1. Sign our petition calling on Cochrane to withdraw their review of Exercise Therapy for 'CFS'.
    Dismiss Notice
  2. Guest, the 'News in Brief' for the week beginning 21st April 2025 is here.
    Dismiss Notice
  3. Welcome! Read the Core Purpose and Values of our forum.
    Dismiss Notice

Search Results

Search Again
Page 10 of 10
  1. Saz94
    Post

    Is anyone else badly affected by pollen?

    Have you tried Prevalin nasal spray? And sodium cromoglicate eye drops? Prevention stuff like not drying clothes/linen outdoors
    Post by: Saz94, Jun 15, 2019 in forum: Hypersensitivity and Intolerance Reactions
  2. Saz94
    Post

    Is anyone else badly affected by pollen?

    Yes
    Post by: Saz94, Jun 15, 2019 in forum: Hypersensitivity and Intolerance Reactions
  3. Saz94
    Post

    The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread

    Which doctor?
    Post by: Saz94, Jun 12, 2019 in forum: ME/CFS research news
  4. Saz94
    Thread

    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...
    Thread by: Saz94, Jun 7, 2019, 11 replies, in forum: General disability topics and advocacy
  5. Saz94
    Post

    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
    Post by: Saz94, May 27, 2019 in forum: ME/CFS research news
  6. Saz94
    Post

    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....
    Post by: Saz94, May 26, 2019 in forum: ME/CFS research news
  7. Saz94
    Post

    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:...
    Post by: Saz94, May 26, 2019 in forum: ME/CFS research news
  8. Saz94
    Post

    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...
    Post by: Saz94, May 23, 2019 in forum: General ME/CFS news
Find older messages
Showing results 181 to 188 of 188
Search Again
Page 10 of 10