
3,754
1,727
685
680
10
-
2024
Total
£'000
11,645
14,075
1,052
1,761
413
797
2023
Restated
Total
£'000
11,707
13,101
885
1,496
410
14
Total income
5
22,887 6,856 29,743 27,613
Expenditure on:
6
Raising funds
Raising funds 7,909 2,310 10,219 9,233
Charitable activities
Goal 1 - Living well with MS
Goal 2 - Building communities, powerful voices
Goal 3 - Effective treatments and preventing MS
5,659
7,523
867
2,313
197
5,982
7,972
7,720
6,849
8,032
7,338
5,788
Total expenditure
6
21,958 10,802 32,760 30,391
Net gains/(losses) on investments
15
Net income
777 21 798 680
1,706 (3,925) (2,219) (2,098)
Other recognised gains and losses:
Other recognised gains and losses (1) - (1) (12)
Net movement in funds 1,705 (3,925) (2,220) (2,110)

MS Society

66

Thank you

We want to thank all our donors for their generosity. This includes all trusts and corporations, those who wish to remain anonymous, our local groups and those who have left us a legacy. We would also like to thank our many celebrity supporters and friends for their work in raising both awareness and funds.

Special thanks for these donors and supporters:

Accenture UKIA Alliotts LLP Aparito The John M Archer Charitable Trust Ascot Underwriting Holdings Limited Penny Avis and Peter Catterall The Patricia Baines Trust Robert Barr Charitable Trust Michael Brady Limited Bill Brown 1989 Charitable Settlement The Betty Lawes Foundation The Philip Breeze Charity Brunswick Group The Buccleuch Charitable Foundation Richard Burns The Cairns Family Carers Trust Wales Chase Sinclair Clark and Vanessa and James Clark Tom Colraine Iain Conn and Caroline Shorten Conn Crown Agents Bank The Curry Family Trust The D'Almeida Charitable Trust Digitalis Homa & David Driver The Durant Family AC Farstad Michael and Deborah Fiddy FieldRose Charitable Trust Four Daughters Charitable Trust The Hugh Fraser Foundation Gartner UK Limited GeneSys Legacy Project Geoffrey and Pauline Martin Trust The G C Gibson Charitable Trust Lynne and Tom Gosling Sarah and Nigel Hammond The Charlotte Tana Heymann Charitable Trust Paul and Janet Hough Thomas Hunt

David and Wendy Hunter The Jones Family Charitable Trust Mr and Mrs Mark Joseph R S Macdonald Charitable Trust Charles and Nicky Manby Ian and Elizabeth Marchant The Meikle Foundation The Mercer Family Charitable Foundation Merck Healthcare MetLife UK The Northwood Charitable Trust Geoffrey Owen Peter Phillips The Peacock Charitable Trust The Pilkington Charities Fund The Sir James Reckitt Charity Roche Products Limited The M A H Roe Charitable Trust Belinda and Ferrill Roll Sanofi Scottish Government ShareGift – The Orr Mackintosh Foundation Stuart Secker David and Gabrielle Silver D & C Slade Sovereign Capital Partners Joseph and Lilian Sully Foundation Christine and Keith Swabey TA Associates (UK), LLP Mike & Catherine Thompson and Warburg Pincus LLC. Neil Urquhart Wales & West Utilities Marion and Michael Warshaw Sara Weller Garfield Weston Foundation Alex & Gareth Whiley The Wixamtree Trust Mark Wood Dr R Youldon

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Founder Sir Richard Cave* KCVO, CB, KCSG, DL

Vice-President John Walford* OBE

Chair Prof. Sir Paul Curran

Vice Chair Sarah Schol (to July 2024) Emily Revess (from July 2024)

Bankers Barclays Bank 1 Churchill Place, London E14 5HP

Auditors Haysmacintyre LLP 10 Queen Street Place, London EC4R 1AG

Solicitors Broadfield LLP (formerly BDB Pitmans) One Bartholomew Close, London, EC1A 7BL

Anderson Law LLP Manor House, Howbery Park, Benson Lane, Wallingford, Oxfordshire OX10 8BA

Investment Managers Rathbones Investment Management 8 Finsbury Circus, London EC2M 7AZ

Treasurer Nick Keveth

Key management personnel

Country Directors

Trustees Dr. Shewly Choudhury Prof. Sir Paul Curran Jason Jaspal (from 11 July 2024) Nick Keveth Leah Mates (from 11 July 2024) Bayan Mohajeri Chris Murray Emily Revess Sarah Schol (to 31 Dec 2024) Dr. Stephanie Wright (from Jan 2024) Stephen O’Keane (from Jan 2024) David Silver Polly Williams

Chief Executive Nick Moberly

Executive Directors Vicky Annis Executive Director of Corporate Services

Dr. Sarah Rawlings Executive Director of Research and External Affairs

Ed Tait Executive Director of Engagement and Income Generation

Gavin Atkins (from Feb 2024) Executive Director of Support and Services

Northern Ireland David Galloway (to Jan 2024) Stewart Finn (from Feb 2024)

Cymru / Wales Shelley Elgin

Scotland Morna Simpkins (to Aug 2024) Keith Parks (interim from Sept 2024)

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We’re the MS Society. Our community is here for you through the highs, lows and everything in between. We understand what life’s like with MS.

Together, we are strong enough to stop MS. mssociety.org.uk

Contact us MS National Centre 020 8438 0700 info@mssociety.org.uk MS Helpline Freephone 0808 800 8000 (weekdays 9am-9pm) helpline@mssociety.org.uk

Online mssociety.org.uk facebook.com/MSSociety twitter.com/mssocietyuk

MS Society Scotland 0131 335 4050 msscotland@mssociety.org.uk

MS Society Northern Ireland 028 9080 2802 nireception@mssociety.org.uk

MS Society Cymru mscymru@mssociety.org.uk

Multiple Sclerosis Society Registered charity nos. 1139257 / SCO41990 Registered as a limited company in England and Wales 07451571 Registered office: Carriage House, 8 City North Place, London, N4 3FU