"I talk to my sister. Her personal experience of ME really helps, and she coaches with practical management of chronic fatigue." What? His sister...
Yes! This resonates with my family's experience - we're now up to 6 people with ME among my siblings & my children. And another key related...
This may be beside the point but I am truly amazed that after a mere 6 months Garner "wondered if he would ever get better". I may be a bit...
And I wonder if we might learn something about ME through the screening?
I'd love to read this. Has anyone found it available in Canada or the US? Shipping from the UK tends to be a bit steep.
Done
A wonderfully written piece @Michelle . Loved it.
I concur that it's difficult to diagnose ME if there's another diagnosis that has overlapping symptoms but has a reliable test. A member of my...
Oh for a biomarker!
Thanks @Wyva The article explains what the ME/CFS community has been trying to shout since the beginning of the Covid-19 epidemic. This! While...
Looks like he got a second wind in 2020
My impression was the article had some excellent parts but also a lot about the success of simple breath works as a treatment. Not sure what to...
That's wonderful. I'm very happy about that!
I'm wondering if there's any thought of S4ME joining the "Long Covid Alliance"? So much knowledge to offer.
Here's what I hear from Ron's presentation in the panel. They're working on developing a new technology which can be easily and inexpensively...
I posted this on the thread "A nanoelectronics blood-based diagnostic marker for ME/CFS ....." as it clarifies a point we've been discussing but...
Here's a panel discussion with Ron Davis, Ami Mac & Michael Snyder titled "The Crisis: Post Covid Symptoms with Stanford University" that speaks...
Yes, he had made some improvement but remained very sick at the end of the book. In that case it wouldn't be required reading but never-the-less...
I'm embarrassed he's Canadian.
Excellent. Glad it worked out.
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