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2025-03-31-accounts

Muscular Dystrophy Group of Great Britain and Northern Ireland

Annual Report 2024/25 Together we are stronger

Muscular Dystrophy UK Annual Report | 3

Contents

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||| |---|---| |A message from our| |Chair and Chief Executive|4| |Zoe and Archie’s story|6| |About us|7| |The year in numbers|8| |Looking back on what we achieved|9| |Our research advances|12| |Driving change for access| |to specialist care and support|16| |Living well|20| |Our work in Scotland|24| |The difference your support made|26| |RHS Chelsea Flower Show success|30| |Our President’s Award winners|33| |Our finances|34| |Our future plans|36| |Thank you|38| |Our policies|42| |Governance, structure| |and management|46| |Independent auditor’s report|48| |Financial statements and notes|52|

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P12
Our research
advances
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P20
Living
well
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P30
RHS Chelsea Flower
Show success
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Front cover and opposite photographer: Chris O’Donovan

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A message from our Chair and Chief Executive

Welcome to this year’s Annual Report. A year in which we’ve continued to increase the impact of our research, services and influencing work. In November, we were delighted to welcome Andy Fletcher as our new Chief Executive. Since then, Andy has been getting to know the charity and meeting our extraordinary community.

In 2024/25, we continued to fund groundbreaking research into a range of muscle wasting conditions. We were delighted to commit significant funding to the LifeArc Centre for Rare Mitochondrial Diseases, as well as to three projects focused on developing treatments for congenital muscular dystrophy, as part of our strategic partnership. And, following a new strategic grant round, a £1m award to Professor Mary Reilly at University College London to develop a new scanning method to spot small changes in CharcotMarie-Tooth disease (CMT).

As part of our regular grant round, we funded a further 12 projects with a lifetime funding commitment of £1.7m. This brought the number of our live research programmes to 45, focusing on 25 different conditions. These grants, alongside our strategic research investment, show our commitment to funding innovative programmes designed to better understand and treat muscle wasting conditions for the benefit of our community.

After research and clinical trials comes access to treatments, and this too has accelerated at pace since the first treatment for a muscle wasting condition became available in the UK in 2016. This year, we were delighted to have helped secure the approval of Vamorolone, a new treatment for Duchenne muscular dystrophy. We were also involved in a further eight NHS treatment appraisals that could potentially benefit our community.

As well as funding research to give hope for the future, we also continue to provide direct support to people with muscle wasting conditions so they can live their life fully today. This year we supported more than 3,300 people through our helpline, and provided equipment grants to 131 people living with a muscle wasting condition. Our peer-to-peer support network also continues to grow and thrive.

This year, we continued to support and influence the NHS and the development of neuromuscular services, and

speak up for our community. Our conferences for Allied Health Professionals and Care Advisers had more than 170 in-person attendees and our upskilling webinars continued to grow and attract professionals from across health and care services.

decade. This was launched in September 2025.

We finish this year once again proud of our wonderful community. Our research partners, support services and funders, volunteers, fundraisers, staff and trustees. Thank you for your support, your involvement, your stories, your requests and your continued passion to make our charity matter, because we all know how much our muscles matter.

We were delighted that our wonderful garden at the RHS Chelsea Flower Show exceeded all our expectations. The unique opportunity presented by Project Giving Back for a fully funded garden at the RHS Chelsea Flower Show 2024 culminated in winning Best in Show. The garden allowed us to reach people who had never heard of muscle wasting conditions, to give our community a voice, and to raise awareness of our work.

Thank you for your support.

Andy Fletcher

Chief Executive

While we live in uncertain times, we are committed to continuing to grow our impact to ensure that people living with muscle wasting conditions have the support they need. During the past year we have been developing a new, bold and ambitious strategy to lead our work over the next

Professor Michael Hanna

Chair

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Zoe and Archie’s story

Zoe’s son, Archie, was diagnosed with Duchenne muscular dystrophy in June 2024 at six years old. Our helpline team supported Zoe and her partner through the initial diagnosis with information about the condition, understanding what the genetics meant for their other son, Alfie, and providing counselling for Zoe.

“For years, I had a gut feeling something wasn’t right, but doctor after doctor dismissed my concerns. We were told Archie was just anaemic and would grow out of it. But he was always tiny, constantly ill, and exhausted — eventually needing a buggy for long walks. Even when we saw a paediatrician, we were brushed off. It was heartbreaking.

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Photographer: Chris O’Donovan
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“Everything changed when we were referred to Evelina London Children’s Hospital. For the first time, we felt listened to. A few weeks later, we received the devastating diagnosis: Archie had Duchenne muscular dystrophy.

“Evelina told us about Muscular Dystrophy UK, and reaching out to them was one of the best things I’ve done. Their helpline team was kind, compassionate, and gave me clear, reliable information. It’s so much to take in about what the future holds for our little boy. I didn’t know how to cope at all.

“The charity has supported our whole family. Archie’s grandma raised money at Christmas, and when she called to donate, they reminded her that they’re here for everyone. It meant so much for her to feel seen and supported too.

where they explained the science behind Duchenne. I had tried to Google the information, but speaking to someone allowed me to understand the facts so I could stop panicking unnecessarily. They gave me easy to understand leaflets too so that I could properly digest the information.

Muscular Dystrophy UK offered me one-to-one counselling sessions, which were a lifeline. Being able to speak openly and grieve in a safe space helped me begin to process what was happening.”

“We were also confused about the genetic side of Duchenne and whether our older son, Alfie, needed testing. We got back in touch with the helpline team, and I had a long phone call

“It’s still incredibly hard, but knowing we’re not alone, and that support is always there, has made all the difference.”

About us

We’re the leading charity for over 110,000 people in the UK living with one of over 60 muscle wasting and weakening conditions.

We connect people living with muscle wasting and weakening conditions, and all those around them: friends and family, healthcare professionals and scientists. So that everyone can get the healthcare, support and treatments needed to feel good, both mentally and physically.

We support people through every stage of their life, from the point of diagnosis to living the best life possible.

Objects of Muscular Dystrophy UK for the Public Benefit

Our mission

The Charity is established to promote awareness and care for those affected by muscular dystrophy and allied neuromuscular conditions.

We work to:

Our values

Public Benefit

The charity Trustees consider that they have complied with their duty in section 17 of the Charities Act 2011 to have due regard to Public Benefit guidance published by the Charity Commission and that the benefits that the charity provides are not unreasonably restricted.

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The year in numbers

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£1.7m £7.9m £2.15m
committed to raised committed
12 new research this year in strategic
projects research grants
Over
More than 260 £500,000
healthcare professionals raised at the 40th
attended our upskilling Anniversary Microscope Ball
webinars
Nearly More
80
Nearly
3,500 than 460
Trusts and
people supported people joined Foundations
through our our WhatsApp supported our
helpline communities work this year
Nearly 630,000 Over 1,750
visits to our website, up pieces of media coverage.
20% on the previous year A 18% increase in volume
of coverage year-on-year
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Looking back on what we achieved

This year’s achievements and performance measured against our 2024/25 objectives.

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Performance indicator Our achievements
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Performance indicator Our achievements
Award a grant as part of
our partnership with the
LifeArc Translational Rare
Disease Centre		 • Awarded a grant of £1.15m to
Professor Patrick Chinnery at
the University of Cambridge
Launch a new call
for £1m strategic
programmes grant		 • Awarded a grant of £1m to
Professor Mary Reilly at University
College London
Invest over £500,000 into
the 2024 new research
grants programme		 • Invested £640,000 into new
research grants, with a total
lifetime commitment of £1.7m
Continue to engage in
research partnerships,
including the MAGIC
consortium and the
LifeArc programmes		 • Announced new grants through
the LifeArc partnership programme
and contributed to communication
activities of the MAGIC consortium
Award grants as part of
three-year programme
to drive innovative
research into enhancing
the quality of life for
people living with muscle
wasting conditions		 • Awarded two new grants as part
of this scheme
Relaunch our partnership
with the Medical
Research Council to
support clinical
fellowships		 • This scheme is now live
Deliver at least £6m gross
fundraising budget		 • Delivered a gross budget of £7.9m
through active fundraising (£4.5m),
legacies (£2.6m) and other income
(£820k), which has resulted in a net
figure of £4.9m

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This year’s achievements and performance measured against our 2024/25 objectives - continued

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Performance indicator Our achievements
Invest in a new legacy proposition to maximise • Successfully launched our Change the Story legacy
the potential of this long-term income stream campaign in March 2025
Invest in a portfolio review of our events and • Using sector expertise and external market
campaigns to inform our strategic direction knowledge carried out a portfolio review resulting
from 2025/26 onwards in invaluable evidence-based insights
Deliver a successful garden at the RHS Chelsea • Delivered beyond expectations, culminating in
Flower Show 2024 winning Best in Show. This allowed us to reach new
audiences and raise awareness of our work
Provide accurate and accessible information, • Supported over 3,300 people through our helpline,
support and signposting, through our helpline a 23% increase on previous years
service and advocacy support
• Supported 130 advocacy cases
• Achieved the Patient Information Forum (PIF)
accreditation
Connect people living with muscle wasting • Held in-person Information Days/conferences in
conditions through our national events and England, North Wales and Scotland. Along with a
webinars, local groups, and our network of disability sports event, holistic physiotherapy events,
trained peer support volunteers and seven condition specific webinars.
Provide grants to members of our community • Provided 131 grants for essential mobility equipment
for essential powered mobility equipment
• Collaborated with SMA UK (SMArtMoves) and Whizz
Kidz to jointly fund grants for power wheelchairs
Deliver targeted campaigns on key areas of • Launched Missing People. Missing Support report
concern to our community and drive-up UK on unmet health and care needs in Scotland at
wide political awareness and support for the Scottish Parliament
muscle wasting conditions
• Advocated for improved financial security
throughout the year, highlighting the widespread
financial insecurity impacting on our community
Continue as co-chair of the Changing Places • Continued role as co-chair of the Changing Places
Consortium and complete UK Government Consortium until 31 March 2025, then formally
funded Changing Places programmes handed over to PAMIS as sole chair from April 2025
• Successfully concluded all government-funded
programmes under our management and
ensured full distribution of allocated funds
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This year’s achievements and performance measured against our 2024/25 objectives - continued

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Performance indicator Our achievements
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Performance indicator Our achievements
Provide unique national conferences and
virtual training opportunities for specialist
and non-specialist health professionals
involved in the care of people living with
muscle wasting conditions		 • Held upskilling webinars for 266 healthcare
professionals across different specialties
• Held neuromuscular conferences attended by
177 care advisors, clinical nurse specialists, and
allied health professionals
• Ran e-learning modules attended by
711 healthcare professionals
Provide regional networking, information
and intelligence sharing, and upskilling
opportunities to health professionals involved
in the care of people living with muscle
wasting and weakening conditions		 • Hosted eight regional neuromuscular
networks to support intelligence sharing and
strategic discussions on challenges faced by
different regions
Map the provision of specialist neuromuscular
services across the UK, seek to protect the
provision of specialist NHS neuromuscular
services, and secure additional NHS resource.
Recognise and disseminate best practice and
support neuromuscular services to navigate
ongoing healthcare commissioning and
delivery reforms		 • Published report highlighting best practice
and key challenges in neuromuscular services
evidenced by the findings of our Centre of
Excellence audit
Help to facilitate access to treatments for
muscle wasting and weakening conditions		 • Participated in eight treatment appraisals this year
Deliver £10m charitable expenditure budget
investing our reserves to cover the deficit		 • Spent total of £10.1m on work supporting
our community
Launch our new website providing a better
user experience and improved navigation		 • Launched our new website in May 2024
Launch a brand campaign to reach people
affected by the conditions who aren’t
currently engaging with the charity		 • Following insight and research we decided to
test and learn from a number of different activities
to further increase our reach including Meta ads,
engagement with healthcare professionals and
developing an online referral form

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Our research advances

High-quality research continues to play a key role in our work to improve the lives of people living with a muscle wasting condition. It helps us to better understand conditions and maximise treatment improvements.

Our research strategy Transforming lives through research remains the driving force for our research activity.

Our grant awards this year

This year, we committed £1.7m into 12 new research projects as part of our 2024 grant round. We’re proud to report that these new research projects cover a range of different conditions, including:

By funding innovative research, we’re accelerating progress in diagnosis, the monitoring of progression, and treatment development for muscle wasting conditions.

Our lay research panel helps us with the selection and approval process for this funding, and we would like to thank the members and our medical research committee for their time and expertise.

This year over 100 people contacted us through our research line.

Celebrating 20 years of the NorthStar programme

This year we celebrated 20 years of the NorthStar programme in which we’ve invested over £1.5m since 2004.

Over the past 20 years, the programme, led by Professor Francesco Muntoni and Dr Adnan Manzur, has transformed care and research for people living with Duchenne muscular dystrophy (DMD).

Today, it’s the world’s largest study tracking the progression of DMD over time. It currently involves over 2,000 boys and men across 23 centres in the UK. The findings of the programme have been instrumental in shaping clinical trial design, improving standards of care, and enhancing the quality of life for people living with DMD.

“ The NorthStar Network was established 20 years ago to help improve standards of care for boys with Duchenne muscular dystrophy across the entire country. Today, the improved standards have helped many boys living with the condition extend their lives into adulthood. ” Professor Francesco Muntoni

Spotting small changes in CMT to support greater accuracy in clinical trials

This year we committed £1m to University College London (UCL) for a project led by Mary Reilly, Professor of Clinical Neurology, to develop a new scanning method to spot small changes in Charcot-Marie-Tooth disease (CMT) and collect information from people living with CMT about how their condition affects their daily life.

This work will help make trials more accurate, showing more clearly if treatments are working, and will

Emily is a Muscular Dystrophy UK funded PhD student working on a project to explore whether controlling stress signals and taking nutritional supplements can help to treat non-reversible mitochondrial myopathies.

My interest in research began with my own health struggles. Knowing something’s going wrong inside your body, but being unable to control it is hard. I wanted to contribute to research that creates tangible outcomes that help individuals.”

Photographer: Chris O’Donovan

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three research grants this year with the aim of developing new treatments for congenital muscular dystrophy, a group of early-onset muscle weakening conditions with no effective treatments. This vital partnership was made possible thanks to an incredibly generous legacy gift and could bring us closer to potentially life-changing breakthroughs.

put the UK in a strong position to lead the way in finding effective treatments.

This funding also covers an initiative to get the UK ready for more CMT clinical trials. At present only one centre is set up to run clinical trials for CMT. With potential new treatments on the way, more centres are needed so a greater number of people can take part in trials closer to their homes.

“ This funding is pivotal. Success would break the longstanding therapeutic bottleneck in COL6-CMD and establish a modular delivery platform adaptable to other neuromuscular disorders where muscle fibroblast targeting is critical. ” Professor Haiyan Zhou, funding recipient

New centre to accelerate mitochondrial disease treatments

We awarded just over £1m to the LifeArc Centre to Treat Mitochondrial Disorders, led by Professor Patrick Chinnery, this year. The Centre brings together top clinicians, researchers, and the voices of people affected by mitochondrial diseases and works towards accelerating mitochondrial disease diagnosis and the development of much-needed treatments.

Research to support people living well with muscle wasting conditions

When we asked people living with muscle wasting conditions what research we should be focusing on, it was clear that quality of life was a priority.

A collaboration between the University of Cambridge, UCL, Newcastle University, The Lily Foundation, and sites in Birmingham, Manchester and Oxford, the centre is backed by a £7.5m grant from LifeArc.

In response, we launched a new funding programme to support this area. So far, we’ve backed two research projects aiming to ensure people with these conditions can live the best life possible.

Our investment will fund and train a new generation of scientists to lead future research into muscle wasting conditions.

Dr Christopher Morse is working with people affected by facioscapulohumeral muscular dystrophy (FSHD) and limb girdle muscular dystrophy (LGMD) to understand what helps, or gets in the way of, living well and how things can be improved. Dr Philip Hennis and his team are exploring methods that might help people with glycogen storage disease, like Pompe disease, exercise more safely.

Partnerships to drive forward new treatments for congenital muscular dystrophy

Working with partners helps our funding go further, allowing us to support more research and have a greater impact. Together with LifeArc we co-funded

When you live with a serious degenerative muscle wasting condition, having a good knowledge of the aspects that can improve your quality of life is important.”

John, living with Pompe disease

Highlights of our research funding

Research projects take time to deliver impact. Here are some key outcomes from grants we funded that came to an end in 2024/25.

Finding potential new treatments for CMT

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We funded research to look for new treatments for CMT, a condition where nerve signals struggle to reach the muscles, leading to weakness.

Dr Ivana Barbaric’s team at the University of Sheffield focused on mitochondria, the parts of cells that produce energy and are known to move poorly in CMT. By growing nerve cells in the lab, they developed a way to track how mitochondria move.

Speeding up diagnosis

Diagnosing muscle wasting conditions can take a long time. Professor Jordi Diaz-Manera from the University of Newcastle has developed a tool which, using body scans, can predict a diagnosis for 20 different conditions.

Using this method, they found several existing drugs that help improve movement in CMT nerve cells. These early results are promising, and the next step is to better understand how these drugs work and prepare them for further testing.

We’re now supporting the continuation of this research to increase the number of conditions the tool can predict. There is also a focus on improvements to make it more accurate, and easy for clinicians to use in appointments with patients.

Working towards a less invasive test for muscle wasting conditions

Diagnosing muscle wasting conditions often involves inserting a needle into the muscle to measure how signals from the brain are received and processed. This test can be painful and uncomfortable, especially for children.

We funded Dr Eduardo MartinezValdes at the University of Birmingham in developing a less invasive method that children preferred. Encouragingly, it collected almost the same information as a traditional needle test. With further development, it could support more accurate diagnosis and help track how these conditions change over time.

A new web application called Myo-Guide has been developed to help clinicians around the world make sense of complex scans using artificial intelligence.”

Samantha Fitzsimmon, Project Manager, John Walton Muscular Dystrophy Centre

Over £1.5m

invested into the NorthStar programme over the past 20 years

£1.15m

invested in a new strategic award for mitochondrial disease research

£1m

invested in a new strategic award for Charcot-Marie-Tooth disease

12

new grants worth over £1.7m committed this year

43

active research projects

£19,000

invested in a new grant scheme for improving quality of life

Over 100

people contacted our research line

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Driving change for access to specialist care and support

We successfully worked to secure access to treatments for muscle wasting conditions this year. At the same time, we continued to support healthcare professionals by upskilling them in the needs and care of our community while also providing them with networking opportunities. We also ensured NHS neuromuscular services received appropriate attention from commissioners and decision makers.

1 new treatment approved for NHS use

8 treatment assessments participated in

Our role in treatment recommendations and appraisals

people living with Duchenne muscular dystrophy right across the UK.

711

enrolments to our e-learning module

Connecting and upskilling healthcare professionals

177

attendees at our two conferences

This year, we continued to work tirelessly to ensure that once new and effective treatments are found people with muscle wasting conditions can access them. We championed the voices of our community in eight assessments that determine whether new treatments should be made available on the NHS. By working closely with people affected by muscle wasting conditions, healthcare professionals, researchers, other charities, and patient groups, we made sure lived experiences were at the heart of every discussion. We also supported and empowered patients, families and carers to contribute as expert voices in these vital decisions.

Our healthcare

professional conferences

266

We continued to support our healthcare professional community this year, organising conferences for professionals involved in the care and support of people living with muscle wasting conditions, providing them with the opportunity to upskill, share best practice, and network.

attendees at our three healthcare professional upskilling webinars

topics of travel, sexuality and relationships, along with increasing attendees’ understanding of the welfare benefits and employment systems, housing provision, and education. This holistic knowledge is extremely important for care advisors in supporting the physical and emotional needs of people living with a condition and in acting as coordinators across all aspects of their health and social care.

Our Neuromuscular Care Advisor Conference

It was another successful year for our Neuromuscular Care Advisor Conference, with 51 care advisors and clinical nurse specialists attending from across the UK. The conference focused on quality of life for people living with a muscle wasting condition through the

We’re especially proud to have played a key role in securing NHS access to a new treatment, vamorolone (Agamree), for

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Our Allied Health Professional Conference

Our Allied Health Professional Conference brought together 126 allied health professionals both in-person and online, in a hybrid conference model, this year. The conference covered a wide range of topics such as physiotherapy management, respiratory care, wheelchair seating recommendations, condition-specific upskilling of myasthenia gravis, and ways of multidisciplinary team working in supporting patient care and partnering with health and social care professionals in the community. Accessing specialist therapists is important to our community. This programme of upskilling and supporting allied health professionals working with people living with muscle wasting conditions to maintain and improve the quality of care provided is an important aspect of our work.

Upskilling webinars

This year we provided CPDaccredited upskilling webinars to 266 healthcare professionals, including specialist neuromuscular professionals and non-neuromuscular specialists such as GPs and A&E staff. For specialist neuromuscular professionals, webinars were provided to upskill their understanding of mental health and wellbeing of people living with a muscle wasting condition. For nonneuromuscular professionals, webinars provided a more general understanding and awareness about muscle wasting conditions. A further 642 professionals received resources from these webinars.

Centre of Excellence awards

Following on from the decisions of our 2023/24 Centre of Excellence audit, we spent this

year conducting engagement we launched a community visits to 19 adult and paediatric survey to discover more about neuromuscular centres. These what our community would like visits provided an opportunity us to prioritise in our policy and to present awards and campaigning work. We received strengthen our relationships almost 700 responses from with neuromuscular services people living with a muscle and their NHS Trust. They also wasting condition, their families provided room to discuss and carers. In May 2024, we the challenges faced by published the results of this neuromuscular services and survey. This vital community what we as a charity can do feedback has informed our to support. new and updated position statements on the biggest Combined with this, we also priorities for our community, produced a report analysing the around awareness of muscle outcome from our 2023/24 audit, wasting conditions, access with the data providing a unique to healthcare, and financial insight into the current state of security. We will continue neuromuscular services. Our in-depth engagement going audit found many examples forwards to ensure our efforts of excellent achievements by to drive change are focused neuromuscular teams across on the issues that matter the UK, with their high level of most to our community.

Combined with this, we also produced a report analysing the outcome from our 2023/24 audit, with the data providing a unique insight into the current state of neuromuscular services. Our audit found many examples of excellent achievements by neuromuscular teams across the UK, with their high level of dedication and commitment. However, it also showed the challenges facing services due to current pressures in the NHS.

Reporting on the financial insecurity of our community

Financial security emerged as one of the leading concerns (49% of respondents) in our community survey. This led us to explore this further; writing and publishing a report on the financial insecurity of our community, which was published in November 2024. The Financial Insecurity Report was based on 400 survey responses, as well as interviews and case studies with people living with a condition. It highlighted a decline in financial wellbeing since last year and revealed that 53% of people living with a muscle wasting condition feel financially insecure, 17% of whom feel very insecure. The report also showed the widespread negative impact this can have on people’s physical and mental health, ability to work, and quality of life. This all provided crucial evidence and stories to help us influence government policy, particularly at a time when support for disabled people is under threat.

Sharing of sensible, expert approach to supporting children with neuromuscular disease, which will make my job as a general paediatrician easier and safer in emergencies.”

Webinar participant

Our policy and parliamentary work

Community survey - setting out priorities

A central part of our mission is to campaign for people’s rights, better understanding, and accessibility. Last year,

One of the biggest expenses for us is our energy bills which we spend roughly half our income on. We both have air mattresses to ensure we don’t get pressure sores, we have four ventilators between us, which are running or charging 24 hours a day, two wheelchairs which need to be charged regularly, to name just a few things.”

Charlotte and Tom, case study from our Financial Insecurity Report

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Muscular Dystrophy UK Annual Report | 21

Living well

We understand that living with a muscle wasting condition can be overwhelming and isolating for people affected and their families. This is especially true if they don’t have access to the right information and support to help them live well. We’re here to listen and provide information and advice about all aspects of living with a muscle wasting condition.

Our helpline service

Our advocacy service

This year 3,392 people contacted our helpline. Our team provided tailored information and emotional support to people living with a condition, their family, carers and friends. Delivering advice and support by phone, email, face-to-face, or through a referral from NHS neuromuscular clinics. The five topics people most contacted us about were alert cards, peer support, welfare information requests, medical questions, and equipment advice.

We supported 133 people through our advocacy service this year. Supporting them to express their views and wishes and to challenge decisions made about them in relation to things like access to care, equipment, benefits and education. Helping people to develop self-advocacy skills in the face of these challenges and clearly communicate their needs and rights. The most support we provided was on Personal Independence Payment (PIP), housing and adaptations, and care packages.

The challenges felt like being in a maze, but I called the helpline, and they answered so many of my questions and supported me through the process.”

Lauren, living with SMA type 1

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Mobility equipment grants

Our tailored peer support

This year, we provided 131 grants for the cost of mobility equipment through our grant giving arm the Joseph Patrick Trust to people living with a muscle wasting condition. We also collaborated with two other grant providers, Whizz Kidz and SMArt Moves, to jointly fund power wheelchairs.

Our peer support groups continue to flourish. In the past year we’ve facilitated support groups based on condition, age or circumstances, such as recently receiving a diagnosis. We’ve also worked in partnership with the Teapot Trust, a mental health charity providing art therapy for children and families living with long term health conditions, to pilot a support programme for primary school aged children living with muscle wasting conditions.

Our tailored therapeutic support groups

Following the successful launch of our therapeutic support groups in 2023, we partnered with Louise Halling, a professional counsellor and psychotherapist living with limb girdle muscular dystrophy, and Julie Oates, a counsellor and psychotherapist, to continue to deliver virtual therapeutic support groups. These sessions provided a confidential, supportive space to foster open discussions and build connections. Ten therapeutic groups took place over the year covering newly diagnosed, mums, dads, partners, grandparents, siblings, and parents of children living with a condition.

Our peer support WhatsApp groups have grown significantly and are now a core part of our support services. Moderated by staff and volunteers, these groups enable peer connection, shared experiences, and timely guidance, supporting members in managing their condition.

Alongside these new groups, we continue to offer one-to-one peer support from our trained peer support volunteers with lived experience.

3,392

people supported through our helpline

Over 130

people supported through our advocacy service

More than 200

people attended our information days across the UK

462

people joined our WhatsApp communities

447

people attended our Muscle Groups

109

referrals supported by our peer volunteers

62

peer volunteers in our volunteer network

131

people provided with a wheelchair and other equipment grants

22 | Muscular Dystrophy UK Annual Report

living with muscle wasting conditions. These events provide an opportunity for people to connect with others in the muscle wasting community, share stories, hear from experts to help them live well, meet our team, and find out more about the advice and support we offer.

Muscle Groups – keeping people updated and connected

We ran 37 Muscle Group meetings this year across 14 regions of England, and in Scotland, Wales and Northern Ireland. A total of 447 people attended a local meeting. Our regional Muscle Group meetings provide a safe, welcoming space where people affected by muscle wasting conditions can share experiences, meet other people in their local community, and learn more about the services we offer.

PIF accredited for trusted health information

Following our second-year assessment with the Patient Information Forum (PIF), we’re proud to be successfully recertified under the PIF TICK Quality Mark for Health Information as a producer of trusted information. The PIF TICK logo now features on our health information providing assurance that our content is evidence-based, accessible, and produced to the best possible standard.

Our webinars

We held seven webinars this year, providing research updates, condition-specific information and practical and lifestyle talks to help people live well with their condition. Condition management topics included cardiac management, physiotherapy, emotional support, speech and language therapy, and diet and nutrition. Our webinar sessions focused on Duchenne muscular dystrophy, FSHD, nemaline rod myopathy, Becker muscular dystrophy, LMNA, myotonic dystrophy, and limb girdle muscular dystrophy.

Our Employability Programme

Our Employability Programme provided 162 interactions of support over the past year. The three main areas supported by the service are career advice, application support, and workplace advice for those already in work. We also launched a workplace adjustment passport, which gives people with any disability a way of communicating their workplace needs with their employer and to put a plan in place. This can be taken with someone as they change roles, or their manager changes.

Our Information Days

We held four in-person Information Days/conferences in England, North Wales and Scotland as well as a disability sports event and some holistic physiotherapy events. Bringing together a total of 209 people

My overarching takeaway is that I am not alone and there is great support available.”

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Muscular Dystrophy UK Annual Report | 23
Photographer: Chris Fairweather/Huw Evans Agency
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Information Day participant

24 | Muscular Dystrophy UK Annual Report

Muscular Dystrophy UK Annual Report | 25

Our work in Scotland

We work in each of the four countries of the UK. We’re required to provide a report on our activities in Scotland by the Office of the Scottish Charity Regulator.

for families to connect with one another and learn more about our support in Scotland.

We significantly expanded our reach and impact across Scotland this year, ensuring more equitable and accessible support for people living with a muscle wasting condition, their families and carers. We welcomed two new members of staff to our Scotland team, one covering Central Scotland and the other supporting the North – they joined our Head of Regional Support, Outreach, and Information. This expansion has allowed us to offer tailored support across a broader geographic area, including remote and rural communities.

Neuromuscular

physiotherapist sessions

Between September 2024 and January 2025, we delivered a hybrid series of four in-person and virtual sessions for adults living with muscle wasting conditions, in collaboration with a specialist neuromuscular physiotherapist in central Scotland. Each session explored a key area of wellbeing, including fatigue and sleep management, physical activity and posture, nutrition, mental health, and navigating benefits, housing, and care systems.

Our support services

Our support services in Scotland are wide-ranging and holistic, providing emotional support from the point of diagnosis continuing through every stage of living with a muscle wasting condition. We also offer practical assistance to help people make informed decisions and access the services and entitlements they need to live well. This year, we responded to 426 support requests across Scotland, including 50 advocacy cases.

Missing People. Missing Support report

In November 2024, we launched our new Missing People. Missing Support report shining a light on the gaps in neuromuscular care in Scotland and advocating for stronger, more consistent support across the country.

Scotland Information Day

We were delighted to host our Scotland Information Day in Inverness in March 2025. Families from the North of Scotland came together for a day of education, support, and community. Sessions covered physiotherapy, fatigue management, emotional wellbeing, and adaptive sports.

Scottish disability sports

In August 2024, we once more partnered with Scottish Disability Sport to host a free family sports day at Grangemouth Sports Complex. Children under 18 had the chance to try adaptive sports like curling, boccia, and swimming in a supportive and inclusive environment. This event not only encouraged physical activity but also created valuable opportunities

Our work in Scotland continues to be shaped by the invaluable insight and experience of our Scottish Council.

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Photographer: Phil Wilkinson
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Fundraising update

Family Funds

year, and a total of nearly £40,000 since its inception.

Two new family funds joined us this year, taking our total in Scotland to eight. Vanessa from Shetland hosted a Bake a Difference fundraiser raising a phenomenal £13,000 for research into Facioscapulohumeral muscular dystrophy (FSHD), the condition her five-year-old daughter Phoebe lives with. Their efforts didn’t stop there. Vanessa has since launched their Family Fund, Phenomenal Phoebe, ensuring that both fundraising and awareness will continue to grow in support of Phoebe and others like her.

We have seen a huge uptake for our Scotland events including Kiltwalk where we had 32 participants across the four different cities raising around £12,000. Supporters used these events to fundraise and raise awareness about muscle wasting conditions. Back in August we held a really successful Zipslide across the Clyde as one of our supporters Sophie, 21, who lives with limb girdle muscular dystrophy, took on the event with eight friends and family members and raised a fantastic £8,000.

Community fundraising activities

Our total fundraising in Scotland

An array of supporter led activity has contributed to our fundraising total this year; however, the Spirit of Christmas continues to be our stand-out event, raising £4,800 this

Our total fundraising in Regional Development for Scotland was £143,813 this year – an increase of £7,221 from 2023/24.

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462
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support requests responded to this year, 50 of which were for advocacy support

£143,813

total funds raised

£12,000

raised through Kiltwalk by 32 participants

Research

We continued to support research in Scotland this year. We are now funding Dr Jarod Wong at the University of Glasgow as part of our 2024 grant round. While our funding continues to support a PhD student in the laboratory of Dr Lyndsay Murray and a research project with Professor Tom Gillingwater at the University of Edinburgh.

‘We significantly expanded our reach and impact across Scotland this year’

Muscular Dystrophy UK Annual Report | 27

The difference

your support made

Thanks to your amazing generosity, income from donations, gifts, grants, sponsorship, events and campaigns totalled £4.5m this year.

Highlights of this year’s fundraising

Celebrating our Microscope Ball’s 40th anniversary

Climbing Mount Kilimanjaro to raise funds

We were extremely grateful this year to the 720 members of the commercial property sector who brought the 80s back to life at London Hilton on Park Lane by attending our 40th Microscope Ball anniversary event. We raised an event record of over half a million pounds on the night, thanks to our incredible pledge speaker Lou Hill, Trustee James Lee, our fantastic host Miss Demeanour, the amazing Globe Star Entertainments for their unforgettable performances, auctioneer Jonny Gould, and of course, our amazing Microscope Ball committee and chair Michelle Anthony.

In October 2024, 15 incredible supporters travelled to Tanzania to take on the life-changing challenge of climbing Mount Kilimanjaro – the highest peak in Africa – in support of the charity. Over the course of six tough and demanding days, the team faced altitude, exhaustion, and extreme conditions. Pushing themselves to the limit to increase awareness and raise a remarkable £85,500 (£101,000 including gift aid).

A record-breaking year for our Bidwells Town and Gown series

A landmark year for our Bidwells Town and Gown 10K running series, this year we had both record-breaking participation and fundraising across our Oxford and Cambridge events.

Our running events are booming

In May, our Oxford Bidwells Town and Gown 10K sold out for the first time in its history, with over 5,600 runners raising more than £245,000 for the charity. Just a few months later in October, the Cambridge event welcomed 2,978 participants, just 22 places away from capacity, and raised an impressive £113,000 – its highest total to date.

In 2024, 8,994 participants took part in 41 different running events – from 5ks, 10ks to some of the most sought-after marathons – across the UK and internationally raising a phenomenal £1.2m for the charity.

76

Trusts and Foundations supported our work this year

£1.2m

raised across 41 different running events

£176,000

raised from our 43 Family Funds

Over

£500,000

raised at the 40th Anniversary Microscope Ball

£245,500

raised at a sellout Bidwells Oxford Town and Gown 10k

£101,000

raised by 15 supporters climbing Mount Kilimanjaro

£80,000

raised in just three days through Double your Donation

£74,157

It was the most amazing six days of our lives. It tested every single ounce of mental and physical strength. To do it with other people who are raising money for MDUK has been really rewarding.”

Simon, who climbed Mount Kilimanjaro

raised from activities related to our RHS Chelsea Flower Show Garden

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London Marathon 2024 – A record-breaking year

Strength to strength – our Pedal Paddle Peak triple challenge events

Supporters fundraising their way

A record 172 runners took on the TCS London Marathon in support of the charity this year – our largest team to date. Together, they raised an incredible £580,000, the highest total ever raised for the charity through a single event.

Our Pedal Paddle Peak flagship triple adventure challenge continued to go from strength to strength this year. We not only celebrated the ninth successful year of our Lake District event, but also launched a brand-new edition in Snowdonia, expanding the series and growing our participation.

date. Together, they raised an Supporters from across the

incredible £580,000, the highest UK continued to show their total ever raised for the charity incredible commitment through a single event. this year by fundraising in

We also secured 160 places for their own unique ways.

the 2025 event, including two From bake sales, zip slides assisted wheelchair entries for and personal challenges, members of our community – we’re always blown away a step towards a more inclusive event and shaping the 2025 by our community finding event to be another special one. new and unique ways to raise awareness and funds. Highlights of their inspirational fundraising include:

In the Lake District, 150 participants raised over £115,000 (including gift aid). This marked the second consecutive year the event raised over £100,000, a sign of the event’s growing popularity.

Our inaugural Snowdonia challenge welcomed 64 adventurers who raised an impressive £62,500 (including gift aid) in the event’s first year. This new location proved a huge success and lays the foundation for continued growth of the series.

Eight marathons in eight weeks

Tom Penzer Adams ran eight marathons in eight weeks in support of his close friends, Gary and Paul, who live with limb girdle muscular dystrophy. In total, he ran over 209 miles and raised over £17,000 from this mammoth challenge, which saw good luck messages from the likes of Mo Farah.

With the growing success of these events, we’re laying the way to increase participation at both events and explore a third location over the next few years to form a Pedal Paddle Peak trilogy.

This team was by far the best team I have ever had the pleasure to run for. The communication and support were excellent!”

Three peaks in memory

In April 2024, nine friends tackled the Yorkshire Three Peaks Challenge in memory of their school friend Simon Mirfin, who lived with Facioscapulohumeral muscular dystrophy (FSHD) and sadly passed away in 2023. Their heartfelt tribute raised over £7,900 to honour Simon and support other people living with muscle wasting conditions.

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Cycling across Europe

Tim Norton, 68, flew to Gibraltar to undertake a 1,700 mile cycling adventure across Europe travelling through the likes of Spain, over the Pyrenees, through France and back to his

hometown in Lancashire. Tim raised in excess of £2,300 in support of his friend Andy who lives with Facioscapulohumeral muscular dystrophy (FSHD)

Coast to coast for Josie

The Chubbs Crusade Family Fund took on and completed their very own challenging 84 mile coast to coast trek from Bowness-on-Solway on Cumbria’s West Coast to the East Coast of Northumberland in Newcastle upon Tyne, completing the challenge in just two days. James Chubb and five friends raised over £13,000 in support of James’ daughter Josie, seven, who lives with Ullrich congenital muscular dystrophy.

Golf days – driving strong support

Golf days continue to be a popular way for our supporters to raise funds and awareness. In 2024, events were held across the UK. From our very own Property Golf Day at the Centurion Club in Hertfordshire to supporter-led days organised by the Evans Family in the West Midlands, Family Fund Fighting Back for Jack 10th annual golf day also in the West Midlands, and David Salt’s golf day in Staffordshire. Together, these fantastic events raised an incredible £100,500 to support our work.

Star-studded comedy night

Our Hywood’s Heroes Family Fund once more organised a night of comedy with seven comedians led by Jon Richardson. Coming together to entertain an audience of over 1,000 people at Aylesbury Waterside Theatre and raise over £43,000. The money raised from the night, and other fundraising activities, brings the phenomenal total raised by Hywood’s Heroes over the last six years to over £300,000.

Our Family Funds

Strategic Solutions, and didn’t stop there – recruiting a London Marathon runner, volunteering at the MDUK Celebrity Sports Quiz, and hosting GNE Myopathy coffee mornings. In her first year alone, Tahira has raised over £10,000.

Our Family Funds are an incredibly important part of our community. We have 43 active Family Funds who this year raised an impressive £176,000 between them by organising their own events, encouraging their networks to take part in challenge events, as well as national campaigns and appeals. Their ongoing efforts are truly invaluable.

Our Family Fund Weekend

In September 2024, we bought together families from our Family Fund network at the Barnstondale Centre in Wirral for our annual Family Fund Weekend. The event offers a warm, welcoming space for families to unwind, connect with others who truly understand, and make lasting memories.

Welcome Tahira’s Team

In 2024, we were delighted to welcome Tahira’s Team to our family funds. Tahira nominated the charity as Charity of the Year at her workplace, Optimum

“Just such a brilliant weekend full of precious memories which we really appreciate from the bottom of our hearts.” – Family Fund Weekend 2024 attendee

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RHS Chelsea Flower Show success

We were hugely fortunate to have a garden at the 2024 RHS Chelsea Flower Show this year. Our Japanese-inspired Forest Bathing Garden was designed by Ula Maria, 2017 RHS Young Designer of the Year, and fully funded by Project Giving Back, a charity who fund gardens for good causes at the show. Not only was the garden a gold medal winner but was also awarded the coveted Best in Show Garden. Winning both these titles led to us receiving unprecedented media coverage and visits to our website more than doubled.

Raising awareness with non-neuromuscular healthcare professionals

The Muscular Dystrophy UK Forest Bathing Garden is a peaceful, accessible garden, created with people living with a muscle wasting condition, their families and carers, and clinicians in mind. Following the RHS Chelsea Flower Show the garden has been relocated to the Prince and Princess of Wales Hospice in Glasgow where it will provide a unique outdoor space for patients, their families, and the local community to benefit from.

We were able to use our platform at the Show to act on a priority from our community survey findings, which is to increase awareness of muscle wasting conditions among non-neuromuscular specialist healthcare professionals. We invited over 100 GPs and other healthcare professionals to an engagement and networking event at the show. This included talks from experts in neuromuscular care, networking opportunities with people from our community, an opportunity to talk to staff about Maximising the opportunity the training we offer to upskill We were determined to healthcare professionals, along maximise the opportunities with details about our Regional our garden offered us in Neuromuscular Networks. engaging existing and new audiences to increase our The Medical Director for reach and awareness of Professional Development muscle wasting conditions. at the Royal College of We did this through activities General Practitioners (RCGP) which included running ticket attended and spoke about competitions, hosting business the importance of taking breakfasts for key supporters part in e-modules for and their networks, and neuromuscular conditions. organising after hours receptions for sponsors and non-neuromuscular specialist healthcare professionals.

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Connecting with the muscle wasting community

Many visitors were moved by our garden. Our volunteers took time to speak to them and when a connection to our cause was discovered, they were invited onto the garden. We heard stories of family, friends and neighbours of people living with a condition who were appreciative and delighted that muscle wasting conditions were being represented on a national stage. On the final day of the show, we let all wheelchair users, and those with mobility issues, onto the garden. The impact of the garden being fully accessible was fully realised and our disabled visitors felt the joy of experiencing something designed just for them.

Immeasurable impact, exceeding expectations

There is no doubt that the garden funding from Project Giving Back achieved our aims of raising awareness of muscle wasting conditions. The opportunity gave us a huge uplift in social media and media coverage, enabling more people to find out about our work. What was also surprising was the impact it had on our existing supporters. Many supporters who donate regularly doubled their donation immediately after the show, and members of our events committees – who already give up lots of their time to organise fundraising events - did even more, with some signing up for challenges such as the London Marathon and trekking Kilimanjaro. All 2024/2025 challenge events in our portfolio sold out early, which we also put down to the ‘Chelsea effect’.

Photographer for both: Rebekah Kennington

There are still so many people who have never heard of muscular dystrophy, so it’s amazing the charity has been given the opportunity to raise awareness in such a high profile event”

Our President’s Award winners

These annual awards recognise outstanding people doing remarkable things to make muscles matter. This year’s winners are:

Early Career Scientist of the Year Award

Peter and Nancy Andrews Community Achievement Award

Dr Ami Ketley

Liz Keenan

Based at the University of Nottingham, Ami recently secured one of our research grants to study genetic variations in different tissues of people living with myotonic dystrophy. Using new technology called single-cell transcriptional profiling, results should highlight which potential genes could be targeted for treatments. Ami is also a Trustee of the Myotonic Dystrophy Support Group and actively engages with the patient community.

A devoted mother, fundraiser and advocate, Liz has tirelessly campaigned for the charity while raising her three boys, all of whom live with Duchenne muscular dystrophy. Always up for a challenge, she has tackled some of our demanding fundraisers, including our Pedal Paddle Peak triple challenge event. Over the past decade, Liz and her family have raised over £100,000 to support our work.

Fundraiser of the Year Award

Volunteer of the Year Award

Phil Grant

Tom Penzer Adams

Inspired by two friends who live with a muscle wasting condition, Tom set out to run eight marathons in eight weeks to raise £8,000 for us. His challenge saw him travel around the UK as well as taking part in overseas marathons in Tokyo and Boston and organising a community marathon event in his hometown. In total, he ran 209 miles and raised over £20,000.

Well known for appearances in his local area dressed as Wonder Woman, Phil has been fundraising and volunteering for us since 1992. He does this in memory of his son who lived with Duchenne muscular dystrophy, to raise awareness to help others. He already has a long list of Wonder Woman appearances booked for 2025.

Alexander and Valerie Patrick Award for Carer of the Year

Richard Attenborough Award for Outstanding Achievement

Sheila Hawkins

Isabel Spragg

A former charity Trustee, Sheila sits on our Services Development and Improving Quality of Life Research Committees and is also President of FSHD Europe. Living with Facioscapulohumeral muscular dystrophy (FSHD), Sheila brings invaluable lived experience and is a dedicated supporter and volunteer.

A remarkable young carer, 13-year-old Isabel goes above and beyond to support her brother Harry who lives with Duchenne muscular dystrophy. Helping Harry with day-to-day activities like dressing, washing and feeding, as well as just making him laugh, Isabel’s support is invaluable to her family.

Community attendee

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Muscular Dystrophy UK Annual Report | 35

Our finances How we raised our funds

£1 For every we spent:

is invested in fundraising to ensure we maintain a diverse portfolio to 32p support our community is spent on our charitable activities 68p

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£1 £2.50
For every we invested in fundraising we raised
(total income / fundraising costs)
£1 50p
£1
£1
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10%
25%
33%
£7.9m
10%
9%
11%
2%
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----- Start of picture text -----
32% 32%
£10.1m
13%
23%
4%
22%
41%
£11.8m
34%
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Total income

Events and promotions (£2m)

Individual giving (£802,000)

Major Donors and Corporate (£678,000)

Trusts

(£193,000)

Regional development (£873,000)

Legacy (£2.6m)

Other income (£821,000)

Total expenditure

Fundraising

(£3.2m)

Medical research (£2.3m)

Access to specialist care and support (£1.3m)

Independent living (£3.2m)

Total funds

Designated (£4.8m)

General (£4m)

Restricted (£2.5m)

Endowment (£415,000)

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Muscular Dystrophy UK Annual Report | 37

Our future plans

In 2025, we’ll be publishing an ambitious new strategy to improve the lives of people living with muscle wasting conditions over the next ten years.

We will be focusing on four strategic goals:

Strategic goal one Transforming diagnosis

Strategic goal two No one faces their journey alone

Misdiagnosis and delays to diagnosis mean people living with muscle wasting conditions can miss out on vital treatment and support and feel more alone with their condition. For some conditions, newborn screening can have life-changing benefits allowing for early diagnosis and faster access to treatment that can radically transform lives.

Getting the right support at the point of diagnosis can be crucial to living well with a condition. Yet too many people face this journey alone.

We’ll reach every person with a muscle wasting condition by 2035, so no one faces this journey alone.

How we will do it – our focus for the first three years:

We’ll help speed up and improve the accuracy of diagnosis so that by 2035, no one will wait longer than six months to be diagnosed.

How we will do it – our focus for the first three years:

reach into neuromuscular centres

• We will significantly increase

Strategic goal four Living life to the full

Strategic goal three New treatments, universal support

For the first time new treatments are being developed which can slow the progression or reduce the impact of some conditions. However, too often people are unable to access them due to a lack of capacity in the NHS. While some areas of the UK have specialist clinical support local to them, there is a stark postcode lottery in the availability of services for people living with muscle wasting conditions. This means that some people miss out on the care and support needed to help them live well with their condition.

Living with a muscle wasting condition can lead to poor physical and mental health. People living with muscle wasting conditions also face huge societal barriers to living a full and independent life, including inaccessible transport, housing, education and employment.

We’ll campaign for a more equal and accessible world and directly support every person who needs it by 2035 to live independently with better physical and mental health.

How we will do it – our focus for the first three years:

We’ll help accelerate the development of new treatments so that by 2035 they’ll be available everywhere, and everyone living with a muscle wasting condition will be able to access specialist support when and where needed.

How we will do it – our focus for the first three years:

Our vision is clear, a world without limits for people with muscle wasting conditions, and we won’t stop until we achieve it.”

Andy Fletcher, Chief Executive

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Thank you

Our President

Honorary Life Presidents

Our Patrons

Research Vice Presidents

• Professor Sir Douglass M Turnbull MBBS (Hons), MD, PhD, FRCP

Vice Presidents

of Winchester MBE

Our Trustees

Senior Leadership Team

• Andrew Fletcher, Chief Executive (from November 2024)

• Wojtek B Trzcinski, Chief Operating Officer / Interim Chief Executive (June 2024-November 2024)

• Rob Burley, Director of Care, Campaigns and Support (until December 2024)

• Neeru Naik, Director of Services and Support (from January 2025)

With special thanks

Corporate Support

Golf Day Committee

Charity Shoot Day Committee

Joseph Patrick Trust Management Panel

Strike Night Committee

• Lynn Smith

Joseph Patrick Trust Grants Panel

Sports Quiz Committee

Trusts and Foundations

Finance Committee

Microscope Ball Committee

40 | Muscular Dystrophy UK Annual Report

Appointments and Remuneration Committee

Medical Research Committee

Improving Quality of Life Committee

Lay Research Panel

Services Development Committee

Northern Ireland Council

Scottish Council

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Our policies

Fundraising statement

Our supporters are key to changing the future of muscle wasting conditions, and in observing and promoting a consistently high standard of fundraising. We regularly monitor our practices to identify training requirements and set policy priorities for our fundraising. We work to ensure a culture of honesty, integrity and respect with the public, as well as transparency of process to our donors about our cause and the way that their donation will be used. We also recognise how important it is to manage our supporters’ data compliantly, with both care and integrity. Our statement of fundraising best practice underlies our commitment to the following personal information practices:

These actions enable us to protect vulnerable people and all other members of the public from any behaviour that could be deemed:

We offer many different opportunities for our fundraisers and donors to engage with us to allow us to fulfil our charitable objectives. These include special and challenge events; corporate partnerships; trusts and foundations; regional and community fundraising activities, including Family Funds; fundraising groups, branches and events; individual giving, which includes regular giving, major gifts, appeals, raffles and a weekly lottery, membership scheme; Christmas cards and online shop sales; legacy and in-memory programmes.

We conduct the following through commercial participation agreements: payroll giving, our gaming programme, legacy administration, the shop fulfilment, print and mailing houses for external mailings, and most of our regional and national challenge events. We monitor our third-party providers and operate due diligence checks to ensure best practice. We also carry out internal analysis to ensure the work delivered by these agencies provides best value to the charity, its supporters and users.

We are paid-up members of the Fundraising Regulator and subscribe to the Fundraising Codes of Practice. We have ensured staff remain up to date in all areas of fundraising, governance and training through mandatory online training as well as seminars and events by relevant providers.

We received three complaints in total in 2024/25. These are included in the following: 0

complaints from 16,021 mailings about our lottery and raffle to warm supporters; 0 complaints from 1,047 guests at our series of special events; 0 complaints from 407 participants at our National Third Party Challenge Events; three complaints from 8,824 participants at our own running events (Bidwells Town and Gown and Pedal, Paddle, Peak), 0 from 400 volunteer fundraising events; 0 from 43,773 pieces of direct mail sent out; 0 complaints from 6,015 pieces of mail sent out about gifts in Wills. We have worked together with the individuals who made the three complaints mentioned to ensure we will learn from our mistakes for the future.

Financial review and policies

Our total income for 2024/25 was £7.9m, compared to £9.5m in 2023/24. The £1.6m decrease is primarily due to the conclusion of the Government-funded Changing Places programme and one-off grants such as the Chelsea Flower Show, both recognised in the previous year. Additionally, there was a natural variation in legacy income.

Fundraising income from donations, gifts, grants, and other activities remained stable at £4.5m.

Legacy income decreased by 11% to £2.6m (2023/24: £2.9m), reflecting normal fluctuations in this income stream. This figure includes a £1.4m accrual based on best estimates of future receipts.

Other income, including investment and trading, totalled £820,000 (2023/24: £1.3m). Government grants amounted to £15,000 (2023/24: £847,000), as expected, due to the end of support from the UK Government’s Covid Medical

Research Charity Support Fund, the Department for Transport, and the Department for Levelling Up, Housing and Communities.

Total expenditure on charitable activities rose by £2m (25%) to £10m (2023/24, £8m). This increase was spread across all areas but primarily driven by the final distribution of Changing Places grants.

Breakdown of charitable expenditure:

The shift in proportions reflects the final allocation of Changing Places funding, which was fully attributed to Independent Living.

The charity ended the year with a planned deficit of £2.1m (2023/24: surplus of £1.9m), including a £109,000 gain on investment assets (2023/24: £442,000 gain). The reported surplus figure includes the £1.4m legacy accrual, expected to be received in future years once legal matters are resolved.

Reserves policy

Free reserves available to the charity exclude restricted, endowment, and designated funds, as well as tangible fixed assets held as unrestricted funds. The charity considers it essential to hold free reserves to provide sufficient protection to cover core costs, including salaries and central overheads, and to meet forward unrestricted commitments in the event of an immediate or unforeseen drop in income.

The recommended level of free

This fund will cover anticipated deficits over the next two to three years, including the budgeted deficit of £1.5m for 2025/26, thereby protecting the free reserves of £4m.

reserves is reviewed annually anticipated deficits over the by Trustees and the Senior next two to three years, Leadership Team (SLT) as part including the budgeted of the budget-setting process, deficit of £1.5m for 2025/26, considering the financial impact thereby protecting the free of current risks facing the charity. reserves of £4m. The charity aims to maintain a certain level of free reserves to • Strategic Research Grants manage the risks it is exposed – £1.6m – designated for two to in the course of its operations, five-year research initiatives: including but not limited to LifeArc Centre to Treat fluctuations in voluntary income. Mitochondrial Disorders (Cambridge University) and Following a strategic review Trial Readiness for Charcotaligned with our future growth Marie-Tooth Disease ambitions, the free reserves (University College London). requirement has been The balance on 31 March increased to reflect six months 2025 represents the fund of operating costs, now set value after £540,000 of this at £4m. fund was distributed during The rationale for this decision the 2024/25 financial year.

The rationale for this decision is based on three key factors:

Free reserves (£4m)

The total unrestricted funds balance of £8.8m on 31 March 2025 includes:

Designated and fixed assets (£4.8m) set aside for specific strategic purposes:

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Muscular Dystrophy UK Annual Report | 45

Having reviewed the strategic risks and the 2025/26 budget projections, the Board of Trustees considers the reserves held as of 31 March 2025 to be sufficient to manage these risks effectively. Accordingly, the Trustees continue to adopt the ‘going concern’ basis in preparing the Annual Report and Accounts.

Investment policy

The overall objectives are to create sufficient income and capital growth to enable the charity to carry out its purposes consistently year by year with due and proper consideration for future needs and the maintenance of, and if possible, the enhancement of, the value of the invested funds while they are retained. The portfolio aims to achieve a return several percentage points over the annual increase in the Consumer Price Index, over the medium to long term. Both capital and income may be used at any time for the furtherance of the charity’s aims. The objectives are to be achieved by investing prudently in a broad range of fixed interest securities and equities, which are quoted on a Recognised Investment Exchange, and Unit Trusts and OEICs (open-ended investment companies), which are authorised under the Financial Services and Markets Act 2023. There should be no direct investment in the following: derivative contracts, including futures and options; commodities and derivatives thereof, contracts for differences or structured products. The charity maintains a balanced risk profile, seeking moderate growth with a diversified portfolio. The portfolio is managed to avoid excessive volatility and to ensure liquidity for operational needs.

The investment portfolio is managed by Rathbones’ Charity Multi Asset Team, supported by

experienced professionals. The charity’s Finance Committee reviews performance quarterly and ensures alignment with strategic objectives. The investment managers’ performance is reviewed by the Finance Committee on an annual basis. This policy is reviewed annually and updated as necessary.

Ethical considerations

Environmental, Social, and Governance (ESG) factors are integrated into the investment process. The charity supports investments in sectors such as diagnostics, medical devices, software, and financial services that demonstrate strong ESG credentials. The Charity does not invest directly in tobacco, armaments, high-interest rate lending, gambling, adult entertainment, thermal coal and tar sands (defined by companies which derive >10% of their revenue from these).

In 2023/24, Trustees have reviewed the approach of the fund manager towards avoiding offenders in greenhouse gas emissions. It is felt their approach continues to be sufficient. Trustees reserve the right to exclude companies or industry sectors that carry out activities contrary to the aims of the charity, or from holding particular investments that damage the charity’s reputation. Trustees expect the fund manager to have considered the suitability of investments of the same kind as any particular investment proposed or retained.

In 2024/25, Trustees and the SLT confirmed that the fund manager was not investing in Russian businesses following the Russian invasion of Ukraine in February 2022.

Renumeration policy

Salaries for the Chief Executive and the SLT are set by the Board’s Appointments and

Remuneration Committee. This process takes into account the overall performance of the charity, external benchmarking, and the long-term needs of the organisation.

The charity is committed to fair pay and pays above the London Living Wage for all roles. Vacancies are advertised on our website and external recruitment platforms, with applications welcomed from both internal and external candidates. Some roles can be advertised only internally before opening external candidates when no suitable internal candidates come forward. Recruitment agencies are used when direct recruitment proves difficult.

No member of the SLT receives a car allowance or vehicle from the charity. All staff and Trustees travel on standard fares when undertaking charity business. Trustees do not receive any remuneration or other benefits for their work. Details of reimbursed expenses to Trustees are disclosed in Note 18.

In 2024/25, the charity undertook a comprehensive benchmarking exercise across all staff salaries. To ensure competitiveness and fairness, the recommendations from this review were implemented in June 2025.

Risk management

The Trustees continue to support formal risk management procedures to assess business risks and implement strategies to mitigate them. Risks are identified and classified based on their potential impact and likelihood, with appropriate controls and processes in place to manage them.

The charity operates a comprehensive risk management strategy underpinned by a detailed risk register, which is regularly reviewed and updated. The risk register is reviewed monthly by the SLT, quarterly by the Finance

Committee and the Board, and undergoes an extensive review each March during the budget approval process. Risks are assessed in relation to the charity’s strategic objectives and evaluated against existing controls. Action plans are developed to minimise or eliminate risks where possible and are kept under ongoing review. A detailed review of the charity’s risk approach was last conducted in 2022/23 with the support of an external expert, including training for Trustees and the SLT.

The following risks were identified in 2024/25 as the most significant to the charity’s financial and operational sustainability:

a. Maintaining sufficient income levels: The charity closely monitors its diverse voluntary income streams through robust budget controls, targeted marketing plans, and monthly reviews of management accounts against targets.

b. Sufficient unrestricted reserves: To safeguard against income loss, unplanned expenditure, and to support strategic growth, the charity must maintain adequate unrestricted reserves. This risk was addressed through a review of the reserves policy in March 2025, resulting in an increased reserves target in line with strategic growth plans.

c. Investment market volatility: A downturn in the stock market could impact the value of the charity’s investment portfolio. This risk is mitigated through a long-term investment strategy, professional investment advice, and maintaining sufficient reserves. At 31 March 2025 over 50% of the charity’s balance sheet value is held in investments.

d. Data protection and cybersecurity: In light of GDPR and increasing cyber threats, the charity maintains strong

controls over its database, cloud storage, and cybersecurity tools. Staff receive regular training, and the Finance Committee reviews cybersecurity quarterly. The charity works closely with its external IT provider to ensure best practice, and 24-hour network monitoring was introduced in 2024/25.

e. Effective communication and outreach: Providing accurate and accessible information is essential to maintaining user trust and engagement. The charity continues to review all communications, publications, and its website to ensure they meet audience needs. A refreshed brand was launched in June 2023, followed by a new website in May 2024. A comprehensive review of health information materials concluded in June 2025.

f. Staff recruitment and retention: Talent acquisition and retention remain sector-wide challenges. The charity promotes wellbeing, sustainability, and equity through flexible, agile working arrangements and a commitment to diversity and inclusion. Since relocating to a smaller office in March 2023, the charity has expanded its recruitment reach nationally.

The Trustees continue to

regularly review the charity’s risk management framework to ensure it remains balanced and responsive to emerging risks.

Grant-making policies

The charity provides grants to support research through formal grant calls designed to attract high-quality applications. All applications undergo a peer-review process and are assessed by the Medical Research Committee and members of the Lay Research Panel. Recommendations are then made to the Board of Trustees for approval. Once awarded, grants are monitored

annually to ensure progress against agreed objectives.

Grants for equipment are administered through the charity’s subsidiary, the Joseph Patrick Trust (JPT). Applications are reviewed by the JPT Committee against established criteria before approval.

As part of our new strategy, the charity is undertaking a comprehensive review of its welfare grants programme to ensure it continues to meet the evolving needs of our community.

Reference and administrative details

The Muscular Dystrophy Group of Great Britain and Northern Ireland (Muscular Dystrophy UK) is a charitable company limited by guarantee registered with Companies House (Reg. 705357). It is also registered with the Charity Commission (Reg. 205395) and Office of the Scottish Charity Regulator (Reg.SC039445). The group also includes a trading subsidiarity, Muscular Dystrophy Group (Trading) Limited, registered with the Companies House (Reg. 893086) and unincorporated charitable subsidiary, Joseph Patrick Trust, registered with the Charity Commission (Reg. 294475).

Principal office: 32 Ufford Street, London, SE1 8QD.

Bankers: HSBC, 28 Borough High Street, London SE1 1YB and Royal Bank of Scotland, 40 Islington Road, London N1 8XJ.

Investment Managers: Rathbones London, 30 Gresham St, London EC2V 7QN.

Auditors: Moore Kingston Smith LLP, 9 Appold Street, London EC2A 2AP.

The details of the President, Patrons, Honorary Life Presidents, Vice Presidents, Trustees, Committees, SLT and advisors are set out on pages 38 to 40.

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Governance, structure and management

Governing document

experience. All appointments and resignations were approved by the Company Members with a majority vote at the AGM in October 2024.

Members

Following a review in January 2024, we now have a body of 87 charity members, who carefully monitor the charity’s progress. The charity members are volunteers drawn from the various stakeholder groups the charity represents: individuals, family members, scientists, doctors, MPs, Lords and others. Trustees are members. If you are keen on following the charity’s work and would be interested in becoming a member, please contact the charity.

The Muscular Dystrophy Group of Great Britain and Northern Ireland, operating as Muscular Dystrophy UK, is a company limited by guarantee governed by its Memorandum and Articles of Association, dated 2 September 1961 and as amended on 12 October 2019, to allow for current arrangements and charity law best practice. Muscular Dystrophy UK is registered as a charity with the Charity Commission and the Office of the Scottish Charity Regulator. Anybody over the age of 18 who supports and promotes the objectives of the charity can become a member, excluding current staff. Muscular Dystrophy UK has a wholly owned trading subsidiary, Muscular Dystrophy Group (Trading) Ltd. and not-for-profit grants giving subsidiary, Joseph Patrick Trust.

Trustee induction and training

New Trustees receive an induction pack of documents and attend briefings that cover Muscular Dystrophy UK’s operating plans, recent financial performance, and organisational structure. During the induction, and over time, they meet and form working relationships with staff. Development opportunities include ongoing training, briefings, and the annual Board Away Day.

Volunteers

Volunteers are central to our work. We rely on voluntary help in all aspects of the work of the charity. Volunteers work in the office, get involved in fundraising, provide their advice and guidance on many committees, provide support to individuals and families with muscle wasting and weakening conditions, and get involved with campaigning and media work. All these efforts help the charity achieve its aims and objectives and we would like to thank them all for their hard work and support.

Organisation

The Board of Trustees is ultimately responsible for the management of Muscular Dystrophy UK. The Board meets quarterly, and there are standing committees covering key areas of activity: for research, the Medical Research Committee (MRC) and the Lay Research Panel (LRP); for care, the Services Development Committee (SDC); for finance and fundraising, the Finance Committee; for marketing, the Content Advisory Group (CAG); for appointments, the Appointments and Remuneration Committee. A Chief Executive, with delegated authority, is appointed by and is accountable to the Trustees for managing the day-to-day operations of the charity and the delivery of operational plans.

Appointment of Trustees

Muscular Dystrophy UK currently has 13 Trustees. The selection, appointment, retirement and duties of Trustees are described in detail in the Memorandum and Articles of Association (article 29-44 et al). During the financial year 2024/25, one Trustee stepped down having completed their term, two Trustees were re-elected for a second term, and one new Trustee was elected. Their appointment was subject to a rigorous review by the Appointment and Remuneration Committee and Board of Trustees, bearing in mind the need for progressive refreshing of the Board’s skills and

Charity Governance Code

This code is a practical tool to help charities and their trustees develop high standards of governance. The Board is reminded of the code, and we continually work together on how we should apply these principles and practices during updates in the Board meetings, CEO reports and at the annual Board Away Day. In 2024/25 the

Trustees engaged in strategic workshops about the organisational purpose, vision, and values; were regularly updated on the culture of the organisation; supported on the updated risk management plans; and engaged in committees. These committees and the Board of Trustees are annually reviewed and updated to ensure they are an effective team with a balance of skills, experience, and backgrounds to make informed decisions, and to ensure that no one individual has undue power or influence.

Related parties

The Joseph Patrick Trust (JPT), an unincorporated charity, (Reg. 294475), is our welfare arm, of which Muscular Dystrophy UK is its sole corporate Trustee. Constituted on 30 April 1986, with the support of the Patrick family, it provides direct financial assistance in the form of welfare grants to individuals and families living with muscle wasting and weakening conditions, throughout the UK. The consolidated financial statements also include the trading subsidiary, Muscular Dystrophy Group (Trading) Limited (Reg. 893086). We maintain extremely close working relationships with partner charities that also assist those living with muscle wasting conditions.

Statement of Trustees’ responsibilities

the going concern basis unless it is inappropriate to presume that the charitable company will continue in operation

The Trustees, who are also the going concern basis directors of the charitable unless it is inappropriate company, are responsible for to presume that the preparing the Report of the charitable company will Trustees and the financial continue in operation statements in accordance The directors are responsible with applicable law and for keeping adequate regulations. Company law accounting records that are requires the directors to sufficient to show and explain prepare financial statements the charitable company’s for each financial year. Under transactions and disclose company law, the directors with reasonable accuracy have elected to prepare the at any time the financial financial statements in position of the charity and accordance with United group, enabling them to Kingdom Generally ensure that the financial Accepted Accounting statements comply with the Practice (United Kingdom Companies Act 2006. They Accounting Standards and are also responsible for applicable law). Under safeguarding the assets of company law, the directors the company and group and must not approve the hence for taking reasonable financial statements unless steps for the prevention and they are satisfied that they detection of fraud and give a true and fair view of other irregularities. the state of affairs of the

company and the group and the profit or loss of the group for that period.

Provision of information to auditors

So far as each of the directors is aware at the time the report is approved, there is no relevant audit information of which the company’s auditors are unaware; and the directors have taken all steps they ought to have to make themselves aware of any relevant audit information and to establish that the auditors are aware of that information. This report, incorporating the Strategic Report, is approved by the Board and signed on its behalf by:

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

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Independent auditor’s report

Opinion

We have audited the financial statements of Muscular Dystrophy Group of Great Britain and Northern Ireland (the ‘parent charitable company’) and its subsidiaries (the ‘group’) for the year ended 31 March 2025 which comprise the Consolidated Statement of Financial Activities (incorporating an Income and Expenditure Account), the Group and Parent Charitable Company Balance Sheets, the Statement of Group Cash Flows and notes to the financial statements, including 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).

In our opinion the financial statements:

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 charitable company 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.

or conditions that, individually or collectively, may cast significant doubt on the group’s and parent charitable company’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.

Other Information

The other information comprises the information included in the annual report, other than the financial statements and our auditor’s report thereon. The trustees are responsible for the other information contained in the annual report. 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.

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 course of 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 themselves.

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:

Responsibilities of the Trustees

financial statements; and As explained more fully in the trustees’ responsibilities • trustees’ annual report statement, the trustees (who (which includes the strategic are also the directors of the report) has been prepared in charitable company for the accordance with applicable purposes of company law) are legal requirements. responsible for the preparation of the financial statements and Matters on which we are for being satisfied that they give required to report by exception a true and fair view, and for such In the light of the knowledge internal control as the trustees and understanding of the group determine is necessary to and parent charitable company enable the preparation of and their environment obtained financial statements that in the course of the audit, we are free from material have not identified material misstatement, whether misstatements in the trustees’ due to fraud or error.

In the light of the knowledge and understanding of the group and parent charitable company and their environment obtained in the course of the audit, we have not identified material misstatements in the trustees’ annual report (which includes the strategic report).

In preparing the financial statements, the trustees are responsible for assessing the group and 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

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

accounting unless the trustees either intend to liquidate the group or 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

We have been appointed as auditor under Section 44(1)(c) of the Charities and Trustee Investment (Scotland) Act 2005 and under the Companies Act 2006 and report to you in accordance with regulations made under those Acts.

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 aggregate, they could reasonably be expected to influence the economic decisions of users taken on the basis of these financial statements.

As part of an audit in accordance with ISAs (UK) we exercise professional judgement and maintain professional scepticism throughout the audit.

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We also:

the financial statements or, if such disclosures are inadequate, to modify our opinion. Our conclusions are based on the audit evidence obtained up to the date of our auditor’s report. However, future events or conditions may cause the group or parent charitable company to cease to continue as a going concern.

We communicate with those charged with governance regarding, among other matters, the planned scope and timing of the audit and significant audit findings, including any significant deficiencies in internal control that we identify during our audit.

Explanation as to what extent the audit was considered capable of detecting irregularities, including fraud.

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.

The objectives of our audit in respect of fraud, are to identify and assess the risks of material misstatement of the financial statements due to fraud; to obtain sufficient appropriate audit evidence regarding the assessed risks of material misstatement due to fraud, through designing and implementing appropriate responses to those assessed risks; and to respond appropriately to instances of fraud or suspected fraud identified during the audit. However, the primary responsibility for the prevention and detection of fraud rests with both management and those charged with governance of the charitable company.

Our approach was as follows:

• We obtained an

understanding of the legal and regulatory requirements applicable to the charitable company and considered that the most significant are the Companies Act 2006, the Charities and Trustee Investment (Scotland) Act 2005 (as amended), regulations 6 and 8 of the Charities Accounts (Scotland) Regulations 2006 (as amended), the Charity SORP, and UK financial reporting standards as issued by the Financial Reporting Council

• We obtained an

understanding of how the charitable company complies with these requirements by discussions with management and those charged with governance.

There are inherent limitations in the audit procedures described above. We are less likely to become aware of instances of non-compliance with laws and regulations that are not closely related to events and transactions reflected in the financial statements. Also, the risk of not detecting a material misstatement due to fraud is higher than the risk of not detecting one resulting from error, as fraud may involve deliberate concealment by, for example, forgery or intentional misrepresentations, or through collusion.

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 and to the charitable company’s trustees, as a body, in accordance with Section 44(1) (c) of the Charities and Trustee Investment (Scotland) Act 2005. Our audit work has been undertaken so that we might state to the charitable company’s members and trustees those matters which we are required to state to them in an auditor’s report addressed to them and for no other purpose. To the fullest extent permitted by law, we do not accept or assume responsibility to any party other than the charitable company and charitable company’s members as a body, and the charity’s trustees, as a body, for our audit work, for this report, or for the opinions we have formed.

Andrew Stickland

Senior Statutory Auditor

for and on behalf of Moore Kingston Smith LLP, Statutory Auditor

9 Appold Street, London EC2A 2AP

Moore Kingston Smith LLP is eligible to act as auditor in terms of Section 1212 of the Companies Act 2006.

Date: 27 October 2025

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Financial statements and notes

Consolidated statement of financial activities (Incorporating an income and expenditure account)

For the year ended 31 March 2025

----- Start of picture text -----
Notes Unrestricted Restricted and Total Unrestricted Restricted and Total
funds endowment 2025 funds endowment 2024
£000 funds £000 £000 funds £000
£000 £000
Income
Income from
charitable activities
Donations, gifts 2 3,933 548 4,482 3,340 1,131 4,471
and grants
Government grants 2 - 15 15 - 847 847
Legacies 2 2,466 128 2,595 2,219 701 2,920
Income from other
11 194 - 194 67 - 67
trading activities
Investment income 2, 10 554 - 554 340 - 340
Other income 2 56 16 72 5 858 863
Total income 7,205 707 7,912 5,971 3,537 9,508
Expenditure
Expenditure on 3 2,754 336 3,090 2,135 347 2,482
raising funds
Costs from other
trading activities 3 132 - 132 114 - 114
2,887 336 3,222 2,249 347 2,596
Charitable activities
Medical research 3, 5 1,785 562 2,346 523 1,653 2,176
Access to specialist 3 1,339 (57) 1,282 1,180 53 1,233
care and support
Independent living 3 1,070 2,171 3,241 813 1,224 2,037
Total – charitable
4,194 2,675 6,869 2,516 2,930 5,446
activities
Total expenditure 7,080 3,011 10,091 4,765 3,277 8,042
Net gain/(loss) on 9 112 (4) 109 410 32 442
investment assets
Transfer between funds - - - - - -
Net movement
237 (2,308) (2,071) 1,616 292 1,908
in funds
Reconciliation of funds
Total funds
15 8,564 5,257 13,821 6,948 4,965 11,913
brought forward
Total funds
15 8,801 2,949 11,751 8,564 5,257 13,821
carried forward
----- End of picture text -----

There are no recognised gains or losses other than those disclosed above. All results are derived from continuing activities. The accompanying notes on pages 56 to 67 form an integral part of the financial statements.

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Balance sheets

As at 31 March 2025

Statement of group cashflows

Year ended 31 March 2025

company registration number: 205395

----- Start of picture text -----
Notes Group Group Charity Charity
2025 2024 2025 2024
£000 £000 £000 £000
Fixed assets
Tangible assets 8 274 370 274 370
Investments 9 5,924 6,013 5,796 5,767
6,197 6,383 6,070 6,137
Total fixed assets
Current assets
Stock 12 17 14 - -
Debtors 13 1,787 2,458 1,803 2,517
Short term investments 1,000 1,000 1,000 1,000
Cash at Bank 7,194 7,608 7,077 7,494
Total current assets 9,998 11,080 9,880 11,011
Creditors falling due within one year 14 (4,444) (3,642) (4,294) (3,417)
Net current assets 5,553 7,438 5,585 7,594
Total assets less current liabilities 11,751 13,821 11,655 13,731
Net assets 11,751 13,821 11,655 13,731
The funds of the Charity
Unrestricted
- Designated 15 4,801 2,876 4,801 2,876
- General 15 4,000 5,688 3,926 5,598
8,801 8,564 8,727 8,474
Restricted 15 2,534 4,838 2,512 4,838
Endowment 15 415 419 415 419
Total charity funds 11,751 13,821 11,655 13,731
----- End of picture text -----

The Statement of Financial Activities for the year ended 31 March 2025 for the parent charitable company only was a deficit of £2,076K (2024: surplus of £2,040K).

The accompanying notes on pages 56 to 67 form an integral part of the financial statements.

Approved and authorised for issue by the Board of Trustees on 17 October 2025 and signed on its behalf by:

Professor Michael Hanna

Joseph Gordon Treasurer 17 October 2025

Chairman

17 October 2025

----- Start of picture text -----
2025 2024
£000 £000
Net cash inflow/(outflow) from operating activities (note a) (1,129) (182)
Net cash flow from investing activities
Dividends from investments 554 407
Purchase of tangible fixed assets (37) (86)
Proceeds of sale of Investments 2,214 976
Purchase of Investment (2,016) (2,148)
Net cash provided by investing activities 715 (851)
Increase/(decrease) in cash and cash equivalents in the year (414) (1,033)
Increase/(decrease) in cash and cash equivalents in the year (note b) (414) (1,033)
Cash and cash equivalents at the beginning of the year 7,608 8,641
Cash and cash equivalents at the end of the year 7,194 7,608
Notes to cash flow statement
(a) Reconciliation of net movement in funds to net cash flow
from operating activities:
Net movement in funds (2,071) 1,908
Dividends from investments (554) (407)
Investment (gains) / losses (109) (442)
Depreciation 109 117
Loss on assets disposal 25 -
Decrease / (Increase) in debtors / stock 668 (958)
Increase / (Decrease) in all creditors 802 (400)
Net cash provided by/(used in) operating activities (1,129) (182)
01-Apr-24 Cashflows 31-Mar-25
£000 £000 £000
(b) Analysis of changes in net cash funds:
Cash and cash equivalents 7,608 (414) 7,194
Total cash and cash equivalents 7,608 (414) 7,194
----- End of picture text -----

The accompanying notes on pages 56 to 67 form an integral part of the financial statements.

The accompanying notes on pages 56 to 67 form an integral part of the financial statements.

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Notes to the financial statements

For the year ended 31 March 2025

Policies

1. Accounting policies

Accounting convention

The financial statements have been prepared in accordance with Accounting and Reporting by Charities: Statement of Recommended Practice for Charities (SORP 2015) (Second Edition, effective 1 January 2019) applicable to charities preparing accounts in accordance with the Financial Reporting Standard applicable in the UK and Republic of Ireland (FRS102) and the Companies Act 2006. The financial statements have been prepared under the historical cost convention unless otherwise stated in the relevant accounting policy note(s). Muscular Dystrophy UK meets the definition of a public benefit entity under FRS102.

Consolidation has been done

on a line-by-line basis, with all inter-company transactions eliminated. The accounting dates and policies are the same.

Income

Income is recognised in the SOFA when the effect of the transaction results in an increase in the charity’s assets. This will be dependent on three factors:

i. Entitlement – when Muscular

Dystrophy UK has control over the rights to the resource, enabling it to receive the economic benefit.

The principal accounting policies adopted in the preparation of the financial statements are set out below.

ii. Probability – when it is probable, more likely than not that the economic benefit will be received.

Going concern accounting policies

iii. Measurement – when the monetary value can be measured with sufficient reliability.

The charitable company’s level of free reserves available at the year end, were considered adequate resources to continue in operational existence for the foreseeable future. The budgets and cash flows for 2025/26 were reviewed in October 2025 and the Trustees have considered cash forecasts covering the twelve month period until October 2026. Accordingly, the financial statements have been prepared on a going concern basis and the trustees do not anticipate any material uncertainties.

Income received for a specific purpose is treated as restricted funds. Where income is received subject to donorimposed conditions that specify a future time period in which the expenditure should take place, such income is deferred and recognised as a liability. It is released as income in the accounting period in which Muscular Dystrophy UK is allowed to expend the resource.

Basis of consolidation

Subsidiary undertakings are fully consolidated and hence these financial statements are referred to as ‘consolidated financial statements. Non-autonomous branches are treated as part of the parent charity and are referred to as ‘charity’ financial statements. A separate Statement of Financial Activities (SOFA) for the parent charity is not presented because Muscular Dystrophy UK has taken advantage of the exemption afforded by section 408 of Companies Act 2006. The subsidiary undertakings included in these consolidated accounts include:

Receipt of a legacy, in whole or in part, is only considered probable when the amount can be measured reliably through estate accounts (or cash receipt) and the charity has been notified of the executor’s intention to make a distribution. Where legacies have been notified to the charity or the charity is aware of the granting of probate, and the criteria for income recognition have not been met, then the legacy is not recognised in the accounts.

Services in kind are valued at the lower of their market value and • Muscular Dystrophy Group (Trading) equivalent market cost were these to Limited (registered company be purchased directly by the charity. number 00893086). The Trustees consider that all services in kind received in 2024/25 do not meet recognition criteria outlined in module

6 of the charity SORP 2019. Therefore, no estimates for these services were included in this set of accounts.

Expenditure

All expenditure is recognised on an accruals basis and includes irrecoverable VAT where appropriate. Grants awarded are recognised as a liability when Muscular Dystrophy UK is under a legal or constructive obligation to a third party. Expenditure on raising funds includes all expenditure incurred in pursuance of Muscular Dystrophy UK’s fundraising activities.

Charitable expenditure includes all expenditure incurred in pursuance of Muscular Dystrophy UK’s objectives. The costs of these activities are divided between grants and other direct costs. Support costs including governance costs have been allocated to each activity on the basis of expenditure incurred.

Governance costs include those

costs associated with meeting the constitutional and statutory requirements of the charity and include audit fees and costs linked to the strategic management of the charity.

Muscular Dystrophy UK awards three types of grants:

  1. Grants to fund medical research.

  2. Grants for the installation of Changing Places toilets.

  3. Grants to specific beneficiaries to enable them to purchase equipment to alleviate their muscle wasting and weakening condition, and other small welfare grants dispensed to individual beneficiaries.

Taxation

Muscular Dystrophy Group of Great Britain and Northern Ireland and the Joseph Patrick Trust are registered charities with the meaning of para 1 schedule 6 Finance Act 2010. Accordingly, they are exempt from taxation in respect of income or capital gains within categories covered by Chapter 3 of Part 11 of the Corporation Tax Act 2010 or section 256 of the Taxation of Chargeable Gains Act 1992, to the extent that such income or gains

1. Accounting policies (Cont.)

are applied exclusively to charitable purposes. No tax charge arose in the period.

Muscular Dystrophy Group (Trading) Limited donates by way of Gift Aid all taxable profits to the parent charity.

Listed investments

Listed investments are shown at the bid-market value ruling at the date of the Balance Sheet and after taking into account any subsequent impairment in value. Muscular Dystrophy UK has full discretion in its investment policy.

The Statement of Financial Activities includes the aggregate of realised and unrealised gains and losses during the year.

Unlisted investments

Unlisted investments are shown at cost unless there is reason to believe that there has been a significant reduction in their value.

Financial instruments

Basic financial instruments are initially recognised at transaction value and subsequently measured at amortised cost with the exception of investments which are held at fair value. Financial assets held at amortised cost comprise cash at bank and in hand, together with trade and other debtors. A specific provision is made for debts for which recoverability is in doubt. Financial liabilities held at amortised cost comprise all creditors except social security and other taxes.

Intangible and tangible fixed assets and depreciation

Items or projects with a value exceeding £500, and which have a life exceeding one year, are capitalised. Improvements to leasehold property are depreciated over the full length of the lease. Depreciation is provided on all other tangible fixed assets on a straight-line basis to write off the cost as follows:

Leasehold premises: over length of lease

Motor Vehicles: over three years All other assets: over four years.

Accounting estimates and areas of significant judgment

Operating leases

The charity provides for operating leases on property on an actual cost basis. Rent-free periods on property are apportioned over the life of the lease. Any rent-free period is to offset the additional costs incurred by moving into new premises and reflects the inducement offered in that period by the landlord to let the property.

In preparing the financial statements, Trustees are required to make estimates, judgements and assumptions that affect the application of the charity’s accounting policies and the reported assets, liabilities, income and expenditure and the disclosures made in the financial statements. Estimates and judgements are continually evaluated and are based on historical experience and other factors, including expectations of future events that are believed to be reasonable under the circumstances. Actual results may differ from these estimates.

Debtors

Trade and other debtors are recognised at the settlement amount due after any trade discount offered. Prepayments are valued at the amount prepaid net of any trade discounts due.

Judgement and estimates have been applied in the accounts in the following key areas:

Cash at bank and in hand

Cash at bank and cash in hand includes cash and short term highly • Estimating the useful economic liquid investments with a short maturity life of tangible fixed assets of three months or less from the date of acquisition or opening of the deposit • Estimating the probability of or similar account or matures within the receipt of legacy income three months of the date of the and the amount to be received balance sheet.

Creditors and provisions

Creditors and provisions are recognised where the charity has a present obligation resulting from a past event that will probably result in the transfer of funds to a third party and the amount due to settle the obligation can be measured or estimated reliably. Creditors and provisions are normally recognised at their settlement amount after allowing for any trade discounts due.

Stock

Stock is included at the lower of cost or net realisable value. Donated items of stock are recognised at fair value, which is the amount the charity would have been willing to pay for the items on the open market.

Fund accounting policies

Unrestricted funds are funds received and applied to achieve the general objectives of the MDUK.

Employee benefits

Short term benefits including holiday pay are recognised as an expense in the period in which the service is received. Employee termination benefits are accounted for on an accrual basis and in line with FRS 102.

Designated funds are unrestricted funds earmarked by the Trustees for particular purposes.

Endowment funds are represented by capital assets held as investments which generate income which in turn is applied to specific objectives of the MDUK as laid down by the donor.

Pensions

Muscular Dystrophy UK offers defined contributions to employees’ pension arrangements. The amount charged to the SOFA in respect of pensions costs is the contributions payable within the year. Differences between contributions payable and contributions actually paid are shown as accruals in the Balance Sheet.

Restricted funds are to be used for specified purposes as laid down by the donor. Expenditure which meets these criteria is identified to the fund, together with a fair allocation of support costs where applicable.

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Notes to the financial statements

For the year ended 31 March 2025

2. Income

----- Start of picture text -----
Unrestricted Restricted Total Unrestricted Restricted Total
funds funds 2025 funds funds 2024
£000 £000 £000 £000 £000 £000
Events and promotions 1,926 24 1,951 1,582 144 1,726
Direct marketing 790 12 802 810 14 824
Major donors and corporate 564 114 678 414 692 1,106
Trusts 28 164 193 50 844 894
Regional development 625 248 873 484 284 768
Legacies 2,466 128 2,595 2,219 701 2,920
Other income 805 16 821 412 858 1,270
Total income 7,205 707 7,912 5,971 3,537 9,508
----- End of picture text -----*

* Of this income £15k net comes from Government Grants (2024: £847k). The government grants included a refund of £10k (2024 payment of £740k) to the Department of Transport and £25k (2024: £106k) from Ministry of Housing, Communities and Local Government included in Other income figure.

3. Expenditure

----- Start of picture text -----
Grants Other Support Total
£000 £000 Costs 2025
£000 £000
----- End of picture text -----

Raising funds
Expenditure on raising funds
Costs from other Trading Activities
Total
Charitable expenditure
Access to care and independent living
Access to care
Independent living
Total
Pursuit of Knowledge
Medical research
Total charitable expenditure
Total expenditure		 -
2,855
235
3,090
-
123
10
132
-
2,977
245
3,222
-
1,101
181
1,282
1,887
896
458
3,241
1,887
1,997
639
4,523
1,613
402
331
2,346
3,500
2,399
970
6,869
3,500
5,377
1,215
10,091

3. Expenditure (Cont.)

----- Start of picture text -----
2024 Comparatives Grants Other Support Total
£000 £000 Costs 2024
£000 £000
Raising funds
Expenditure on raising funds - 2,329 153 2,482
Costs from other trading activities - 109 5 114
Total - 2,438 158 2,596
Charitable expenditure
Access to care and independent living
Access to care - 1,085 148 1,233
Independent living 1,018 774 245 2,037
Total 1,018 1,859 393 3,270
Pursuit of knowledge
Medical research 1,578 337 261 2,176
Total charitable expenditure 2,596 2,196 654 5,446
Total expenditure 2,596 4,634 812 8,042
‘Direct costs’ include all costs incurred in delivering the relevant activity.
‘Support costs’ comprise of the following:
2025 2024
£000 £000
Chief Executive and Human Resources 194 134
Finance and insurance 430 263
Office costs 337 220
Information Technology 213 160
Governance 41 36
Total 1,215 813
----- End of picture text -----

These costs have been allocated across the activities on the basis of expenditure incurred for each of the activities.

4. Staff costs (Group and Parent Charity)

----- Start of picture text -----
2025 2024
£000 £000
Remuneration of staff
Wages and salaries 2,659 2,386
Social security costs 278 239
Pensions 154 127
Total 3,090 2,752
----- End of picture text -----

There were three redundancies made in the year (2024: No redundancies were made in the year). The cost of the redundancy payments was £2.5k (2024: £nil). The monthly average number of employees during the period was 73 (2024: 70), of whom there were the following higher paid employees as detailed below.

Details of the Key Management Personnel, which consists of the Senior Management Team, can be found on page 38. Their total aggregate employment benefits were £552k (2024: £469k).

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4. Staff costs (Group and Parent Charity) (Cont.)

----- Start of picture text -----
2025 2024
No. No.
Earned between the ranges
£60,000 to £70,000 4 1
£70,001 to £80,000 3 1
£80,001 to £90,000 1 1
£100,001 to £110,000
£110,001 to £120,000 1 1
Number of staff by activity
Direct charitable expenditure 25 25
Fundraising and publicity 40 38
Management and administration 8 7
Total 73 70
----- End of picture text -----

Pension schemes

There was £21k outstanding pension contribution (2024: £nil) at the Balance Sheet date.

5. Grant expenditure

----- Start of picture text -----
Research Welfare Total Total
grants grants 2025 2024
£000 £000 £000 £000
Grants awarded in the year 1,708 1,904 3,612 2,874
Grants cancelled in the year (95) (17) (112) (279)
Total 1,613 1,887 3,500 2,595
----- End of picture text -----

2024 comparatives Research
grants
£000		 Welfare
grants
£000		 Total
2024
£000
Grants awarded in the year
Grants cancelled in the year
Total		 1,785
1,089
2,874
(208)
(71)
(279)
1,577
1,018
2,595

With the exception of some welfare grants that are paid to individuals, all grants are paid to institutions. A list of grants to institutions is available from the registered office. The Welfare grants include Changing Places grants.

Two institutions were in receipt of a total of three material research grant awards exceeding £80k in 2024/25. Two of these went to the Unversity of Cambridge (one strategic grant of £188k and one project grant £87k) and one to University College London (strategic grant £352k). Grant expenditure includes a repayment of £273k (2024: £nil) to the Department for Transport in respect of unutilised funds following the closure of a project. In addition, £99k was transferred during the year from the A Road Project to the Rail Network Project.

At the balance sheet date, the charity had conditional grant commitments that had not been accrued in the accounts, as all the criteria relating to payment in subsequent years had not been met of £2,565k (2024: £1954k).

5. Grant expenditure (Cont.)

Reconciliation of grant funding commitments:

2025
£000		 2024
£000
Carrying amount at start of year
Additions
Amounts charged and cancelled in year
Carrying amount at end of year		 3,113
3,003
3,612
2,874
(3,513)
(2,764)
3,212
3,113

6. Operating lease commitments

Muscular Dystrophy UK is committed to the following minimum lease commitments under a non-cancellable operating lease on its headquarters and office equipment.

----- Start of picture text -----
2025 2024
£000 £000
Expiring up to one year 148 90
Expiring between one and five years 440 522
Expiring after more than five years - 540
----- End of picture text -----

7. Net income

Net Income is stated after charging

----- Start of picture text -----
2025 2024
£000 £000
Auditor’s remuneration 37 32
Auditor’s remuneration - non audit services 3 4
Depreciation 109 117
Operating lease rentals 128 129
----- End of picture text -----

8. Tangible fixed assets

----- Start of picture text -----
Group Leasehold Computer Motor Other Other Total
premises equipment cars assets equipment £000
£000 £000 £000 £000 £000
----- End of picture text -----

Cost at 1 Apr 2024
Additions
At 31 Mar 2025
Depreciation 1 Apr 2024
Disposal
Provided for year
At 31 Mar 2025
Net Book Value
At 31 Mar 2025
At 31 Mar 2024		 126
500
16
15
31
688
35
-
-
1
37
117
359
9
15
37
537
11
282
16
-
9
318
-
(157)
(8)
-
-
(164)
12
89
-
-
9
109
23
213
9
-
19
264
94
146
-
15
19
274
115
218
0
15
21
370

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8. Tangible fixed assets (Cont.)

----- Start of picture text -----
Parent Charity Leasehold Computer Motor Other Other Total
premises equipment cars assets equipment £000
£000 £000 £000 £000 £000
----- End of picture text -----

Cost at 1 Apr 2024
Additions
Disposal
At 31 Mar 2025
Depreciation 1 Apr 2024
Disposal
Provided for year
At 31 Mar 2025
Net Book Value
At 31 Mar 2025
At 31 Mar 2024		 126
497
16
15
31
685
35
-
-
1
37
(9)
(175)
(8)
-
5
(187)
117
357
9
15
37
535
11
279
16
-
9
315
-
(156)
(8)
-
-
(164)
12
89
-
-
9
109
23
211
9
-
19
261
94
146
-
15
19
274
115
218
0
15
22
370

All tangible fixed assets are used in the promotion of Muscular Dystrophy UK’s work; none are held for investment. Included in Other Assets are three portraits especially commissioned by the charity; they are held at a cost of £15k. In the opinion of the Trustees, they are worth not less than this valuation and as such no depreciation is charged.

9. Investments

----- Start of picture text -----
Group Group Charity Charity
2025 2024 2025 2024
£000 £000 £000 £000
Market value at beginning of year 6,012 5,399 5,765 5,169
Acquisitions 2,016 1,148 1,757 1,070
Sales proceeds (2,214) (976) (1,826) (896)
Total 5,815 5,571 5,696 5,343
Gain/(loss) on investment 109 442 100 424
Market value at end of year 5,924 6,013 5,796 5,767
Historical cost at end of year 5,020 5,409 4,894 5,165
----- End of picture text -----

Spread of investments

The investments of Muscular Dystrophy UK are held as follows:

----- Start of picture text -----
Group Group Charity Charity
2025 2024 2025 2024
£000 £000 £000 £000
Investments listed on a recognised
Stock Exchange and Unit Trusts
UK and overseas equities 4,549 4,665 4,549 4,477
UK and overseas fixed interest 775 757 653 725
Property and Infrastructure funds 569 219 564 210
Hedge funds - 310 - 293
Total 5,893 5,951 5,767 5,705
Cash on deposit awaiting investment 30 - 29 -
Unlisted equities - 62 - 62
Total 5,924 6,013 5,796 5,767
----- End of picture text -----

10. Income from investments

----- Start of picture text -----
Group Group Charity Charity
2025 2024 2025 2024
£000 £000 £000 £000
UK Equities, UK fixed interest and other 118 46 113 45
Short term deposit and bank interest 436 294 435 286
Total 554 340 548 331
----- End of picture text -----

11. Investments in subsidiary undertakings

The accounts of Muscular Dystrophy UK (i.e. ‘charity’ accounts) incorporate the results of the following entities on a line-by-line basis:

Their net assets and results for the year ended 31 March 2025 are summarised below:

----- Start of picture text -----
Muscular Dystrophy Joseph Patrick Trust
Group (Trading) Ltd £000
£000
----- End of picture text -----

Fixed assets
Current assets
Current liabilities
Total net assets
Represented by:
Total funds
Total income
Total expenditure
Investment gains/losses and other B/S movements
Surplus for the year
Country of registration
Number of fully paid £1 ordinary shares
Voting rights owned by Muscular Dystrophy UK		 -
128
118
43
(100)
(93)
18
77
18
77
194
160
(132)
(225)
-
8
62
(57)
England
England
100
-
100%
100%

12. Stock

The stock held in Muscular Dystrophy Group (Trading) Ltd represents new goods available for sale valued at £17k (2024 : £14k).

13. Debtors

----- Start of picture text -----
Group Group Charity Charity
2025 2024 2025 2024
£000 £000 £000 £000
Trade debtors 23 32 - -
Amount due from subsidiary undertakings - - 42 97
Prepayments and accrued income 1,764 2,424 1,760 2,418
Other debtors - 2 - 2
Total 1,787 2,458 1,803 2,517
----- End of picture text -----

Investment management costs for the year were £49k (2024: £27k).

During the year, the sale of an unlisted investment resulted in a realised gain of £145k included in the gain in the Statement of Financial Activities.

All amounts are due within one year, and all intra group balances are unsecured and do not bear interest.

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14. Creditors falling due within one year

----- Start of picture text -----
Group Group Charity Charity
2025 2024 2025 2024
£000 £000 £000 £000
Accruals for grant commitments 3,212 3,113 3,027 2,939
Accruals and deferred Income 478 350 421 344
Taxation and social security 64 6 64 -
Amount due from/to subsidiary undertakings - - 94 -
Trade creditors 670 120 667 115
Other creditors 21 53 21 19
Total 4,444 3,642 4,294 3,417
----- End of picture text -----

15. Funds

----- Start of picture text -----
April Income Expenditure Movement Investment March
2024 £000 £000 between gains 2025
£000 funds £000 £000
£000
----- End of picture text -----

Endowment fund
Orchid Ball
Restricted funds
Provision of care
City Bridge Trust /
Work experience
Scotland
Psychological support
Volunteering
Joseph Patrick Trust -
Assistive technology
Changing Places
The Garfield Weston
CCS Fund
SMA screening
Chelsea Flower Show
Other care
Research
The Patrick Research Fund
Congenital LMNA MD
Q Trust
FSHD Research
Duchenne Research
Ullrich Research
Nemaline Research
Congenital MD
Becker Research Fund
SMA Research
Limb Girdle Research
Other research
Total restricted funds		 419
-
-
-
(4)
415
-
5
(5)
-
-
-
603
94
(93)
-
-
604
8
2
(10)
-
-
-
-
11
(11)
-
-
-
43
1
(21)
-
-
22
1,885
17
(1,902)
-
-
-
-
2
(2)
-
-
-
26
-
(23)
-
-
3
284
44
(328)
-
-
(-)
2
69
(54)
-
-
17
100
-
(100)
-
-
(-)
92
12
(26)
-
-
78
97
5
-
-
-
102
96
52
(75)
-
-
73
120
86
-
-
-
206
142
48
(75)
-
-
116
282
26
-
-
-
308
284
-
(63)
-
-
221
75
18
-
-
-
93
7
30
(12)
-
-
25
165
77
(75)
-
-
168
526
108
(135)
-
-
498
4,838
707
(3,011)
-
-
2,534

15. Funds (Cont.)

April
2024
£000		 Income
£000		 Expenditure
£000		 Movement
between
funds
£000		 Investment
gains
£000		 March
2025
£000
Designated funds
IT Investment fund
Research
Fundraising
Data team
Tangible assets for charity use
Strategic investment fund
Total designated funds
General fund
Strategic investment fund
Total general fund
Total unrestricted funds
Total funds		 36
-
-
-
36
2,150
-
(540)
-
-
1,610
170
-
(170)
-
-
-
150
-
(53)
-
-
97
370
201
(297)
-
-
274
-
-
-
2,784
-
2,784
2,876
201
(1,060)
2,784
-
4,801
5,688
7,004
(6,020)
(2,784)
112
4,000
-
-
-
-
-
(2,784)
5,688
7,004
(6,020)
(2,784)
112
4,000
8,564
7,205
(7,080)
-
112
8,801
13,821
7,912
(10,091)
-
109
11,751
2024 comparatives April
2023
£000		 Income
£000		 Expenditure
£000		 Movement
between
funds
£000		 Investment
gains
£000		 March
2024
£000
Endowment fund
Orchid Ball
Restricted funds
Provision of care
City Bridge Trust /
Work experience
Scotland
Psychological support
Volunteering
Joseph Patrick Trust -
Assistive technology
Changing Places
The Garfeld Weston
CCS Fund
SMA screening
Chelsea Flower Show
Other care
Research
The Patrick Research Fund
Congenital LMNA MD
Q Trust
FSHD Research
Duchenne Research
Ullrich Research
Nemaline Research
Congenital MD
Becker Research Fund
SMA Research
Limb Girdle Research
Other research
Total restricted funds		 387
-
-
-
32
419
4
-
(4)
-
-
-
-
634
(31)
-
-
603
29
-
(20)
-
-
9
-
21
(21)
-
-
-
49
-
(6)
-
-
43
2,211
868
(1,194)
-
-
1,885
117
-
(117)
-
-
-
-
95
(69)
-
-
26
-
605
(321)
-
-
284
2
17
(16)
-
-
3
100
-
-
-
-
100
59
33
2
-
-
94
21
85
(9)
-
-
97
77
35
(16)
-
-
96
167
240
(287)
-
-
120
116
63
(38)
-
-
141
371
8
(97)
-
-
282
465
1
(182)
-
-
284
150
6
(82)
-
-
74
14
23
(30)
-
-
7
47
118
-
-
-
165
579
685
(739)
525
4,578
3,537
(3,277)
-
-
4,838

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15. Funds (Cont.)

----- Start of picture text -----
2024 comparatives April Income Expenditure Movement Investment March
2023 £000 £000 between gains 2024
£000 funds £000 £000
£000
----- End of picture text -----

£000
funds
£000

£000
£000
Designated funds
IT Investment fund
Research
Fundraising
Data team
Tangible assets for charity use
Total designated funds
General fund
Total unrestricted funds
Total funds		 36
-
-
-
-
36
-
-
-
2,150
-
2,150
-
-
-
170
-
170
-
-
-
150
-
150
401
86
(117)
-
-
370
437
86
(117)
2,470
-
2,876
6,511
5,885
(4,648)
(2,470)
410
5,688
6,948
5,971
(4,765)
-
410
8,564
11,913
9,508
(8,042)
-
442
13,821

Endowment fund

by the Garfield Weston Trust to improve the reach of our support and increase our policy capacity to support NHS neuromuscular services.

The Orchid Ball Fund is an endowed fund, the income from which (shown separately) is restricted in the first instance to research and welfare in Scotland. Any unused income in a financial period is then directed to funding research.

Other Care - this includes funding for our Muscle Group activity and work to connect families from underrepresented backgrounds affected by muscle wasting conditions with each other.

Restricted Fund

City Bridge Trust / Work experience - this is funding received from the City Bridge Trust to support young disabled people in the London area to access work experience and develop their employability skills.

The Patrick Research Fund - this is a donation from the Patrick family. It is used to support research activities relating to Duchenne muscular dystrophy.

Congenital Muscular Dystrophy - this is used to support research related to the condition congenital muscular dystrophy conditions.

Scotland - this is used for activities in Scotland.

Psychological Support - this is used to support our Mental Health Matters work, identifying how MDUK can best improve the mental health and wellbeing support available for people affected by muscle wasting conditions..

Oxford Neuromuscular Centre - this is used to support the funding of the MDUK Oxford Neuromuscular Centre - much of the fund has come from the Q Trust.

Volunteering - this is funding to support our work to identify a more strategic and sustainable approach to working with volunteers to help support our community.

Q Trust Fellowship - this funding comes from the Q Trust - the restriction is reviewed annually by the Q Trusts representatives in line with their wishes and projects of interest.

The Joseph Patrick Trust is a restricted trust within Muscular Dystrophy UK as explained in Note 11. Its assets are restricted to ‘provide welfare, relief and support to those living with muscle wasting conditions.’

F SHD Research - this is used to support research related to the condition FSHD (facioscapulohumeral muscular dystrophy).

MDUK currently holds seven restricted funds related to our role as co-chair of the Changing Places consortium. These seven funds are for:

Duchenne MD Research - this is used to support research related to the condition Duchenne muscular dystrophy.

Ullrich MD Research - this is used to support research related to the condition Ullrich congenital muscular dystrophy and other collagen-VI-related muscular dystrophies.

Nemaline Myopathy Research - this is used to support research related to the condition nemaline myopathy. A significant proportion of these funds came via the MAP Nemaline family fund.

Congenital LMNA MD - this is used to support research related to the condition LMNA congenital muscular dystrophy.

Becker Research Fund - this is used to support research related to the condition Becker muscular dystrophy.

SMA Research - this is used to support research related to the condition spinal muscular atrophy.

Limb Girdle MD Research - this is used to support research related into limb girdle muscular dystrophies.

Other research - this is used to support research grants for which there are no condition restrictions.

Designated Fund represents IT investment in CRM and Cloud migration projects and two strategic programmes.

The Garfield Weston CCS Fund - two year project funded

Unrestricted funds

The designation of balances is as follows:

Muscular Dystrophy UK’s reserves policy is reviewed regularly to ensure that the charity has sufficient cash and other reserves to meet its present and future commitments in an orderly and sustainable manner.

Represented by: 2025 Fixed assets
£000		 Investments
£000		 Net current assets
£000		 Total
£000
Endowment funds
Restricted funds
Designated funds
Unrestricted funds
Total funds		 -
415
-
415
-
-
2,534
2,534
274
1,508
3,019
4,801
4,000
-
4,000
274
5,924
5,553
11,751
Represented by: 2024 Fixed assets
£000		 Investments
£000		 Net current assets
£000		 Total
£000
Endowment funds
Restricted funds
Designated funds
Unrestricted funds
Total funds		 -
419
-
419
-
-
4,838
4,838
370
-
2,506
2,876
-
5,594
94
5,688
370
6,013
7,438
13,821

16. Legacies

The charity is entitled to a share in a number of estates which it monitors closely. The following sums have not been reflected in these financial statements in accordance with the accounting policies set out in Note 1. The potential values of these estates to the charity at the balance sheet date are as follows:

----- Start of picture text -----
2025 2024
£000 £000
Residuary 22 341
Reversionary 167 252
All sums are due to Muscular Dystrophy UK. 189 593
----- End of picture text -----

17. Status of charity

Muscular Dystrophy Group of Great Britain and Northern Ireland, operating as Muscular Dystrophy UK, is a registered charity and a company limited by guarantee. In the event of a winding up, Members are required to contribute an amount not exceeding £1. By virtue of s.30 of the Companies Act 2006, the charity does not use ‘limited’ in its name.

18. Related party transactions

During the year Trustees of Muscular Dystrophy UK made donations to the charity and received reimbursement of their expenses incurred in travelling to attend Muscular Dystrophy UK’s business, as per below. The charity also contracted with Chimera, to provide services to the value of £29k (2024: £25k) for the Microscope Ball. Chimera is owned by the husband of the charity’s Director of Development. Emma Parry-Jones had no involvement in the Trustees decision to use this supplier:

2025
£000		 2024
£000
Donations
17
5
Expenses
2
5
No Trustee received any remuneration during the year (2024: £nil).
There were no other related parties transactions.

Muscular Dystrophy Group of Great Britain and Northern Ireland. Registered charity in England and Wales (205395) and Scotland (SC039445) and a company limited by guarantee without share capital registered with Companies House (705357). Registered office address: 32 Ufford Street, London, England, SE1 8QD