One ME symptom I’ve had since I fell ill is my breathing rate is significantly slower than normal and than I used to breathe before falling ill....
I believe you’ve misunderstood and misinterpreted my main points. I said I don't believe NASH should be getting $35 billion while ME gets next to...
I think you failed to read the full details of this review. A significant percentage of patients across all procedure types required...
You provide zero evidence for that statement. Where’s your evidence that NASH and NAFLD are not predominantly lifestyle diseases? Diseases that...
@NelliePledge please when you have a chance read this article...
Could be. I just want to be clear and I hope I wrote it correctly I do not think obesity is 100% lack of self control. Part genetics, part...
Absolutely, I didn’t say we should spend $0 on NASH, but it’s frustrating that we can’t even get $20 million per year on ME and NASH is going to...
This is the U.S. and for those of us who grew up here we know it’s a very harsh and unforgiving place. You have to be willing to go through hell...
Apologies didn’t mean to judge, tried to make the point that for lifestyle diseases some responsibility should be shared and we should give more...
Again spending billions and billions on lifestyle diseases... and when those who have life destroying disease which is no fault of their own,...
I think I did the already existing poll somewhere, though I thought they shouldve added three more: 11. Almost never, ME improves 12. Almost...
3 days. The ME is creeping back not any sudden return. I wonder if it’s, like I mentioned, the immune system signaling to ramp down as the cold...
@Jenny I just had the same thing, first time since I got ME. For me a bit different I went ME-symptom free for 3 days as my cold started...
I’ve just recovered from the first proper cold I’ve ever gotten since I fell ill with ME/CFS six years ago. The first 3-4 years I never once felt...
Blurring and problems focusing. Gets worse along with my other symptoms when overexerting and PEM builds. I have to stare much harder at computer...
SSRIs have very strong stimulatory effects and make it hard to sleep. I wouldn’t ever use them in ME/CFS they very likely will not work and...
I wouldn’t worry. There isn’t a paper yet, this is just an oral or poster abstract that they’d submitted for the annual ASH conference happening...
I agree ESR isnt a good biomarker for ME Like others here while I had very low ESR early in the disease like 0-2 (and it was measure multiple...
It’s the only one I have in the medicine cabinet :laugh: I thought maybe next time I get the pre-crash symptoms incl. my brain on fire and...
What are your thoughts on naproxen compared to ibuprofen?
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