Good article as always Dave - i would make the small point that comparing the activists in Paris to Kanye West is probably not the best point of comparison considering that in the last few years West has openly claimed to be a Nazi and admire Hitler, sold swastika merch on his website and recorded a song to that effect*. And of course the BPS lot have in the past compared ME/CFS activists to Nazis.Trial By Error: News Bits--"Frail & Furious" for #Millions Missing; Usual Suspects at Psych Confab; Long COVID Advocates Channel ACT UP | Virology Blog
By David Tuller, DrPH *This is a crowdfunding month at UC Berkeley. If you’d like to support my work, the link is here. ********** "Frail and Furi ...virology.ws
i would make the small point that comparing the activists in Paris to Kanye West is probably not the best point of comparison considering that in the last few years West has openly claimed to be a Nazi and admire Hitler, sold swastika merch on his website and recorded a song to that effect*.
www.meaction.net
meassociation.org.uk
alifehidden.com
For ME Awareness Month I made a severe ME body‑bag “dance” film about death within the ME community.
"Medical Frailty" was the key phrase at this year’s #MillionsMissing because it matters in order to truly validate diagnosis and experience, fund research, and protect people with ME from harm.
Our US Action had very clear wins. #MEAction's focus this #MillionsMissing was educating key allies at the HHS about ME - with a focus on protecting Medicaid for ME, Long COVID and other infection-associated diseases.
From a policy perspective, this has been an extremely productive #MillionsMissing. At the HHS event, we were joined by Dr. Stephanie Haridopolos, Acting Chief of Staff and Senior Advisor to the U.S. Surgeon General. Dr. Haridopolos expressed her allyship and recognition of ME as a serious, complex disease. We also met a Center for Medicare and Medicaid Services staffer who was very open to discussions. These are not small. They are clear victories when many obstacles are standing in our way.
#MEAction advocates and staff had a successful series of meetings with 11 Congressional Offices about appropriating funds to the ME/CFS Research Roadmap, many of those in partnership with @NotJustFatigue.
I posted a long thread on Mastodon on May 12. Posting the thread here in case anyone is interested.![]()
I posted a long thread on Mastodon on May 12. Posting the thread here in case anyone is interested.
I‘d like to second that. Very clear, concise, yet informative thread. Thank you!Though it contains so much information, it is structure as lots of short post makes it very accessible.
That's an excellent thread, ahimsa. Thank you for all your work on it.I posted a long thread on Mastodon on May 12. Posting the thread here in case anyone is interested.
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Ahimsa (@ahimsa_pdx@disabled.social)
Attached: 1 image It's May 12th, International ME/CFS Awareness Day Also called World M.E. Day! This thread talks about 4 things: 1. My ME/CFS story (brief) 2. Facts about ME/CFS and Long Covid 3. Helpful resources for patients (and friends/family) 4. Actions you can take to help folks...disabled.social
Just FYI, to see this thread there's no need to log in, no advertisements, and no tracking, cookies, etc. I checked with 2 browser plug-ins — EFF's privacy badger and uBlock origin — and both show 0 trackers.