25% ME Group at IACFSME Conference
25% ME Group at IACFSME Conference Advocacy worker, Helen Baxter attended the International Association for Chronic Fatigue Syndrome/Myalgic…
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Ensuring the Voice of the Very Severely Affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patient Is Heard in Research—A Research Model.
Abstract Most of the research about Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has focused on ambulant patients who are…
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The 25% ME Group’s Season’s greetings video
E D I T . The video has been viewed over 250 times in the last 24 hours!…
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An Introduction For Physicians and Patient* To Modern SPECT Technology
How to Understand Segami Brain SPECT on M.E. and toxic chemical injury patients. At the request of many…
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ME Awareness Day May 2020
WHAT IS ME AWARENESS DAY? May 12th is a well known date in the ME world as it…
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25 year anniversary of the 25% ME Group
This year marks the 25 year anniversary of the 25% ME Group, the only charity concerned specifically with…
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The impact of profound Multiple Chemical Sensitivity in Severe ME
A Painfully Nuanced Life: The impact of profound Multiple Chemical Sensitivity in Severe ME. (Published in the latest…
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New Guideline on ‘ME/CFS’ in Development
The National Institute for Health and Care Excellence – commonly abbreviated to ‘NICE’ – have recently begun the…
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25% ME Group Launches New Website
Sound the fanfares!! We are delighted to launch our new website, which is now live, and also to…
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Severe ME Awareness Day, 8th August 2014 – ME Cover up!
If you want to raise awareness of the cover up of our serious neurological disease, please share a…