Sally Burch

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history

Sally Burch is an advocate for people with Myalgic Encephalomyelitis, and a member of the NICE guidelines review panel in the UK, which is due to complete its work in 2020.[1][2]

Sally has been living with Myalgic Encephalomyelitis since 2012, and is opposed to the biopsychosocial model of the illness which currently dominates NHS policy and recommends graded exercise therapy (GET) and cognitive behavioral therapy (CBT) as primary treatments.[2]

Talks and interviews[edit | edit source]

Online presence[edit | edit source]

  • Twitter
  • Facebook
  • Blog
  • YouTube

See also[edit | edit source]

Learn more[edit | edit source]

References[edit | edit source]

  1. ↑ NICE (October 28, 2018). "Committee member list | NICE CG53 CFS/ME guidance update". nice.org.uk. Retrieved October 20, 2018.
  2. ↑ 2.0 2.1 Burch, Sally (May 11, 2018). "Just ME: Trust, in the context of ME". Just ME. Retrieved October 28, 2018.
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