I am always pleased to hear from visitors therefore please do not hesitate to contact me at the address above or using this e-mail form. I usually check my mailbox daily although this is health and time dependant. Alternatively, you can talk to me on Skype by clicking the Chat button on the bottom right of your screen. M.E. Support is not a charity and it does not have a postal address or telephone number.
Do you need help and advice or would you like to contribute to the site? Are you an organisation with a upcoming event or would you like to exchange links? I also welcome your comments and suggestions regarding any aspect of M.E. Support. The information you provide will be entirely confidential and treated with the strictest confidence.
M.E. Support does not offer membership, however, you might like to subscribe to the Newsletter or join the Facebook Page. Please read the M.E. Organisations page if you are looking for local support or an 'M.E. friendly' medical practitioner. Lastly, please refer to M.E. Awareness for shopping facilities and free promotional material.
M.E. My Story is a personal account of life with this
debilitating neurological disease.
This revealing article was published in 2001 and recently updated.
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5 Feb 2014
Tymes Trust News
4 Feb 2014
M.E. Criteria & clinical guidelines
1 Feb 2014
Videos from the Institute of Medicine
31 Jan 2014
Does CFS Need A New Name?
28 Jan 2014
DePaul CFS Grant
28 Jan 2014
How "CFS" Obscures A Serious Illnes
25 Jan 2014
25 Jan 2014
Win £20 of products!
How to Help
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