Is there a link to these? I’m interested because I think Ron Davis has also said that in the severe patient population from the study they did,...
“MRI of the Brain MRI scans of the brain were offered to all participants. MRIs were conducted in different labs and included T1- or T2-weighted...
I was more referring to the fact that the radiologist could be blinded as to who the person was and also, whether or not they had ME/CFS or were...
I think the point of the blinding is that bias could have an effect on how the scans are read by a radiologist, and the measurements that are taken.
Thanks. Earlier in this thread based on your pre print there’s been a few pages of discussion. I was wondering whether you plan to do a study...
I’m confused Is this the same paper that’s been discussed earlier in this thread? That was published in 2019?
I agree Tia. I can see also why patients find that it makes sense. I also developed intolerances / allergy symptoms a few years into ME. But they...
Jen Brea herself knows that the research isn’t there, but is still ok with it: [MEDIA] I think this is the worst thing. But in any case, it’s...
Thank you for your reply in the thread. Please don’t feel any rush to reply or even to reply if you can’t but just writing my thoughts down. I...
It’s interesting you say this because this is what I was thinking too, from reading about it. But I don’t want to dismiss people who are having...
What is the proof that ME or even the CCI she describes is “mast cell mediated”? I always meant to start a thread on MCAS but never got round to...
Yes - here https://www.s4me.info/threads/video-science-for-me-q-a-with-dr-michael-vanelzakker-oct-2019.11791/ michiel tack has posted a summary...
Dr Van Elzakker seemed to completely change his mind later on, in another talk (I think it was the one hosted by Andy from this forum).
And that’s just the official cases. I think ONS shows numbers are holding steady at around 4,000 new cases a day. (28,000 new cases a week).
This might explain why.. famotidine is being bought up by people as it is being looked at as a possible treatment for Covid! It looks like this...
Just an update, Ranitidine is not currently available over the counter in the U.K., as far as I can see, and is still withdrawn. I asked my GP to...
From what I know, 200-400mg is a daily dose for lupus, depending on body weight. 400mg (I think) once a week is or used to be used as a...
This really worries me as I’m due to go into hospital soon and I’m taking double dose PPIs (twice a day). I was thinking of reducing it to once a...
Yes me too. It gets so overwhelming and particularly when I talk to people, “I can’t, I’m too tired”, “I’m too tired to brush my teeth”, “I’m too...
@Mij just a quick note.. you keep referring to me (Lunarainbows) but it’s actually someone else with a similar-ish username, @lunarswirls :p
Separate names with a comma.
