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“It feels like you are a few days from death.”
Community Voices: Beth Dobbin’s BBC interview
Oct 20
•
Emma Gore-Lloyd
41
1
15
"Rationing care affects lives"
Three contributors with ME and Long Covid share their experiences of navigating social care assessments and support
Aug 18
•
Karen Hargrave
47
4
12
How many people in the UK are affected by ME?
We have a data problem
Jul 21
•
Emma Gore-Lloyd
54
24
18
Why my Long Covid videos resonated
The power of feeling seen
Jun 23
•
Emma Gore-Lloyd
13
2
What does the future hold for Forward ME?
An interview with Carolyn Leary, the newly appointed chair of Forward ME
May 26
•
Karen Hargrave
32
6
4
The case for change for people with ME — and how to get involved
A guest post from Tessa Munt MP
Mar 4
•
Karen Hargrave
39
4
8
Why is Continuing Healthcare funding so hard to access for people with very severe ME?
Reflections from a year-long battle with the NHS
Feb 10
•
Karen Hargrave
48
12
7
Action for ME’s 2025 Big Survey
Why large-scale charity surveys are so important for ME research and treatment
Jan 13
•
Karen Hargrave
29
2
8
Still here
An update on the Covid pandemic from across the bridge
Nov 18, 2025
•
Still Here
16
3
3
Scotland must step up on ME care and research
An opinion piece from Wendy Chamberlain MP
Nov 4, 2025
•
Karen Hargrave
24
4
3
Sensory hell and medical harm
My sister’s experience of very severe ME in the NHS
Oct 21, 2025
•
Rosie Barrett
46
6
7
Commissioning an NHS service for very severe ME
Perspectives from carers and clinicians
Sep 23, 2025
•
Karen Hargrave
33
5
4
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