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    Efficacy of faecal microbiota transplantation for patients with [IBS] in a randomised, double-blind, placebo-controlled study, 2019, El-Salhy et al

    https://www.healthrising.org/blog/2019/04/15/nih-chronic-fatigue-lipkin-davis-prusty-oh/ The NIH ME/CFS Conference II: Lipkin’s Possibilities, Prusty’s Big Idea, Oh’s Search and Ron Davis on ALWAYS Moving Forward by Cort Johnson. Section about Dr Oh's talk:
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    Efficacy of faecal microbiota transplantation for patients with [IBS] in a randomised, double-blind, placebo-controlled study, 2019, El-Salhy et al

    Isn't Lipkin or someone working with Lipkin working on mapping the microbiota to such an extent that it would be possible to tweak FMT to give just the right amount and sort of bacteria a patient would need for M.E.?
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    Drug decreases gut leakiness associated with ulcerative colitis

    M.E. is to my best knowledge often associated with leaky gut. Which is why there's such an emphasis on the gut. But much more promising and measured jak-inhibitors are already in the final stages of testing(upaciditinib, filgotinib). And if I recall correctly, trials on m.e. are already underway...
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    JAK Inhibitor Improves Patient-Reported Outcomes in RA

    I think this is one of the two jak-inhibitors that's supposed to be tested for M.E., filgotinib the other.
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    B12/Folic Acid and D3/K2 Supplementation

    I'm not self-treating but I do get a dose of hydroxocobalamin twice a week IM and it does help with pain and fatigue a bit. It's in no way a miracle-solution though.
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    Trial By Error: Some Good News on Cochrane, David Tuller

    That would be better than just withdrawing, yes. Have it on public record once more that those studies are a pile of crap.
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    Cochrane ME/CFS GET review temporarily withdrawn

    Doesn't matter if it is, I'm proud of the reactions to all the ignorant tweets being put out there lately mainly by psychologists or people with a dog in this fight in another way. There's no namecalling, threats or whatever, comments are just being relayed with simple facts.
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    Cochrane ME/CFS GET review temporarily withdrawn

    Isn't the Reuters thing a SMC release? Didn't the SMC lose a lot of credit over the past year(s)?
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    Insights into myalgic encephalomyelitis/chronic fatigue syndrome phenotypes through comprehensive metabolomics, 2018, Lipkin et al

    Does this make us valuable to the cartels? I'm boarding up my house just in case.
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    UK CFS Patient Rediagnosed with Lyme

    There is evidence of in-vitro activity of samento and banderol I think. As to clinical evidence I don't know. Then you have Bühner's protocol, who does seem or atleast claim to use documented treatments with herbs, but the finer details of that and the efficacy-rate of that eludes me.
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    We need new kinds of antidepressants, in addition to pills

    Like fatigue I think it can be a symptom of many things. Rough times or physical failings. Me, I get depressed when I don't stick to my diet which probably has to do with my leaky gut. Being on anti-depressants doesn't help that, staying away from certain foods(especially sugar) does. Drug...
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    UK CMRC 2018 Conference held September 19 & 20 at Bristol

    Actually looks pretty good I think?
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    BBC News: MP Carol Monaghan leads campaign for new ME treatment

    Does seem like she's doing her best and it would be good for our organisations to build a good rapport with her.
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    UK 21 June 2018 | 3-hour ME debate in Westminster Hall, secured by Carol Monaghan

    To be honest, i'm not even offended by that joke.
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    Michael Sharpe skewered by @JohntheJack on Twitter

    Think you got a point there. Destroying PACE is very positive for us and very negative for him. That's where we once again are at a stand-off. The one person's positive is the other's negative.
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    Michael Sharpe skewered by @JohntheJack on Twitter

    It so happens that defending patients and attacking that piece of garbage from 2011 happen to coincide.
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    Michael Sharpe skewered by @JohntheJack on Twitter

    I honestly would just nail him on that. Such and such have given me GET and I got worse, are they to blame or is the therapy itself to blame?
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