#ThereForME

#ThereForME

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Community voices

Scotland must step up on ME care and research
An opinion piece from Wendy Chamberlain MP
Nov 4 • 
Karen Hargrave
Sensory hell and medical harm
My sister’s experience of very severe ME in the NHS
Oct 21 • 
Rosie Barrett
Commissioning an NHS service for very severe ME
Perspectives from carers and clinicians
Sep 23 • 
Karen Hargrave
The Tiger Who Came to Tea… and stayed
The severity paradox in ME and Long Covid
Jul 8 • 
Long Covid Advocacy
Improving access to healthcare services for people with ME and Long Covid
Patients share their challenges, and the actions needed
Jun 24 • 
Karen Hargrave
The importance of understanding rest
How my experience of rest as an athlete clashed with my experience of rest as a patient
Jun 10 • 
Oonagh Cousins
An A to Z of becoming a carer
An alphabetical perspective
May 27 • 
Emma Gore-Lloyd
ME in the family
A generational Sword of Damocles
Apr 29 • 
Jonah Weisz
Research holds the key
Reflections from a 23-year diagnostic odyssey
Apr 15 • 
Karen Hargrave
The hermeneutical injustice of ME
Why the right words don’t exist, and how we can find them
Apr 1 • 
Ella Barnard
Probing an inconvenient truth
Reflections from the Covid-19 Inquiry
Mar 18 • 
Karen Hargrave
Stuck at the bottom of a well
Me, very severe ME and the NHS
Mar 4 • 
Nick Benton
© 2025 Karen Hargrave
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