ahimsa_pdx,
@ahimsa_pdx@disabled.social avatar

From #MEAction:

"We are excited to announce the kick-off of #MillionsMissing 2024 – our ongoing campaign to Teach ME and Treat ME by educating medical providers across our nation’s hospital systems and medical schools about myalgic encephalomyelitis (ME)."

https://www.meaction.net/2024/05/07/millionsmissing-week-is-here-teachmetreatme-in-action/

See link for upcoming events.

1/3

@mecfs
@longcovid

#MEcfs #LongCovid #TeachMETreatME #MedEd #MedMastodon

ahimsa_pdx,
@ahimsa_pdx@disabled.social avatar

If you can, tell your doctor(s) about the Mayo CME (continuing medical education) for ME/CFS. There's an email template available that has a link to the CME:

https://docs.google.com/document/d/15jJZ3-eHQq0pVsshfK-E0so2ucvrBWAzK8en82Xfnfo/edit

I sent this info to my doctor using the messaging system (MyChart) that our clinic uses for communication.

2/3

@mecfs @longcovid

ahimsa_pdx,
@ahimsa_pdx@disabled.social avatar

This toolkit from lists all the different "Show Up From Home" actions that you can do:

https://docs.google.com/document/d/163DeV93SRYNm7Aq2zC_uoaU7NIJmmydaJIi4BQDQDew/edit#heading=h.vyt35j7pvgd3

And here's a link for anyone reading this who wonders, "What is ME/CFS?"

Roughly half of Long Covid patients meet the ME/CFS diagnostic criteria.

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

3/3

@mecfs @longcovid

ahimsa_pdx,
@ahimsa_pdx@disabled.social avatar

Here's a bonus post for this thread because I wanted to post this screenshot with a selfie of Jaime Seltzer! 😁💪

@mecfs @longcovid

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