The Long Hauler Tragedy: More Frightening than Halloween Nightmares
For the past 30 years, still another group has suffered from the trauma of an illness and then…
Scottish Good Practice Statement on ME-CFS
The Scottish Govermnet have provided an email update on implementing undertakings given by the Cabinet Secretary to the…
Myalgic Encephalomyelitis / Chronic Fatigue Syndrome CPD
As an immediately relevant and useful tool for medical professionals and students receiving notice of these updates, it…
“Life in Lockdown: What Matters When All Is Lost”
Thoughtful post by Naomi Whittingham who reflects on living through the lockdown as someone who has effectively had…
Charities request for the removal oF harmful treatments
As charities supporting people with M.E. we have been actively campaigning for NICE to remove the recommendation of…
25% ME Group stance on exercise
We are extremely concerned that some medical/care professionals and sports/exercise specialists are still recommending exercise programmes and/or graded…
Severe ME in Children
A current problem regarding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is the large proportion of doctors that are either…
Could COVID-19 trigger chronic disease in some people?
Could COVID-19 trigger chronic disease in some people? A handful of viruses have been associated with long-term, debilitating…
ICC Definition for M.E.
Myalgic encephalomyelitis is an acquired neurological disease with complex global dysfunctions. Pathological dysregulation of the nervous, immune and…
Health Care Responsibility and Compassion-Visiting the Housebound Patient Severely Affected by ME/CFS
Many people with severe Myalgic Encephalopathy/Chronic Fatigue Syndrome (ME/CFS) commonly receive no care from healthcare professionals, while some…