“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
NICE GUIDELINES PRESS RELEASE
EMBARGOED UNTIL: 00:01, 29 October 2021 PRESS RELEASE NICE ME/CFS guideline outlines steps for better diagnosis and management…
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…
Norwegian ME Report
New report on the most serious ME-sick Between 2500 and 5000 ME-sufferers have severe or very serious ME,…
Back to the Future? Immunoglobulin Therapy for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
The findings of controlled trials on use of intravenous immunoglobulin G (IV IgG) to treat myalgic encephalomyelitis/chronic fatigue…
Myalgic Encephalomyelitis / Chronic Fatigue Syndrome Announcements
Statement My Rt Hon Friend the Secretary of State for Health and Social Care (Sajid Javid) has made…
