#ThereForME

#ThereForME

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Why my Long Covid videos resonated
The power of feeling seen
 • Emma Gore-Lloyd
What does the future hold for Forward ME?
An interview with Carolyn Leary, the newly appointed chair of Forward ME
 • Karen Hargrave
The case for change for people with ME — and how to get involved
A guest post from Tessa Munt MP
 • Karen Hargrave
Why is Continuing Healthcare funding so hard to access for people with very severe ME?
Reflections from a year-long battle with the NHS
 • Karen Hargrave
Action for ME’s 2025 Big Survey
Why large-scale charity surveys are so important for ME research and treatment
 • Karen Hargrave
Still here
An update on the Covid pandemic from across the bridge
 • Yanto Evans
Scotland must step up on ME care and research
An opinion piece from Wendy Chamberlain MP
 • Karen Hargrave
Sensory hell and medical harm
My sister’s experience of very severe ME in the NHS
 • Rosie Barrett
Commissioning an NHS service for very severe ME
Perspectives from carers and clinicians
 • Karen Hargrave
The Tiger Who Came to Tea… and stayed
The severity paradox in ME and Long Covid
 • Long Covid Advocacy
Improving access to healthcare services for people with ME and Long Covid
Patients share their challenges, and the actions needed
 • Karen Hargrave
The importance of understanding rest
How my experience of rest as an athlete clashed with my experience of rest as a patient
 • Oonagh Cousins
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