Manx Radio supported the campaign for a local ME/CFS service with this easy-to-listen-to podcast.
Manx Radio turn up the volume for a specialist ME/CFS service on the Island Read More »
Manx Radio supported the campaign for a local ME/CFS service with this easy-to-listen-to podcast.
We challenge some appalling psychobabble that appeared in an article in The Observer (Guardian.com) in an otherwise fairly good piece about ME/CFS.
We demand changes to ‘Observer’ article Read More »
We challenge some appalling psychobabble that appeared in an article in The Observer (Guardian.com) in an otherwise fairly good piece about ME/CFS.
This is the final day of our Christmas Appeal, The matched funds have been used up. But donations to our Medical Education Campaign are still welcome.
The Big Give Christmas Challenge! Read More »
This is the final day of our Christmas Appeal, The matched funds have been used up. But donations to our Medical Education Campaign are still welcome.
Please make the MEA’s day! Buy these cards or a painting for Christmas.
Cards and paintings – please push the boat out a bit for the ME Association Read More »
Please make the MEA’s day! Buy these cards or a painting for Christmas.
In the news herself! Our magazine columnist Ev Francis writes for the Daily Telegraph and is filmed for a short BBC documentary.
Evan gets noticed by the media Read More »
In the news herself! Our magazine columnist Ev Francis writes for the Daily Telegraph and is filmed for a short BBC documentary.
There has been good news in recent days about potential vaccines for Covid-19 that could see an end to restrictions for people in the UK by Easter 2021…
Covid-19 Vaccine Developments & ME/CFS Read More »
There has been good news in recent days about potential vaccines for Covid-19 that could see an end to restrictions for people in the UK by Easter 2021…
This is a film for all seasons about pacing and activity management in people with ME – and in a certain type of Long Covid.
A new video on pacing and activity management – at such a critical time for us all Read More »
This is a film for all seasons about pacing and activity management in people with ME – and in a certain type of Long Covid.
This week 6 new studies about ME/CFS and Fibromyalgia were published including a small study from Canada that made the news…
The ME Association ME/CFS Research Round-up Read More »
This week 6 new studies about ME/CFS and Fibromyalgia were published including a small study from Canada that made the news…
ME Essential Magazine and the Christmas Supplement will be sent out to ME Association members this week. We hope there is something for everyone!
ME Essential Magazine & the Christmas Supplement will be with Members very soon! Read More »
ME Essential Magazine and the Christmas Supplement will be sent out to ME Association members this week. We hope there is something for everyone!
We hear from someone with severe ME who describes what Post-Exertional Malaise feels like and the measures that can help when in this situation…
ME and Post-Exertional Malaise: “It is much more than fatigue and stiffness…” Read More »
We hear from someone with severe ME who describes what Post-Exertional Malaise feels like and the measures that can help when in this situation…
We have updated the range of free leaflets about Covid-19/ME/CFS and the current restrictions and include a new leaflet aimed at Students…
ME Association Covid-19 & ME/CFS Free Range of Leaflets Read More »
We have updated the range of free leaflets about Covid-19/ME/CFS and the current restrictions and include a new leaflet aimed at Students…
In the first week of December, any donation to the Big Give Appeal will be doubled! Help us to change the medical mindset within the NHS…
Get Ready for The Big Give Christmas Appeal! It’s Only 2 Weeks Away… Read More »
In the first week of December, any donation to the Big Give Appeal will be doubled! Help us to change the medical mindset within the NHS…
Emma Roberts has a son, George, who has M.E. She has created special Christmas card designs to help raise money for the ME Association.
From the West Country – A generous Christmas offer to help the ME Association Read More »
Emma Roberts has a son, George, who has M.E. She has created special Christmas card designs to help raise money for the ME Association.
Eight new studies have been published and we highlight several of them including one about epigenetics and ME/CFS,
The ME Association ME/CFS Research Round-up Read More »
Eight new studies have been published and we highlight several of them including one about epigenetics and ME/CFS,
The ME Association is recruiting for a new Webmaster – someone who can look after the website and website shop and grow its online presence…
Situations Vacant: We want a Webmaster to join the ME Association team! Read More »
The ME Association is recruiting for a new Webmaster – someone who can look after the website and website shop and grow its online presence…
Graded exercise therapy should no longer be offered for the treatment of ME/CFS, says NICE in its draft clinical guidelines.
Graded exercise therapy should no longer be offered for the treatment of ME/CFS, says NICE in its draft clinical guidelines.
The NICE stakeholder consultation process begins today. You can take part and help produce the new clinical guideline on ME/CFS…
What do you think about the new NICE Clinical Guideline on ME/CFS? Read More »
The NICE stakeholder consultation process begins today. You can take part and help produce the new clinical guideline on ME/CFS…
The new NICE guideline has removed graded exercise as a recommended management option…
NICE Press Statement & Media Coverage of New Clinical Guideline on ME/CFS Read More »
The new NICE guideline has removed graded exercise as a recommended management option…
We report on 5 new research studies and highlight the discovery of bioenergetic defects in the skeletal muscle of people with ME/CFS.
The ME Association ME/CFS Research Round-up Read More »
We report on 5 new research studies and highlight the discovery of bioenergetic defects in the skeletal muscle of people with ME/CFS.
We seek a specialist to manage the charity’s growing social media. It is a full-time position that enables you to work from home…
We seek a specialist to manage the charity’s growing social media. It is a full-time position that enables you to work from home…
