“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 to live through their
own lockdown due to severe ME for decades
Similar Posts
WCA consultation support for organisations
The DWP are proposing to make the WCA much harder to pass and this is going to have…
ME Voices Wales / Lleisiau ME Cymru
WAMES is co-coordinating a series of on-line consultation events for people with ME in Wales called ME Voices…
Severe ME Inquiry
The All-Party Parliamentary Group on ME (APPG) has launched its inquiry into Severe ME. Action for M.E., the…
Myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome: diagnosis and management
This guideline covers diagnosing and managing myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome (ME/CFS) in children, young people and…
#DecodeME Matters
#DecodeME Matters As many of you are aware our advocacy worker, Helen Baxter, has been assisting people with…
Another nail in the coffin of those who claim that ME is psychosomatic
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Organic Disease or Psychosomatic Illness? A Re-Examination of the Royal Free Epidemic of 1955…