British Medical Journal: Working together to find the cause & effective treatments for ME/CFS by Dr Charles Shepherd
As a charity that funds biomedical research into myalgic encephalomyelitis/chronic […]
Research Summary – Passive transfer of fibromyalgia symptoms from patients to mice – July 2021
A recent publication by Goebel et al. with research carried
Scientists raise hopes of blood test for long Covid
Scientists raise hopes of blood test for long Covid Read More »
Extracts of an article in The Medical Device Network. Long
Announcing the Launch of Doctors with M.E.
Announcing the Launch of Doctors with M.E. Read More »
Mission and Values To improve patient outcomes worldwide by empowering
Announcing The Howes Goudsmit Prize for Severe ME Research
Announcing The Howes Goudsmit Prize for Severe ME Research Read More »
The ME Association is pleased to announce the establishment of
But you did it before… Explaining M.E. by Mahli Quinn
But you did it before… Explaining M.E. by Mahli Quinn Read More »
Members of the ME Association will already have seen Mahli
Open Letters to Healthcare Professionals from people with ME/CFS – Part 10: Teri
Open Letters to Healthcare Professionals from people with ME/CFS – Part 10: Teri Read More »
Seeing what’s happened with Long Covid has been awful. It is also frustrating watching the scientific effort now to find a cure when M.E. has been ignored for so long…
BMJ Rapid Response Re: ME/CFS and Long Covid: Moving beyond the controversy – by Dr Charles Shepherd
An article by Melanie Newman was published in the British
The Telegraph: Everything we know about long Covid
The Telegraph: Everything we know about long Covid Read More »
A new study reveals that a third of Covid sufferers
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 due to be published on
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
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.
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