British Medical Journal: How can I support my colleague returning to work with Long Covid?
“Remember that no two people with Long Covid will be […]
News
America: Post-Acute Infection Syndromes will be the Focus of New Center at Yale School of Medicine
The new centre will investigate Long Covid, ME/CFS, and post-treatment Lyme disease.
Advertising Standards: Chrysalis Effect cannot claim ME/CFS recovery!
Advertising Standards: Chrysalis Effect cannot claim ME/CFS recovery! Read More »
The ME Association had made a complaint to the Advertising
Research: Developing a Blood Cell-Based Diagnostic Test for ME/CFS Using Peripheral Blood Mononuclear Cells
The following research was funded by the ME Association Ramsay
Guardian: UK scientists find link between proteins related to blood clots and Long Covid
Guardian: UK scientists find link between proteins related to blood clots and Long Covid Read More »
ME Association Comment: “Interesting new research from the University of
TIME: Long COVID Recovery Remains Rare
TIME: Long COVID Recovery Remains Rare Read More »
Since August 2020, David Putrino, director of rehabilitation innovation at
Research: Potential abnormalities found in home-based testing of everyday activities in ME/CFS
The following research was funded by the ME Association Ramsay
Research: A protein that disrupts a cell’s energy structure may be a culprit in ME/CFS (& Long Covid)
Researchers have identified a protein that’s present at unusually high levels in
Severe ME Week 2023: A parent’s perspective
Severe ME Week 2023: A parent’s perspective Read More »
Given the vast numbers of patients throughout the U.K. with
Severe ME Week 2023: Katie’s thoughts on relative improvements
Severe ME Week 2023: Katie’s thoughts on relative improvements Read More »
Living this life and deteriorating is hard beyond belief to
Severe ME Week 2023: John’s Story
Severe ME Week 2023: John’s Story Read More »
Conditions on the ward, similar to the other wards he
Severe ME Week 2023: Leanne’s Story
Severe ME Week 2023: Leanne’s Story Read More »
But the hardest symptoms to explain to people are how
Severe ME Week 2023: Sylvia’s Story
Severe ME Week 2023: Sylvia’s Story Read More »
The brain fog overwhelms my ability to comprehend the multiple
Severe ME Week 2023: Poems
Severe ME Week 2023: Poems Read More »
Poems – (3 of 4 website blogs) I will wait
Severe ME Week 2023: Katie’s Story
Severe ME Week 2023: Katie’s Story Read More »
It’s heart-breaking when the people we trust don’t trust us,
Severe ME Week 2023: Mike’s Story
Severe ME Week 2023: Mike’s Story Read More »
I have had severe M.E. for 26 years. I fluctuate
Department of Health Publish Interim ME/CFS Delivery Plan for Public Consultation
Department of Health Publish Interim ME/CFS Delivery Plan for Public Consultation Read More »
“This interim plan sets out the current problems to be
Severe ME Week 2023: Carla’s Story
Severe ME Week 2023: Carla’s Story Read More »
Last year, my whole life is shattered as I developed