A mostly German team, "Division of Pulmonary Medicine at University Hospital Münster" Forum thread on that study by the same team here: Sustained...
I was given an ACTH test, also probably because the specialist felt he should do one test to show he had tried something. My morning cortisol...
From Clinical Trials Open label, tick No active control arm, not even a wait list group to give some idea about the impact of natural recovery...
Can you elaborate @Suffolkres?
There really wasn't much benefit: Given it was only the global wellbeing assessment that showed any difference, and then only a small benefit...
4.50 "It turns out diagnostic uncertainty is extremely common in medicine. In fact by many standards, half of symptoms are diagnostically...
It's a bit better, but it still doesn't link to a government page that lists specific health conditions that automatically get better treatment....
Yes, it is very easy. And the petition is very straightforward in its request. Up to 2758. This is all of the text that is part of the...
There are some quotes on the following three themes of the qualitative research that might be useful:
It would be a good topic for a study, to refute the idea that people with ME/CFS are high users of medical services (after the initial effort to...
Interesting to read about Fereshteh's background. I had the exact same thought when reading her paper this morning, so Fereshteh's wonder and...
We now have a thread for this petition: New Zealand: 2022 Petition for the NZ government to recognise ME/CFS as a disability - deadline 29 August...
I thought the discussion and conclusion were thoughtfully written, and think they are worth reading. I hope this team will be funded to do...
Looking carefully at cells with an electron microscope seems like a good thing to do. There were a lot of preparatory steps, and with such a...
B12 levels were a good thing to look at in a big fibromyalgia population, but the results aren't very impressive. The symptoms of fatigue, memory...
IACFS/ME 2022 Virtual Medical and Scientific Conference July 27 - 30, 2022 I think the conference was a useful contribution to the ME/CFS...
I think that the data on symptoms collected on the first visit were not all that was used to diagnose someone with ME/CFS. It seems as though...
@SNT Gatchaman, or anyone Associated Myalgic Encephalomyelitis Society Incorporated Is that ANZMES or another organisation??
Forty-two patients were assessed for eligibility and 32 were randomized. 3 were lost to follow-up, all in the support therapy arm, leaving 17 in...
This quote from the first paper is interesting. My first observation is that treatment is routinely being provided to young people with PNES in...
Separate names with a comma.