“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
A life cut short by medical neglect: interview with Sarah Boothby, whose daughter Maeve died at 27 of…
You are being invited to take part in a research study to develop a clinical assessment toolkit for…
Dialogues for a neglected illness – or Dialogues for ME/CFS is a new project being made with an award from the…
Why is this important? The Government has chosen to ‘focus on new claimants’ by providing an extra £20…
This is a radio podcast on Post Covid Syndrome that was broadcast yesterday. It is very good and…
A current problem regarding Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is the large proportion of doctors that are either…