My Severe ME by Alison Love
It all started for me in 1992, when I was […]
My Severe ME by Alison Love Read More »
It all started for me in 1992, when I was
It all started for me in 1992, when I was […]
My Severe ME by Alison Love Read More »
It all started for me in 1992, when I was
The album is out on Saturday, but the single is out now! Help Kara raise funds for the Post-Mortem Tissue Bank to advance vital research into M.E.
Music industry backs Kara Jane’s bid for MEA charity album chart success Read More »
The album is out on Saturday, but the single is out now! Help Kara raise funds for the Post-Mortem Tissue Bank to advance vital research into M.E.
We asked those who suffer with Severe M.E if they would like to submit their stories to be published on the ME Association website blog.
The Untold Stories: Severe ME Week 2020 Read More »
We asked those who suffer with Severe M.E if they would like to submit their stories to be published on the ME Association website blog.
“It is incessant, inescapable torture. You are trapped. Completely powerless. You’re in agony with countless unbearable symptoms…”
How it feels to have Very Severe M.E. by Ruth Braham Read More »
“It is incessant, inescapable torture. You are trapped. Completely powerless. You’re in agony with countless unbearable symptoms…”
In this introduction you will find a discussion about the need for suitable healthcare. Also background about severe and very severe M.E. and the support that is available.
Severe ME Week: How might healthcare be improved? Read More »
In this introduction you will find a discussion about the need for suitable healthcare. Also background about severe and very severe M.E. and the support that is available.
We have updated the central index of ME/CFS published research for July, and include 4 new studies published this week.
The ME Association End of Week Research Round-up and Index Update Read More »
We have updated the central index of ME/CFS published research for July, and include 4 new studies published this week.
Holly aged 9, has written about her mum, Chantalle, and explains what life is like being the daughter of a parent with M.E.
My Mummy and M.E. by Holly Peretti Read More »
Holly aged 9, has written about her mum, Chantalle, and explains what life is like being the daughter of a parent with M.E.
The IACFS/ME Virtual Conference is open to all and will be held on Friday 21 August from 3.00PM – 8.30PM UK time.
Register Now! The International Association CFS/ME Virtual Conference Read More »
The IACFS/ME Virtual Conference is open to all and will be held on Friday 21 August from 3.00PM – 8.30PM UK time.
Chris Ponting talks about the DecodeME study that seeks to understand the causes of M.E. and could help advance the discovery of effective treatments.
Meet The Scientist: Professor Chris Ponting – DecodeME Read More »
Chris Ponting talks about the DecodeME study that seeks to understand the causes of M.E. and could help advance the discovery of effective treatments.
Dr Charles Shepherd explains why we have been devoting so much time and effort to covering issues relating to Post-COVID Syndromes.
Update: Post-Covid Fatigue, Post/Long-Covid Syndromes, and ME/CFS Read More »
Dr Charles Shepherd explains why we have been devoting so much time and effort to covering issues relating to Post-COVID Syndromes.