The ME Association ME/CFS Research Round-up
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…
Mobility
Severe ME: Why is improvement subject to such harsh judgement and not celebrated?
Severe ME: Why is improvement subject to such harsh judgement and not celebrated? Read More »
“Having M.E. robs us of just about everything, but not the ability to be supportive or kind. We are a community, and it should be us against the world not us against each other.”
ME Awareness: The Lost Years by Wendy Coxhill | 11 May 2020
ME Awareness: The Lost Years by Wendy Coxhill | 11 May 2020 Read More »
“The first big challenge was when I became wheelchair-bound 3 years ago. The next loss was when I could no longer read or watch a film.”
Relationship between physiotherapists and people with M.E. is poor but there is potential to improve | 22 August 2019
Physios 4 ME report on the results from the MEA website survey that took place in July.
Very Severe ME: It’s Time for Something New! By Greg Crowhurst | 16 August 2019
Very Severe ME: It’s Time for Something New! By Greg Crowhurst | 16 August 2019 Read More »
I have cared day and night for my wife who has lain in unspeakable torment, torture and agony, for twenty-six years.