I am one of the 250,000 people in the UK suffering with CFS/ME.
The 2007 NICE guidelines need a full revision. Suggestions from these guidelines have reported to worsen the condition.
On top of this many parts of the UK do not even have a local hospital-based specialist in which GPs can refer them to.
A lot more funding for biomedical research is desperately needed from the government and shouldn’t be left largely to the charity sector.
Please help us to get the help that we so desperately need.
#NotJustFatigue Video Series: Interview with Creator Elizabeth Ansell
January 13, 2025
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Over the past year, the #NotJustFatigue website, created by Elizabeth Ansell, releases a 10-part, documentary style, short form video series on different aspects involved in living with ME. Titles of the videos include topics such as: You Have No Idea How Serious This Is, Nobody Believes ME, and It’s Not Hysteria: It’s Sexism. In these
