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 24th March 2025 is here.
    Dismiss Notice
  3. Welcome! Read the Core Purpose and Values of our forum.
    Dismiss Notice

Search Results

Search Again
Page 5 of 5
  1. MerryB
    Post

    Does PEM contribute to POTS?

    For me, my orthostatic intolerance contributes to my PEM, and when I am in PEM my orthostatic intolerance is worse (heart rate more spiky). I...
    Post by: MerryB, Nov 25, 2019 in forum: Orthostatic intolerance
  2. MerryB
    Post

    Identification of actin network proteins, talin-1 and filamin-A, in circulating extracellular vesicles as blood biomarkers...ME/CFS 2019, Eguchi et al

    https://www.sciencedirect.com/science/article/pii/S0889159119307627
    Post by: MerryB, Nov 21, 2019 in forum: ME/CFS research
  3. MerryB
    Post

    Identification of actin network proteins, talin-1 and filamin-A, in circulating extracellular vesicles as blood biomarkers...ME/CFS 2019, Eguchi et al

    The full paper is up now - just read it!
    Post by: MerryB, Nov 21, 2019 in forum: ME/CFS research
  4. MerryB
    Post

    M.E. As a runner & HR findings.

    Hi, I know this post is from a while ago but just wanted to say that I notice similar patterns in my HR, although I am much less active than you....
    Post by: MerryB, Nov 20, 2019 in forum: Cardiovascular and exercise physiology (CPET)
  5. MerryB
    Post

    Still to open How to make patients who aren't engaged in the patient community aware of studies recruiting?

    Also maybe see if one of those BBC show that focus on new technologies etc. would do a feature? Like 'Click' or ... I want to say Panorama but I'm...
    Post by: MerryB, Nov 20, 2019 in forum: Recruitment into current ME/CFS research studies
  6. MerryB
    Post

    Still to open How to make patients who aren't engaged in the patient community aware of studies recruiting?

    I got recruited into the UK ME/CFS Biobank that way. They asked my GP practice to send a letter out to the patients on their register with an...
    Post by: MerryB, Nov 20, 2019 in forum: Recruitment into current ME/CFS research studies
  7. MerryB
    Post

    A potential S4ME project: What are the basic science facts that ME advocates need to know and understand?

    Thank you for sharing your thoughts. The thing I feel most strongly about, as a patient, is how unethical it is that current treatments (CBT, GET...
    Post by: MerryB, Nov 17, 2019 in forum: Advocacy Projects and Campaigns
  8. MerryB
    Post

    United Kingdom: National Health Service (NHS) news

    I saw this today, in case it is of interest to anyone? It would be good to have representatives from the ME community involved. Get involved in...
    Post by: MerryB, Nov 12, 2019 in forum: News from organisations
  9. MerryB
    Post

    UK: MRC and NIHR announce ME/CFS workshop, November 2019 & ME/CFS Biomedical Partnership FAQ

    Ok, thank you for your reply!
    Post by: MerryB, Nov 9, 2019 in forum: ME/CFS research news
  10. MerryB
    Post

    UK: MRC and NIHR announce ME/CFS workshop, November 2019 & ME/CFS Biomedical Partnership FAQ

    Thank you for this - I was wondering about whether it would be useful to include relatives who both/all have ME to see whether they all have the...
    Post by: MerryB, Nov 9, 2019 in forum: ME/CFS research news
Find older messages
Showing results 81 to 90 of 90
Search Again
Page 5 of 5