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$14,701 raised, 21% of total, 110 donors 23 days left. https://crowdfund.berkeley.edu/project/43450

$11,796 raised, 17% of total. 98 Donors 24 days left https://crowdfund.berkeley.edu/project/43450

I can't answer because I became ill in 1995 and was concentating too hard on trying (unsuccessfully) to find my disappeared cat to think of myself much.

$4,020 raised, 6% of $67,000 Goal 54 Donors https://crowdfund.berkeley.edu/project/43450

$2,900 raised so far, 4% of total https://crowdfund.berkeley.edu/project/43450

Do you know who wrote that?

Looks interesting from a quick look, but I'm rather puzzled by the reference at the end to 'United States Association for Body Psychotherapy'. Also supported by the Chaja Foundation. ???

I don't get much muscle pain, but otherwise I am similar to you - very rarely need to lie down. I don't think I have orthostatic intolerance. My legs get tired below the knees. I also have difficulty standing still - have to keep moving my weight from one leg to the other, so queues are a...

Merged thread BBC Radio 4 programme featuring 'Functional Neurological Disorder' (FND) I haven't listened to this yet, but can be fairly confident that it will be a load of cr*p, knowing Claudia Hammond's views/approach: "All in the Mind FND - the most common disorder you’ve probably never...

"Melanie Phillips’s intelligent article" Really? Is that the Melanie Phillips whose extreme, often-garbled nonsense used to feature on Radio 4's Moral Maze? I don't know if it still does, as I gave up listening years ago largely due to her.

I had no idea what moxibustion was, so looked it up: https://en.wikipedia.org/wiki/Moxibustion

I was fine with morphine which I took (illegally) for agonising wisdom tooth pain which the official doctors wouldn't give me anything strong enough for.

I thought that dilatation was widening rather than redness?

I took heroin once and it made me throw up for 8 hours. No pleasure at all, so never tried it again!

This does not make sense: adults who have been diagnosed with ME/CFS and also people with ME/CFS triggered by a covid infection. They are all people with ME/CFS! Also, in the second example it doesn't state whether they need to be adults.

I used to get a lot of tinnitus and deafness, but I think it was due to scratching and trying to clean out my ears with various things. They tended to itch a lot in the summer. Sometimes I went completely deaf until the ears were eventually unblocked. I couldn't even use the phone.

The petition/open letter is here: https://openletter.earth/open-letter-to-the-british-paralympic-association-about-the-need-for-a-caveat-fcfde578

I just listened to the video of the woman who set it up, and am concerned that the only option under "This website uses cookies" is to accept. I didn't accept.

There should be more info on the page.

https://www.bbc.co.uk/news/articles/cy0rwzd0r1do By Lili Sheppard BBC News, Somerset Published 7 hours ago An ex-nurse is attempting to set a new world record by travelling from John O’Groats to Land's End in 45 days using a standard wheelchair. Army veteran Lexi Chambers has fibromyalgia...