12 May, International ME Day - Scottish Parliament: 11th May 2017

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Revision as of 19:11, May 11, 2017 by DxCFS (talk | contribs) (Created and Populated Page - Needs Category)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

12 May, International ME Day - Scottish Parliament: 11th May 2017 is a Members' Business segment in Scottish Parliament acknowledging May 12th as "International ME Day". Several members spoke for over 30 minutes about the problems with diagnosing Myalgic Encephalomyelitis (ME), the trivializing name of Chronic Fatigue Syndrome (CFS), health of ME suffers, negative experiences of people with ME/CFS from healthcare professionals and the general public, the incorrect diagnosis of a psychiatric condition and the history of psychiatry misapplied to the disease, the need for better GP care for adolescents and adults and more.

Summary of testimony[edit | edit source]

"That the Parliament acknowledges that 12 May 2017 marks the international awareness day for myalgic encephalomyelitis (ME), which is commonly known as chronic fatigue syndrome; understands that ME is often labelled as a "silent" illness but can bring great mental and physical exhaustion to those living with it; believes that over 20,000 adults and children in Scotland have the condition and that the effects include cognitive impairment, poor short-term memory, muscle and joint pain, gastrointestinal problems and food intolerance; commends the work of the various charities across Scotland and beyond in highlighting the circumstances faced by people with ME, and commends them on the support that they offer."[1]

Parliament TV recording[edit | edit source]

References[edit | edit source]