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Join our community:
Together we can make the UK a better place for people with ME/CFS

From just £2.00 a month you can help support others affected by M.E. and will receive the excellent and exclusive ME Essential magazine delivered straight to your door.

We recognise that your personal endorsement of our cause is important and we will do all that we can to support the needs of our members.

“The ME Association has been there since I first became ill and given support when all else has failed. Its continuing presence is very important to me.”

Member comment.

We support, inform, advocate and invest in biomedical research…

Real People. Real Disease. Real M.E.

Subscriptions are a vital part of our charity income and – together with donations – they allow us to help make the UK a better place for people with M.E.

Moreover, the more members we have, the more representative we can be – which is especially useful when we take part in debates, we decide to launch a specific campaign or seek to raise awareness in Government or with medical authorities.

You don’t have to be personally affected by M.E. to join the ME Association. Membership is available to carers, family-members, and anyone with a professional interest in the condition.

“If it wasn’t for the ME Association I don’t think I would have been able to move from being very severely ill to where I am today.”

“Members of the charity have been very quick to help me with problems and especially Dr Shepherd, as he is so busy and trying to do so much despite his own poor health. I’m very grateful to all the team.”

“I like and trust that many people working for the ME Association have first-hand knowledge and experience of M.E.”

“I like that it has regular medical input from Dr Shepherd, who seems like a reliable doctor with a thorough knowledge of ME and ongoing interest in current research.”

“The ME Association makes me feel less isolated. I believe that ME is real and physical, and I like that the ME Association is wholeheartedly behind research to prove this.”

Members comments.

Membership Subscriptions

Full Membership is available to all adults with ME/CFS, carers and anyone with an interest in the disease.

  • £18.00 (UK residents and BFPO)
  • £24.00 (Mainland Europe including Republic of Ireland)
  • £30.00 (Rest of the World)

Each full member is entitled to vote at our Annual and Extraordinary General Meetings.


Real People. Real Disease. Real M.E.

Special Offer

If you join by annual standing order, you can select £10 worth of leaflets from the largest stock of literature held by any M.E. charity in the UK.

In order to take advantage of this offer you will also need to download, complete, and return the Membership Application Form, together with the form indicating your chosen selection of free leaflets.

How to Join

You can join the ME Association and pay your annual subscription in several ways:

  • Debit or credit card via our website shop,
  • Debit or credit card by phone to head office (01280 818964 between 9.30am and 3.00pm, Monday-Friday),
  • Download and complete the Membership Application Form, and pay by debit or credit card, cheque or postal order,
  • Download and complete the Membership Application Form, and pay by annual standing order (and qualify for £10 worth of free leaflets).

Membership Pack

When we have received your subscription, we will send you:

  • A copy of the latest issue of our magazine, ME Essential,
  • An information sheet: ‘Where to find benefits’,
  • An information sheet listing a number of books which you may find helpful, and,
  • If you have paid by annual standing order, your selection of £10 worth of free leaflets.

Why You Should Join

We are championed by the UK’s best-known M.E. expert and campaigner – Dr Charles Shepherd – our honorary medical adviser and a trustee of the ME Association.

Dr Charles Shepherd, Hon. Medical Adviser, ME Association.

Dr Shepherd not only has personal experience of the disease, but also manages to:

  • regularly provide updated medical information – that we publish as leaflets available in the website shop or as articles in our members magazine, or on our website and social media,write and update our authoritative clinical and research guide, now in it’s 10th edition,
  • represent the ME Association, e.g. as chair of the steering group for the UK ME/CFS Biobank, as an executive member of the CFS/ME Research Collaborative, and, as a member of Forward ME, which is chaired by the Countess of Mar,
  • provide key contributions to major publications, e.g. the NICE ME/CFS clinical guideline and review process, and other ME Association reports such as the widely cited publications relating to illness management,
  • 2017 Parliamentary presentation of the ‘Unrest’ documentary.

    attend key research and medical conferences, often presenting (e.g. at the 2018 RCGP conference), and always publishing reports for members and the wider patient community to read,

  • edit our very popular research reviews, that help lay audiences to better understand the research that is taking place into their illness,
  • be heavily involved in the UK promotion (pictured in Parliament) of the award-winning documentary ‘Unrest’ from Jennifer Brea and other advocacy efforts.

We are regarded as the UK’s premiere M.E. charity and actively campaign for greater recognition and understanding of the disease:

  • Real People. Real Disease. Real M.E.

    We recognise that M.E. is a physical disease,

  • Many of our trustees and staff are affected by M.E. or are primary carers for family members who have the disease, and this personal experience is reflected in everything we try to achieve,
  • We understand the nature of M.E. and how hard it is to live with the condition,
  • Our combined experience of M.E. and of the inequalities faced by this community, provide the main motivation for us to help others.

We fund biomedical research into M.E. and aim to discover effective treatments and a cure:

We work to secure improved health services that recognise the reality of M.E. and for better welfare support that is easier to obtain by those too ill to work or care for themselves.

We provide ME Connect, our flagship telephone and email service, which offers support and information to anyone affected by M.E:
  • ME Connect is available every day of the year – even on bank holidays – and has managed more than 35,000 calls since its inception in 2003.

We produce the best member’s magazine in the UK today:

  • ME Essential is delivered straight to your door and features exclusive interviews, medical and scientific updates and includes stories about how people cope with M.E. as well as member’s own stories and fundraising adventures.

Real People. Real Disease. Real M.E.

We listen to what our members – and those in the wider M.E. community – tell us about their experiences of this illness and the difficulties faced by a life with M.E.:

  • We feature a monthly survey on our website homepage that seeks feedback from people with M.E. about their lived experience,
  • We host very popular and open debates on our Facebook and Twitter pages,
  • We invite questions via Facebook, ME Connect, ME Essential, and head office,
  • We also formally canvass members and non-members about their feelings towards the ME Association and try to ensure we are meeting their needs.

“I found the information leaflets were excellent on dealing with work and benefit issues.”

“I was desperate for information that would give me good advice to help in any recovery I might make and found the magazine offered the best hope.”

“It stops me from feeling so alone. It is a very strong advocate for patients.”

“I really appreciate the extraordinary amount of work and effort that each of you dedicates to supporting our community.”

“I like most of all that you are consistent in your beliefs about this illness and vigilant on our behalf about negative media coverage…”

“It sticks to its guns about ME being a physical illness, not psychological, and continually fights against the prevailing NICE guideline re: CBT and GET.”

Members comments.

More reasons to join the ME Association

Real People. Real Disease. Real M.E.

We asked members why they joined the ME Association, and the top 5 reasons were:

  • I wanted a continuing source of reliable support and information
  • I agreed with what I felt was the ME Association ethos i.e. that M.E. is a real and physical disease
  • I wanted to belong to a charity that provided support, lobbying and biomedical research
  • I wanted to be part of a community which ensured I no longer felt isolated and alone
  • I wanted to contribute financially to the work of the ME Association

Note: The top 5 reasons for joining, and all the quotes shown on this page, were freely given as a result of a comprehensive stakeholder survey, that obtained views from members and non-members of the ME Association.


The ME Association

Please support our vital work

We are a national charity working hard to make the UK a better place for people whose lives have been devastated by an often-misunderstood neurological disease.

If you would like to support our efforts – particularly during ME Awareness Week – and help ensure we can continue to inform, support, advocate and invest in biomedical research, then please donate today.

Just click the image opposite and visit our JustGiving page for one-off donations, to establish a regular payment or to create your own fundraising event.

Or why not join the ME Association as a member and be part of our growing community? For a monthly (or annual) subscription you will also receive our exclusive ME Essential magazine.

Other pages in this section:


ME Association Registered Charity Number 801279


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