“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
Campaigners say that each day a health watchdog delays publishing new guidelines on ME “puts more people at…
A. whereas the Committee on Petitions has received several petitions raising concerns over the absence of treatments and…
David Tuller critiques the PACE trial authors for their response to George Monbiot’s column on ME/CFS, accusing them…
We have secured funding for a very large study to analyse DNA from the saliva of people with…
A current problem regarding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is the large proportion of doctors that are either…
There is clear evidence that ME is not the same as depression or any other psychiatric disorder. In…