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Want to learn more about this often-misunderstood neurological disease?

We have the following free leaflets available that we hope you will find useful:

If you have a query about symptoms, diagnosis, management etc. then please review the detailed website section: What is ME?

You will also find links to the medical leaflets we have available that are written by Dr Charles Shepherd and our other expert advisers.

ME Connect – Telephone and Email Helpline

“Most of our calls are from people who have ME, but we’re also here to help family or carers.”

The ME Association telephone helpline service is open every day of the year.

ME Connect is available from 10.00am – 12.00pm, 2.00pm – 4.00pm, 7.00pm – 9.00pm. 

Telephone 0844 576 5326 to speak to one of our fully-trained volunteers. 

You can also email with any queries you might have and we will reply as soon as we possibly can.

Please note:

  • We are a small medical charity and we do not have the capacity to answer long or complex questions relating to medical management, DWP benefit disputes and legal problems.
  • The ME Connect email service provides information and support and, where appropriate, signposting to further sources of help or information. Please try to limit your question to no more than 250 words.
  • We regret that Dr Shepherd cannot enter into personal correspondence on medical queries.
  • All communications are treated in the strictest of confidence.
  • Phone charges to 0844 numbers are determined by your telephone provider. Please check your contract for charging details.
  • The service charge is 7p a minute – from which the ME Association receives 3p – plus your provider’s access charge.
  • Calls from mobiles and other devices can be considerably more expensive than from a landline.

The Real M.E. photo campaign.

Administration

Our head office is managed by Gill Briody and her team and you can contact them by post, telephone or email and they will get back to you as soon as they can.

Address: The ME Association, 7 Apollo Office Court, Radclive Road, Gawcott, Bucks, MK18 4DF

Telephone: 01280 818964 weekdays, between 9.30am and 3.00pm. Email: Head Office.

Fundraising

Fundraising not only raises money for the ME Association. It is also a great opportunity to raise awareness of the disease beyond the M.E. community.

ME Awareness Week – 6-12th May 2019!

Let us know if you have an idea of what you want to do – or even if you don’t and need some help coming up with something. We can not only help you set things up, we can also help promote your event on our website and across social media.

Please review the information we have provided in the Get Involved section of the website.

Our fundraising manager, Helen Hyland, is available if you want to discuss any fundraising ideas or require support for your fundraising event. You can reach Helen by telephone (01280 838964), or by email.


The ME Association

Please help us to continue with 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 and ensure we are able to inform, support, advocate and invest in biomedical research, then please donate today.

Just click the image opposite to visit our JustGiving page for one-off donations or to establish a regular payment.

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.


ME Association Registered Charity Number 801279


New edition also available on Kindle!

Leaflets, books and other merchandise

Purchases can be made from our website shop, or by completing the 8-page Order Form and returning it to our head office.

Once you have paid for a leaflet online, you will be sent an email that is your receipt/invoice and also contains a link and password. This returns you to our website and allows you to download your leaflet.

If you think you haven’t received this email, it is worth checking your spam/junk folder to be sure, before contacting head office (see above for details).

More information about ordering our material can be found on the various pages in the website shop and on the order form.

Includes ‘Ask the doctor’ feature!

ME Essential

Members of the ME Association receive a quarterly magazine – ME Essential – delivered straight to their door.

This is a 50-page exclusive, featuring interviews, up-to-date medical and scientific research information and stories about how people cope with the disease.

If you have any queries or ideas for articles for ME Essential, or would like to advertise in the magazine or on this website, then please contact the editor by email.

Media Enquiries

For press enquiries, please contact our PR manager, John Siddle, by email or by phone (07598 032 845).

You might also like to read and download our Factsheet which provides important information about M.E. that can be useful background.

Membership

Dr Charles Shepherd, Trustee and Hon. Medical Adviser to the ME Association.

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.

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

If you are interested in joining the ME Association, you might want to first read the membership section of our website.

Note to existing members:
Please quote your membership number when making your enquiry (this will be on your letter confirming membership and also appears on the address label of your copy of ME Essential).

Ramsay Research Fund

Dr Melvin Ramsay, M.E. pioneer who also worked to establish the ME Association.

The ME Association has always regarded the promotion and funding of medical research to be a key priority, and we do this through The Ramsay Research Fund.

The fund was named after Dr Melvin Ramsay who brought this disease to the attention of the medical profession following an outbreak of M.E. at London’s Royal Free Hospital in 1955.

Dr Ramsay also helped establish the ME Association which was founded in 1978 and he remained closely involved with the charity until his death in 1990.

If you are a researcher interested in approaching us for a grant, or someone wanting to learn more about our approach to research, you might like to first read the research section of the website.

Any grant enquiries should first be directed to Dr Charles Shepherd, Hon. Medical Adviser, via the head office of the ME Association.

Website and social media

If you have any queries, or ideas to improve or update the information on our website or our Facebook and Twitter and Instagram pages, then please send an email to our content manager.


The ME Association

Please help us to continue with 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 and ensure we are able to inform, support, advocate and invest in biomedical research, then please donate today.

Just click the image opposite to visit our JustGiving page for one-off donations or to establish a regular payment.

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.


ME Association Registered Charity Number 801279


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