Debate in Parliament the lack of an effective policy for the treatment of M.E.

Myalgic Encephalomyelitis (ME) means "muscle pain plus inflammation of the brain/spinal cord", a chronic neurological illness, but "the majority of patients presenting with symptoms of ME in the UK are still referred to psychotherapists for treatment" (Dr Ian Gibson). A policy review is overdue.

This petition closed on 13 Mar 2018 with 5,705 signatures


Reticulating Splines

You may be interested in these active petitions

1. Provide funds from Proceeds of Crime Act to police charities and not-for-profits - 4,711 signatures
2. Remove powers to vary income tax rates from the Scottish Parliament - 8,478 signatures
3. Home fee status for BN(O) students after 3 years continuous stay in the UK - 14,680 signatures
4. Increase funding for treatment and research into endometriosis - 7,657 signatures
5. Hold a Public Inquiry into the shortage of ADHD medication - 3,065 signatures

The NHS provides psychiatric therapies for what it refers to as "CFS/ME". These therapies are often ineffective and sometimes make patients worse. They are the result of a Myalgic Encephalomyelitis policy heavily influenced by psychiatrists who are skeptical about the existence of Myalgic Encephalomyelitis. It is time for a policy re-think about the effectiveness (and cost-effectiveness) of current treatment.
See: http://www.tymestrust.org (for the effect of current policy on children with ME).


Petition Signatures over time

Constituency Data

Reticulating Splines