Hypophosphatasia is a condition with high vitamin B6 levels. Its symptoms overlap with fibromyalgia and, to some extent, ME/CFS. If you have low...
I think so
We have heard that a journalist is writing a story about the petition, although so far they have only wanted to speak with doctors, and not the...
That's a bit exciting @Deanne NZ, a consultant interested in ME/CFS. He's a nephrologist who is willing to take referrals for ME/CFS patients, he...
https://www.healthpoint.co.nz/private/specialist/dr-kannaiyan-rabindranath/ Nephrologist welcoming referrals for patients with ME/CFS. I am an UK...
For sure
Anyway, I came here to evaluate Putrino's recent comment that Long Covid in women is characterised by low testosterone. The findings of this...
Milo, you definitely made sense. My objection was to the rigid characterisation of mild ME/CFS people being able to participate in social life,...
That's as dense a collection of unevidenced statements as I have seen for quite some time, even counting the output of the BPS proponents. I am...
Thank you @forestglip for telling us about these software options. We have collectively drafted quite a lot of content on the forum using our...
New petition update On Cochrane's excuses for scrapping the replacement review process they set up: Part 1 5 Jan 2025 People following this...
I started quoting all the very bad bits, but got only to the end of the Background in the Abstract and realised that I had quoted pretty much all...
An interesting study. Possibly the study was underpowered to identify any impact of hormone use (specifically female hormones). Note the lack of...
Thank you so much @butter. I think S4ME could be very effective at fundraising, and I too would love to see the combined wisdom of the forum...
What if we had a thread for members to nominate resources they would like to have available, whether that is a guide on 'Pacing', information on...
The forum committee, both as a committee and as individuals, has suggested to researchers that we could provide private forums and nominate...
Some of us in the S4ME committee have been thinking about creating a website with the forum embedded in it, with pages for resources, things like...
An off-topic discussion has been moved to a new thread: How can we improve the quality of ME/CFS research and clinical care?
I have finally read the paper and I want to have one more go at defending the authors. There is good intent here and also a lot of good content....
Comparison of Clinical and Pathophysiological Characteristics of ME/CFS and Chronic Fatigue Associated with Post-COVID-19 Syndrome, 2024, RIABKOVA...
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