Calling all British M.E. sufferers & allies,
Inspired by our American friends and the progress that has been made over in the States with government funding and new research projects, we think it’s time for patients to put the pressure on the UK parliament. We are asking for an increase in budget to fund bio-medical research as well as the formation of a work group to represent the issues facing our community in government.
Although only British citizens or UK residents have the right to sign, we think that with over 250,000 diagnosed M.E. sufferers and many more undiagnosed cases, as well as our families, friends, and M.E. allies, we can hit the 10,000 signature requirement for the government to respond to this petition.
Let’s do this!
Press Release: Cochrane Library Faces Backlash Over ME/CFS Review Cancellation
January 24, 2025 – Cochrane Library has made the shocking decision to abandon an independent analysis of its 2019 review of exercise therapy for myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) – and has altered the date of publication to make the review appear current when, in fact, its sources are 10 years old or
1 thought on “10,000 signatures for more research funding in the UK!”
We need more research! Too many suffering in silence and kept out of work and on benefits. This then causes depression.
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