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2025-09-30-accounts

Trustees' Annual Report for the period

Period start date Period end date 01 10 2024 30 09 2025 From To

Section A Reference and administration details

Charity name

INVEST in ME RESEARCH

Other names charity is known by IiMER InMER IiME RESIME Invest in ME

Registered charity number (if any) 11153730

Charity's principal address

PO Box 561 Eastleigh Hampshire Postcode SO50 0GQ

Names of the charity trustees who manage the charity

1
2
3
4
5
6
7
8
9
10
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14
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18
19
20
Trustee name Office (if any) Dates acted if not for whole
**year **
Name of person (or body) entitled
to appoint trustee (ifany)
Kathleen McCall Chairman
Richard Simpson Trustee
Joyce Wood Trustee

Names of the trustees for the charity, if any, (for example, any custodian trustees)

Name Dates acted if not for whole year

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Names and addresses of advisers (Optional information)
Type of adviser
Name
Address
Names and addresses of advisers (Optional information)
Type of adviser
Name
Address
Names and addresses of advisers (Optional information)
Type of adviser
Name
Address

Name of chief executive or names of senior staff members (Optional information)

Section B Structure, governance and management

Description of the charity’s trusts

Type of governing document

CIO Foundation Model

(eg. trust deed, constitution) CHARITABLE INCORPORATED ORGANISATION How the charity is constituted

Appointed by Existing Trustees Trustee selection methods

Additional governance issues (Optional information)

You may choose to include additional information, where relevant, about:

Invest in ME Research (IiMER) works to build relationships nationally and internationally with other organisations who promote similar aims.

The charity is a founding member and chair for sixteen years of the European ME Alliance, a collaboration of national patient organisations and charities across Europe.

The charity also has cultivated links to many organisations, researchers, clinicians and healthcare staff and initiated, and continues to support European groups of researchers, clinicians and young researchers who will work together.

Section C Objectives and activities

Summary of the objects of the charity set out in its governing document

To promote and protect the well-being of sufferers of ME. To advance the education of the public in relation to ME. To promote research into causes and treatment of ME.

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Summary of the main
activities undertaken for the
public benefit in relation to
these objects (include within
this section the statutory
declaration that trustees have
had regard to the guidance
issued by the Charity
Commission on public
benefit)
The main activities are–
Organisation of annual public International ME Conference weeks that
attract doctors, scientists, researchers, patients and carers from around
the world to collaborate and share knowledge about ME.
Organisation of international research colloquia to encourage new
collaborative and cooperative possibilities for research into ME.
Creation and development of network of young researchers for ME.
Foundation and support of a collaborative European ME Research Group
network for researchers to come together.
Foundation and support of a collaborative European ME Clinicians
Council network for European clinicians to come together to build
knowledge and expertise around ME.
Production of educational material (videos, booklets, journals and
guidelines) related to ME.
Finding, facilitating and funding of biomedical research into ME.
Continuing development of the Centre of Excellence for ME model that
the charity has proposed and championed since 2011.
Initiation of awareness and fund-raising activities regarding ME.
Maintenance of web sites for the charity, and European ME organisations
containing educational information regarding ME and our initiatives and
conferences
Creation and administering of webinars to enhance education of the
public and to disseminate information around Europe regarding ME.
Advocacy work to help patients in need. Participation in DHSC working
group to develop policies for ME.
Distribution of regular newsletters to patient groups, patients, healthcare
staff, media, politicians and general public regarding ME.
Board member of the European ME Alliance and participating in
European collaborative projects regarding awareness of ME.

Additional details of objectives and activities (Optional information)

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The trustees and volunteers perform all of the charity’s work for free.

The charity does not have any salaried staff.

The charity endeavours to provide services, products and information for free or as near to cost price as possible, to avoid ME patients having to bear additional burdens around costs.

You may choose to include further statements, where relevant, about:

The charity has a Biomedical Research Fund that allows grants for research projects to be made in an attempt to initiate more biomedical research into Myalgic Encephalomyelitis.

The charity has a peer review process for examining applications for grants.

The charity attempts to initiate more biomedical research into Myalgic Encephalomyelitis with an emphasis on international collaboration.

The charity has published our policy on grant making on our web site.

We are continuing to support our proposal to develop a UK/European Centre of Excellence for ME that will include examinations and research facility into ME and would perform biomedical research into the disease and allow proper examinations and diagnosis for ME patients.

We have initiated several major research studies for ME that take place at major UK institutes.

Section D Achievements and performance

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Section D Achievements and performance Invest in ME Research Summary of the main achievements of the charity Period: October 2024 - September 2025 during the year Invest in ME Research (IiMER) is a small charity with a clear strategy of research, education and advocacy, always aiming to look at the bigger picture and facilitate meaningful change through innovation, ideas and determination. The charity remains dedicated to improving the lives of people with myalgic encephalomyelitis (ME), as well as their families and carers. No salaries have ever been paid by IiMER; all work is performed by volunteers. There is no intention to employ a CEO or support staff. This ensures that the maximum possible funding is directed toward our essential aims: biomedical research into ME and events that facilitate education and collaboration. The scale of activity set out below was delivered entirely by volunteer effort. 1. Building the case for European Horizon funding — DISCOVER-ME The charity's most substantial undertaking of the year was the work behind what would become the DISCOVER-ME consortium application to the EU Horizon Europe programme. This was not a single event but a sustained campaign of coordination stretching across the year. IiMER took the lead in identifying and pulling together the European ME Research Group (EMERG) members needed to form a credible consortium, and arranged dedicated in-person meetings during ME Conference Week specifically to progress the proposal. Throughout the year the charity continued to campaign among EMERG members to build and sustain the commitment needed to keep a multi-country consortium of independent researchers aligned behind a single application. The charity also identified and recommended the specialist grant-writing consultancy engaged to prepare the submission, and funded the consultancy's fees itself. None of this work is visible in a funding outcome, since it precedes any decision, but without the consortiumbuilding, the sustained campaigning, and the sourcing and funding of professional application support, the application would not have been made at all. The application was submitted within this reporting period. 2. Research The charity has continued to promote the development of a Centre of Excellence for ME at the Norwich Research Park. In January 2025 the charity published an article, "A Decade Developing the CofEforME", marking ten years of this work and setting out the case for continued investment. The charity's fellowships at the Quadram Institute Bioscience continued throughout the year: the Ian Gibson Fellowship for ME, held by Dr Katharine Seton, and the LunaNova-funded fellowship, held by Dr Krishani Perera. Research emerging from this fellowship programme continued to be published and reported, including a paper from IiMERfunded research reported in February 2025. These fellowships represent a direct, ongoing return on the charity's decade of investment in building research capacity at Norwich. Rik Haagmans, one of the charity's funded PhD studentships at the

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Section D Achievements and performance

Quadram Institute, completed his doctoral research during this period. Building directly on this work, Rik and the Quadram Institute successfully applied to the Dutch ZonMW research agency, and he has since established an ongoing collaboration with the Dutch ME/CFS Cohort and Biobank (NMCB) programme, extending the charity's funded research into an active international partnership between Norwich and the Netherlands. 3. Education — ME Conference Week 2025 The charity organised and delivered ME Conference Week 2025 (April 2025) — the only international conference week of its kind dedicated to ME, spanning five days and comprising the Young EMERG Workshop, the 14th Biomedical Research into ME Colloquium (BRMEC14), and the 17th Invest in ME International Conference (IIMEC17).

BRMEC14 was the largest and most productive colloquium in the series to date. Presenters and programme were announced in February 2025, following the considerable, and far from trivial, work of identifying and securing researchers willing to present. The colloquium was awarded CPD accreditation in April 2025. IIMEC17: registration opened in February 2025, speakers were announced in May 2025 (again the product of sustained outreach to secure a credible international speaker programme), and the conference was awarded full CPD accreditation in May 2025. Recordings of the conference were produced and made freely available, with videos published in July 2025. This is a deliberate choice by the charity: making the full research programme available at no cost means patients, carers and others who cannot travel or afford registration are able to see the same research presentations as delegates, extending the conference's educational reach well beyond those in the room. Young EMERG Workshop: held in May 2025 as part of Conference Week, with reflections on the workshop published in September 2025. The charity also began organising and supporting a further Young EMERG workshop, held in Vienna, continuing its role in building a European network of early-career ME researchers beyond the UK conference itself. Summer bursaries for students were announced in February 2025, continuing the charity's support for early-career researchers. International ME Awareness Month/Day was marked in May 2025, and reflections on the conference week were published in June 2025. 4. Advocacy Following the conclusion of the DHSC Interim Delivery Plan Research Working Group in April 2024 (reported in last year's Trustees' Annual Report), the charity offered to host a meeting bringing together NIHR, MRC and researchers, to keep momentum behind a coordinated national research strategy for ME. No reply was received from MRC, and the charity has had no further involvement in this area since. No DHSC or

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Section D Achievements and performance

MRC-related activity therefore falls within the October 2024 to September 2025 reporting period.

5. Communications

The charity maintained its public communications throughout the year via its website, newsletters and social media, including establishing a presence on Bluesky (November 2024).

Conclusion

This report covers a single year in the life of a charity of volunteers with a clear strategy. In that year, without a single paid member of staff, volunteers coordinated a multi-country European research consortium and secured its Horizon Europe funding application; sustained two ongoing research fellowships at a UK institute, producing published science; saw one of its own funded PhD studentships completed, going on to establish a new international research collaboration with the Netherlands; identified, negotiated with and funded the specialist support needed to make a serious EU application possible; and planned, organised and delivered the only five-day international conference and colloquium week dedicated to ME anywhere in the world, complete with independent CPD accreditation. The resulting research was then recorded and released free of charge, so that patients and carers too unwell to travel, and researchers and clinicians without a conference budget, could see the same work as those in the auditorium.

This represents considerable voluntary effort, applied consistently to a clear strategy. That strategy is working. It happened because a small charity with wonderful supporters gave the organisational, diplomatic and administrative skill this cause demanded, year after year. The Trustees consider this an exceptional return, for patients and for research into ME, on a charity that carries no unnecessary overhead and is focused on results

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Section E Financial review

Brief statement of the charity’s policy on reserves

Our reserves are held to meet expected and unexpected bills and to cover running costs and printing/stationery costs. Our objective is to use as much of our resources for the facilitation and implementation of biomedical research into ME and to raise awareness of the disease.

Details of any funds materially in deficit

Further financial review details (Optional information)

The Trustees feel that it is important to try to make all of the educational material and information that we create or facilitate (whether by way of conferences, webinars or other educational material) accessible to patients and their families for free or as cheaply as possible, without compromising professionalism or standards. Many patients and carers are unable to work due to the effects of this devastating neurological disease and the lack of a proper research strategy to create treatments.

You may choose to include additional information, where relevant about:

The charity continues to feel that better education of healthcare staff via a strategy of biomedical research into ME is the key to improving conditions for people with ME and their families.

IiMER aims to provide all our work for free or at cost price. We are an independent charity whose focus is on better education, better awareness, and a strategy of high-quality biomedical research into myalgic encephalomyelitis.

We hope to continue to find, fund and facilitate research and provide a means to raise more awareness of this disease – ME – and so enable a rapid resolution to be created by provision of treatments and cures from high-quality science. This benefits not only people with ME, their carers and families, but also society in general.

The Trustees also note that administrative costs are kept to an absolute minimum. No salaries are paid, and all work is carried out by volunteers, ensuring donations are used efficiently to support research, education, and advocacy. The Trustees are mindful of the need to maintain sufficient reserves to meet ongoing research commitments and to provide stability for future projects. The charity remains independent and does not accept funding that would compromise its aims or values. All income is used to further the charity’s objectives and to benefit people with ME, their carers, and families.

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Section F Other optional information

Section G Declaration

The trustees declare that they have approved the trustees’ report above.

Signed on behalf of the charity’s trustees

Signature(s)
Full name(s)
Position (eg Secretary, Chair,
etc)
Date
Kathleen McCall Richard Simpson

Chair
Trustee
7thJuly 2026
6thJuly 2026
7thJuly 2026

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Charity Name No (if any)
INVEST in ME RESEARCH 1153730

Receipts and payments accounts

CC16a

For the period
from
Period start date
1-Oct-24
To Period end date
30-Sep-25

Section A Receipts and payments

Unrestricted Restricted Endowment Total funds Last year funds funds funds to the nearest £ to the nearest £ to the nearest £ to the nearest £ to the nearest £

A1 Receipts

A1 Receipts
General Donation,Legacies and Grants 95,935 - - 95,935 94,944
Conferences and meetings 23,546 - - 23,546 16,915
Brochure(CG & QQ & Journal etc) - - - - 67
Tax refund / Gift Aid 1,638 - - 1,638 1,019
- - - - -
- - - - -
- - - - -
- - - - -
Sub total(Gross income for AR) 121,119
- - 121,119 112,945
A2 Asset and investment sales,
(see table).
- - - -
- - - - -
Sub total - - - - -
**Total receipts ** 121,119 - - 121,119 112,945

A3 Payments

Meetings and conferences
Postage, Packaging, Stationery
Printing of Brochures, Books &
Guidelines
Governance, Web Services,
Advertising
97,805 - - 97,805 85,477
715 - - 715 777
474 - - 474 417
2,919 - - 2,919 3,940
Fundraising Products/Equipment 277 - - 277 216
Biomedical Research 149,353 - - 149,353 40,710
Bank Charges 346 - -
-
-
-
346 158
- - - -
- - - -
Sub total 251,889 - 251,889 131,695
A4 Asset and investment
purchases, (see table)
- - - -
- - - -
Sub total
- - - - -
**Total payments ** 251,889 - - 251,889 131,695
Net of receipts/(payments)
- 130,770 - - - 130,770 - 18,750
A5 Transfers between funds
- - - - -
A6 Cash funds last year end
419,377 - - 419,377 -
Cash funds this year end
288,607 - - 288,607 - 18,750

Section B Statement of assets and liabilities at the end of the period

Categories
B1 Cash funds
B2 Other monetary assets
B3 Investment assets
B4 Assets retained for the
charity’s own use
Details
Lloyds
Details
Details
Details
Total cash funds
(agree balances with receipts and payments
account(s))
to nearest £
288,607
-
-
288,607
OK
to nearest £
-
-
-
-
-
-
Unrestricted
funds
Unrestricted
funds
Fund to which
asset belongs
Fund to which
asset belongs
to nearest £
-
-
-
-
OK
to nearest £
-
-
-
-
-
-
Cost (optional)
-
-
-
-
-
Cost (optional)
-
-
-
-
-
-
-
-
-
Restricted
funds
Restricted
funds
to nearest £
Endowment
funds
-
-
-
-
OK
to nearest £
Endowment
funds
-
-
-
-
-
-
Current value
(optional)
-
-
-
-
-
Current value
(optional)
- -
- -
- -
- -
- -
- -
- -
- -
- -

B5 Liabilities

Signed by one or two trustees on behalf of all the trustees

Details Fund to which
liability relates
-
-
-
-
-
Amount due
(optional)
When due
(optional)
-
-
-
-
-
Signature
K.McCall
Richard
Print Name
Kathleen McCall
Richard Simpson
Date of
approval
Kathleen McCall 7/5/2026
Richard Simpson 7/5/2026

Independent examiner's report on the accounts

Section A Independent Examiner’s Report

Report to the trustees/ Charity Name INVEST in ME RESEARCH members of On accounts for the year 30th September 2025 Charity no 1153730 ended (if any) Set out on pages 1 and 2 (remember to include the page numbers of additional sheets)

I report in respect of my examination of the Trust’s accounts carried out under section 145 of the 2011 Act and in carrying out my examination, I have followed the applicable Directions given by the Charity Commission under section 145(5)(b) of the Act.

Independent examiner's statement

I have completed my examination. I confirm that no material matters have come to my attention (other than that disclosed below *) in connection with the examination which gives me cause to believe that in, any material respect:

I have no concerns and have come across no other matters in connection with the examination to which attention should be drawn in order to enable a proper understanding of the accounts to be reached.

Signed: Date: 11/07/2026 Name: PAUL BOOTH Relevant professional Recruitment Consultant qualification(s) or body (if any): Address: 30 Provene Gardens Waltham Chase SO32 2LE

1

October 2018

IER

Section B Disclosure

Only complete if the examiner needs to highlight matters of concern (see CC32, Independent examination of charity accounts: directions and guidance for examiners).

Give here brief details of any items that the examiner wishes to disclose .

2

October 2018

IER