Also worth noting, Brown says He admits it's a flawed paper whose author was decietful to the point of making them rewrite portions of the...
I really think McGregor is keyed into something. I don't know what that something is, but I resonate with virtually every thing he's writing and...
It would be difficult but I think this is a challenge with clear parameters and a clear objective, and people are much more likely to participate...
I like this thread, but maybe it belongs in symptoms not news?
Cort has an article on Nimotop today. I was able to try a dosage of 30 mg for a couple weeks years ago. I stuck to just once a day looking for the...
>They told me to Meditate. Then the speaker sang... No fucking joke, she sang a song... To the tune of The Way We Were -- telling us to pace...
Maybe the SMC should send someone over? I mean, they are really interested in the truth and not pushing their client's agendas, so I can't imagine...
Yes, sorry, that's what the esophogram was, modified barium swallow, but it only showed mildy delayed passage of hard food. Also had nerve...
About 7 years ago I had my c3b levels tested. They were 14 x the max of the normal range. I have no idea what that means, if that's significantly...
I'm sorry you took a different perspective as an accusation. I believe the argument of why the assumption can't be made is clear in my post. There...
Do you attribute this to IVIG?
Idk if Jennie Spotila is on here, but if she is - thank you, you do a GREAT service for the ME/CFS community. Your blogs are important.
Have listened to the whole thing now. She seems to key in on 3 possible sub-groups. Obviously it's a very small pilot study. But the patients with...
Interesting that AMPD3 gene was flagged (frequency of 6% in population, 50% in pwme (10)). She mentions...
I was just asking hypothetical, a question that I asked myself as I was reading this thread.
But, if you had Chiari, would you? Just a thought experiment. Because one could make the same argument Chiari and ME/CFS don't look a lot alike....
It is usefulness to ask whether, in general, persons with ME/CFS have symptoms consistent, in general, with people with CCI. And the pathological...
It's possible he didn't have ALS but another motor neuron disease or perhaps a MND sub-type so rare only he had - that is after all how rare some...
I'm pretty sure all that needs to be asked at this point is two related questions. 1) Can CCI produce the symptoms of ME/CFS? and 2) Do ME/CFS...
Would getting the NIH study to check for CCI also help? They would have a more neutral perspective and a healthy cohort. Because I’m not sure how...
Separate names with a comma.
