Open Letters to Healthcare Professionals from people with ME/CFS – Part 9 Gaynor
Open Letters to Healthcare Professionals from people with ME/CFS – Part 9 Gaynor Read More »
The new NICE Clinical Guideline for ME/CFS will be published on 18 […]
2021
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
The weekly research round-up now includes recent publications about ME/CFS
‘Medieval’ M.E. care on Isle of Man, says sufferer
‘Medieval’ M.E. care on Isle of Man, says sufferer Read More »
Article from Isle of Man Today published 28 May 2021
Emotions of carers who care for people with ME/CFS
Emotions of carers who care for people with ME/CFS Read More »
Knowing how to care I wish I knew how to
Karen smashed the Yorkshire Three Peaks
Karen smashed the Yorkshire Three Peaks Read More »
Karen Buckley challenged herself to climb the Yorkshire Three Peaks
Proud finale for the lady who had beetled back home to Bolton!
Proud finale for the lady who had beetled back home to Bolton! Read More »
Sarah Elsby is back in the fundraising frame – over a
The challenges carers face when caring for people with ME/CFS
The challenges carers face when caring for people with ME/CFS Read More »
Pretending everything is Normal It took seven months for John
Guardian Article: I rested my way to recovery from long Covid. I urge others to do the same
Fiona Lowenstein writes in the Guardian of her experience of resting
Open Letters to Healthcare Professionals from people with ME/CFS – Part 8 Andrew
Open Letters to Healthcare Professionals from people with ME/CFS – Part 8 Andrew Read More »
I’m Andrew and have had ME/CFS for over 20 years. It’s been a difficult road, but you have seen me over that time to try to help. Some of you have been helpful and some have been understanding, and I thank you for that.
Being a carer for someone with ME/CFS
Being a carer for someone with ME/CFS Read More »
Are you a carer? I am. I am not a
Long Covid and ME/CFS: Autoantibodies, neurotransmitters and autonomic nervous system dysfunction
The new paper in Nature looks at the possible role of two specific neurotransmitter receptor autoantibodies in Long COVID and ME/CFS
Guest Blog: The Shame
Guest Blog: The Shame Read More »
I’m ashamed to say I have M.E. I’ve collapsed in
Open Letters to Healthcare Professionals from people with ME/CFS – Part 7 Nancy
Open Letters to Healthcare Professionals from people with ME/CFS – Part 7 Nancy Read More »
Please be aware of the effects of going through the peri-menopause, and then the menopause, for women with ME.
ME/CFS Priority Setting Partnership: 2 weeks to send research ideas
ME/CFS Priority Setting Partnership: 2 weeks to send research ideas Read More »
A major project is looking for your input. They want
The Real M.E. Campaign!
The Real M.E. Campaign! Read More »
The Real M.E Campaign – Please send your photo and
MEA Research Review: Altered Endothelial Function in ME/CFS Blood Plasma
MEA Research Review: Altered Endothelial Function in ME/CFS Blood Plasma Read More »
A recent publication by Blauensteiner et al. based in Austria
Open Letters to Healthcare Professionals from people with ME/CFS – Part 6 Angela & Stuart
The new NICE Clinical Guideline for ME/CFS will be published on 18
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up
The ME Association ME/CFS (& Long Covid) Weekly Research Round-up Read More »
The weekly research round-up now includes recent publications about ME/CFS
Open Letters to Healthcare Professionals from people with ME/CFS – Part 5 Maryjane
Open Letters to Healthcare Professionals from people with ME/CFS – Part 5 Maryjane Read More »
The new NICE Clinical Guideline for ME/CFS will be published on 18
MEA Letter Published by The Times re: Why is Britain the Long Covid capital of the world?
Following a disappointing article from Josh Glancy that appeared in