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Wessely & Smith (2015): "Linking benefits to treatment is unethical and probably illegal"
I just came across this, from 2015: https://www.theguardian.com/commentisfree/2015/jul/29/coercing-people-mental-health-problems-work-treatment Which I completely agree with, but was surprised to see Wessely saying it. Isn't it his sort of work that gets used to refuse benefits to ME/CFS...- Saz94
- Thread
- 2015 benefits treatment wessely
- Replies: 11
- Forum: General disability topics and advocacy
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The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread
Yes my friend has severe gastroparesis caused by HEDS- Saz94
- Post #141
- Forum: ME/CFS research news
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The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread
Jonathan, EDS diagnostics have changed since then. See this document. https://www.google.com/url?sa=t&source=web&rct=j&url=https://ehlers-danlos.com/wp-content/uploads/hEDSvHSD.pdf- Saz94
- Post #119
- Forum: ME/CFS research news
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The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread
g Jonathan, hEDS is not simply hypermobility plus pain and fatigue. The NHS Choices website page on EDS says: "People with hEDS may have: joint hypermobility loose, unstable joints that dislocate easily joint pain and clicking joints extreme tiredness (fatigue) skin that bruises easily...- Saz94
- Post #107
- Forum: ME/CFS research news
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Jen Brea: My ME is in remission
I don't find this plausible as an explanation for Jen's remission/recovery. After her thyroidectomy, her ME got WORSE, as well as experiencing new symptoms (those which alerted her to CCI). After her neurosurgeries, all her symptoms got better. It seems clear to me that her remission is related...- Saz94
- Post #269
- Forum: General ME/CFS news