“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
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
Special Issue Information Dear Colleagues, “ME/CFS—The Severely and Very Severely Affected” is a proposed themed Special Issue of…
For many years the definition of ME/CFS has been wrongly placed in the medical textbook by Kumar &…
New report on the most serious ME-sick Between 2500 and 5000 ME-sufferers have severe or very serious ME,…
The health department failed to explain the postponement to its long-awaited strategy for treating chronic fatigue syndrome which…
Dr. Byron M. Hyde, a distinguished pioneer in Myalgic Encephalomyelitis (ME) research, passed away on November 17, 2024….
This is the inpatient experience of a patient with very severe ME, whose father Michael Gordon gave an…