Mastodawn

[email protected]❌👑10h ago

Hello 👋

I need your help! We need as many signatures on this community letter as possible! Anyone in the USA can sign! Allies needed!

Solve ME & #MEAction are asking State Medical Boards to add ME/CFS questions to national licensing exams.

Doctors need to learn about ME/CFS!

Please sign here:

https://docs.google.com/forms/d/e/1FAIpQLSdXIoHN1Ej7qadY4fhGF7BZB8dtX7zWul0jugb4sh75Ybl2RA/viewform

There are a few pages (scroll down to click next) but it doesn't take long.

Boosts appreciated!

Thank you ❤️

#MEcfs #LongCovid #MedMastodon #MedEd #Healthcare

@mecfs
Want to learn more about ME/CFS? (myalgic encephalomyelitis / chronic fatigue syndrome)

Here are a few links.

From #MEAction:

https://www.meaction.net/what-is-me

From Solve ME:

https://solvecfs.org/me-cfs-long-covid/about-the-disease/

From the CDC:

https://www.cdc.gov/me-cfs/about/index.html

Fact sheet from Science for ME forum:

https://www.s4me.info/threads/science-for-me-fact-sheets.43310/#post-596527

#MEcfs #SolveME #Science4ME

WHAT IS M.E.? | #MEAction

ME/CFS is a complex chronic disease that presents with symptoms in multiple body systems, and is considered a neurological disease by the World Health Organization. Learn more here.

#MEAction

@mecfs
Sadly I don't think any of these ME/CFS groups are on Mastodon or other Fediverse platform.

You can read Bluesky posts from #MEAction here:

https://bsky.app/profile/meactnet.bsky.social

You can read Bluesky posts from Solve ME (they post less often) here:

https://bsky.app/profile/solveme.bsky.social

#MEAction Network (@meactnet.bsky.social)

A global network of people empowering one another to fight for equity for myalgic encephalomyelitis. Home of the #MillionsMissing linktr.ee/meactnet #pwME #MyalgicEncephalomyelitis #LongCovid #MECFS #ChronicIllness #DisabilityJustice

Bluesky Social