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 […]
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 Read More »
Karen Buckley challenged herself to climb the Yorkshire Three Peaks
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 Read More »
Pretending everything is Normal It took seven months for John
Fiona Lowenstein writes in the Guardian of her experience of resting
Situations Vacant: We want a Welfare Benefits Adviser to join our team Read More »
The ME Association is a national charity that supports, informs, campaigns, and
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 Read More »
Are you a carer? I am. I am not a
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 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 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 Read More »
A major project is looking for your input. They want
Win this beautiful quilt stitched by people from the M.E.
The Real M.E. Campaign! Read More »
The Real M.E Campaign – Please send your photo and
The new NICE Clinical Guideline for ME/CFS will be published on 18
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
Nature Article: The four most urgent questions about long COVID Read More »
Scientists are starting to get insights into the lingering disorder
Research: Medical School Education on Myalgic Encephalomyelitis by Dr Nina Muirhead Read More »
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a complex multi-system disease with a significant impact on the quality of life of patients and their families, yet the majority of ME/CFS patients go unrecognised or undiagnosed.
Orthodoxy on trial: the pathogenesis of a diagnosis Read More »
David J Black looks at the shameful treatment of ME/CFS