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  1. S

    Your OMF gift tripled this week!

    ME does have around 60 symptoms unfortunately....the severe patients can vouch for that. The hope is that what is learned from ME research will benefit fibromyalgia, as they seem similar in some ways. Not sure where Lyme fits in. But right now the focus is M.E and that suits me.
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    Your OMF gift tripled this week!

    There is no guarantee of success, Ron himself has said multiple times science can and does disappoint. They can only promise hard work which I am so grateful for as a severe patient.
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    Your OMF gift tripled this week!

    Totally with you Mattie.
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    USA: National Institutes of Health (NIH) intramural ME/CFS study

    Good luck to that...... it's as slow as molasses. Certainly not counting on them for answers.
  5. S

    Your OMF gift tripled this week!

    I expect good researchers need to get a decent wage!. I think we should all chip in if we can...it's a great opportunity to increase Research funding. Especially after the disappointing drop in NIH funding this year.
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    Stanford Community Symposium 2018: Phair, Metabolic traps, Tryptophan trap

    How does the metabolic trap theory explain the improvement seen in patients receiving ampligen/cyclophosphamide? How does immuno suppression or modulation affect the trytophan pathway...since it's locked into an unhealthy state?
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    Open Seminar about ME in Oslo, Norway Nov. 27th (with amongst other David Tuller)

    Made me giggle...no sugarcoating with our David
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    Machine Learning-assisted Research on ME/CFS

    @mariovitali I hope you are in contact with Dr. Davis
  9. S

    CFS Research Center at Stanford Second Annual Community Symposium Sept. 29-2018

    Is there a general feeling that we are getting closer to answers?
  10. S

    Stuart Murdoch (of Belle and Sebastian)

    I didn't have a good feeling about him from day 1!!!
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    Trial of CT38 for ME/CFS by Cortene Inc.: big claims being made...

    Ah jeez...does anything ever go right in the land of M.E!!!?
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    CFS Research Center at Stanford Second Annual Community Symposium Sept. 29-2018

    Yes but I often think if there was no OMF..we would have very little going on. Fingers crossed it won't take too long to come up with some answers...
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    CFS Research Center at Stanford Second Annual Community Symposium Sept. 29-2018

    Have you guys high expectations of the Symposium? I'm not as excited as last year!
  14. S

    Stuart Murdoch (of Belle and Sebastian)

    Maybe....I know I'm allergic to the term chronic fatigue...and no way wud I ever use it as it's the most feeble description of such a horrible illness.
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    Stuart Murdoch (of Belle and Sebastian)

    Well I wish he would call it M.E then and not chronic Fatigue!!
  16. S

    Stuart Murdoch (of Belle and Sebastian)

    Has he chronic Fatigue or M.E....wish syndrome could at least be added to chronic Fatigue.....as we all know chronic Fatigue is not M.E. I'm not sure about this being a super idea.
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    Hyperintense sensorimotor T1 spin echo MRI is associated with brainstem abnormality in CFS, 2018, Barnden et al

    Are OMF and their Collaborative Centres planning any brain scans does anyone know?
  18. S

    Don Staines and Griffith

    I think I read before that members were wary of Don Staine's research at Griffith University. I couldn't find it here...I got the invest in ME Conference DVD, haven't watched his presentation yet. Don't want false hope...is there a reason their research isn't considered strong?
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