SKY News: ‘How long COVID ruined my life, from crushing fatigue to brain fog,’ with Dr Charles Shepherd
Sky’s technology correspondent Rowland Manthorpe has suffered with long COVID […]
Press Release: The ME Association is NOT asking for money this Christmas!
Press Release: The ME Association is NOT asking for money this Christmas! Read More »
This Christmas national charity the ME Association will be bucking
Research: Melatonin as Possible Treatment for Long Covid and ME/CFS Symptoms
Research: Melatonin as Possible Treatment for Long Covid and ME/CFS Symptoms Read More »
ME Association Comment This is a useful and interesting review
Cost of Living Crisis: Leading Neurological Charities Write to Chancellor ahead of Autumn Budget
Leading neurological charities including The ME Association have come together
The Irish Times: ‘I spend 20 hours a day lying down. I have 4 upright hours in the day’
The Irish Times: ‘I spend 20 hours a day lying down. I have 4 upright hours in the day’ Read More »
The Irish Times provides a comprehensive report on Myalgic Encephalomyelitis/Chronic
Research priorities for ME/CFS: the results of a James Lind alliance priority setting exercise
Members of the James Lind Alliance Priority Setting Partnership for
The Lightning Process should not be used by GPs to treat ME/CFS
The Lightning Process should not be used by GPs to treat ME/CFS Read More »
In England, the National Institute for Health and Care Excellence
Severe ME Week: “ME has turned my life upside down. But I hope I can recover to some extent and do the things I enjoyed once more…”
People who are severely or very severely affected by ME/CFS
Severe ME Week: “I was locked inside a shell that was too weak to protect me but too strong to escape…”
People who are severely or very severely affected by ME/CFS
Severe ME Week: “I had carers years ago from an agency, but it was difficult as they couldn’t understand my needs…”
People who are severely or very severely affected by ME/CFS
Severe ME Week: “I’m lonely, miserable, bored, constantly exhausted, and always in pain. And my brain no longer functions the way it used to…”
People who are severely or very severely affected by ME/CFS
Severe ME Week: “My 74-year-old mum does most things for me…”
Severe ME Week: “My 74-year-old mum does most things for me…” Read More »
People who are severely or very severely affected by ME/CFS
IACFS/ME Conference (4): Clinicians Can Help People With Severe ME/CFS, Even Unseen
IACFS/ME Conference (4): Clinicians Can Help People With Severe ME/CFS, Even Unseen Read More »
By Miriam E. Tucker, Medscape News, 05 August 2022 People
Severe ME Week: “I often need assistance to even make it to the bathroom…”
Severe ME Week: “I often need assistance to even make it to the bathroom…” Read More »
People who are severely or very severely affected by ME/CFS
IACFS/ME Conference (3): ME/CFS and Long COVID “Frighteningly Similar, if Not Identical”
IACFS/ME Conference (3): ME/CFS and Long COVID “Frighteningly Similar, if Not Identical” Read More »
By Miriam E. Tucker, Medscape News, 05 August 2022 Data
Severe ME Week: The inability to initiate let alone complete normal everyday activities…
Severe ME Week: The inability to initiate let alone complete normal everyday activities… Read More »
People who are severely or very severely affected by ME/CFS
Severe ME Week: Howes Goudsmit Prize Awarded to Producers of ‘Dialogues of a Neglected Illness’!
The ME Association is pleased to announce the 2022 Howes
IACFS/ME Conference (2): Increasing Data Link ME/CFS, Long COVID, and Dysautonomia
IACFS/ME Conference (2): Increasing Data Link ME/CFS, Long COVID, and Dysautonomia Read More »
By Miriam E. Tucker, Medscape News, 05 August 2022 Emerging
Severe ME Week: “The invisible me that nobody sees…” a Poem by Rachel Beadle
Severe ME Week: “The invisible me that nobody sees…” a Poem by Rachel Beadle Read More »
“The invisible me that nobody sees,because it’s uncomfortable to acknowledge,the