Submitted on Thursday 30th May 2019
Published on Friday 28th June 2019
Current status: Closed
Closed: Wednesday 6th November 2019
Signatures: 38
Tagged with
Parliament ~ UK
Debate in Parliament the lack of government funding of medical research for M.E
Myalgic Encephalomyelitis (ME) means "muscle pain plus inflammation of the brain/spinal cord", a chronic neurological illness. *Currently, there is very little funding from the UK government and the responsibility is being left to independent researchers and charities.
Listed by the World Health Organisation as a disorder of the nervous system, ME/CFS affects an estimated 250,000 people in the UK, 17million people across the world. A debilitating illness impacting both patients and caregivers, often going ignored by doctors until the point of crisis. We need to open up the conversation about M.E and stop ignoring those who are unable to campaign for change. It’s our responsibility to give them hope, by signing this petition. #stopignoringM.E
You can't sign this petition because it is now closed. But you can still comment on it here at Repetition.me!
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