The Care Act and M.E. – Positive Decision by the Ombudsman and Case Study| 06 August 2019
This ombudsman decision shines a light on the difficulty that some people with M.E. face in obtaining social care.
This ombudsman decision shines a light on the difficulty that some people with M.E. face in obtaining social care.
Zoe was put under surveillance – monitors, lights on constantly, nurses watching her eat and humiliatingly insisting on escorting her to the loo…
ME Association July Summary of ME/CFS Published Research | 05 August 2019 Read More »
We’ve updated the central Research Index and feature 13 ME/CFS research studies from July 2019.
The Guardian: ME and the perils of internet activism | 29 July 2019 Read More »
This latest article continues to shine an uncritical spotlight on an issue that we really don’t think stands up to scrutiny…
MEA Summary Review: The Role of Mitochondria in ME/CFS | 13 July 2019 Read More »
This latest review looks at energy production, and the ongoing search for clues as to what might be causing problems in ME/CFS.
MEA Personal: Facing up to Mental Health Challenges | 11 July 2019 Read More »
We’ve been talking about mental health on social media. Russell explains how he’s faced up to these challenges over the years.
Advances in Understanding the Pathophysiology of ME/CFS | 08 July 2019 Read More »
When does an illness become a disease? Dr Komaroff explores what we know about the biological abnormalities in ME/CFS.
The Emotional Impact of a Long-term Physical Illness by Anna Redshaw | 08 July 2019 Read More »
“No human being can endure what we endure as M.E. sufferers and come away unscathed.”
ME Association June Summary of ME/CFS Published Research | 05 July 2019 Read More »
We’ve updated our central Research Index and feature 17 ME/CFS research studies from June 2019.
ME Association May Summary of ME/CFS Published Research | 19 June 2019 Read More »
We’ve updated our central Research Index and feature 23 ME/CFS research studies from May 2019.
“I strongly believe that if I’d received different treatment from doctors, I would not be as ill as I am today,” Jennifer Chittick
“This debate helps highlight how existing behavioural approaches and treatments are failing patients.” Carolyn Wilshire.
“I now have no regular social life to speak off and have lost contact with most, if not all, of my friends from my old life.” Gemma Corvalan.
“Living with ME is like waking up with the worst flu and hangover combined you’ve ever had in your life, every single day.” Nicola Ingram.
“A neurologist even said “ME is not a real disease.” The medics made her doubt herself and feel ashamed.” Clare Norton.
“It is time for egos to be put aside, for the science to be listened to, for patients to be listened to and the Hippocratic Oath to be remembered – first, do no harm.” Clare Norton.
ME Association April Summary of ME/CFS Published Research | 01 May 2019 Read More »
We’ve updated our central Research Index and feature 15 ME/CFS research studies from April 2019.
Stanford: Biomarker for Chronic Fatigue Syndrome Identified? | 30 April 2019 Read More »
“We clearly see a difference in the way healthy and chronic fatigue syndrome immune cells process stress.” Dr Ron Davis.
ME Research Summary: Something In The Blood by Simon McGrath | 27 April 2019 Read More »
Four independent groups have now found that a factor in the blood can affect cell metabolism/mitochondria in ME/CFS.
“There is little scientific credibility in the claim that the psycho-behavioural therapies should be primary treatments for this illness.”