#MEAction Network
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
- We are winding down our day of #MillionsMissing action but just starting a week focused on creating change! WOW! You are blowing us away with the amazing shares on social media and we are beyond grateful to all who showed up in person in DC and at actions around the world. #DisabilitySOS
- Kim Moy shares why she is protesting today for #MillionsMissing. Please TAKE ACTION to help the #MIllionsMissing. Sign the letter to the NIH, call your congressperson, share our stories, and/or donate to #MEAction to continue our work! www.meactions.org/millionsmiss... youtube.com/shorts/e_ZOG...
- Thanks for sending out your SOS signal today, @naomidharvey.bsky.social !
- Call Congress to let your Members know the #MillionsMissing were outside their door today! Ask your Members to oppose Medicaid cuts & not force desperately ill people to work to keep their healthcare. Urge Congress to support ME/CFS Research. Call Script: bit.ly/44uSkxJ #DisabilitySOS #Medicaid
- Join us TODAY for #MillionsMissing! Ben shares that this is an SOS moment for Medicaid. "Let's fight like hell to save Medicaid." Join us in DC at Upper Senate Park at noon ET or via livestream & ALL DAY online. millionsmissing.org. #ProtectMedicaid #DisabilitySOS #Medicaid #pwME #MECFS
- Today is #MillionsMissing! #MEAction is organizing today’s protest to call on officials to protect the basic infrastructures that support our communities: Medicaid, home care support, research funding and open science. We are sending out a #DisabilitySOS! www.meactions.org/millionsmiss...
- Forcing chronically ill Americans to work to save their healthcare will harm millions with #MECFS and #LongCOVID, especially those who are newly sick and whose only hope for recovery is rest! #MEAction is protesting #Medicaid cuts TOMORROW at Capitol: bit.ly/3RWrcQL Press email: press@meaction.net
- We miss our co-founder Beth Mazur. We have lost too many and that loss is carved into our souls. We are honored to carry them with us. Board member & her brother, Steve Mazur, shared his SOS for #MillionsMissing. "I am here for my sister and sending out an SOS for ME." millionsmissing.org
- Most of our community are not well enough to protest on the street but we are making our voices heard from our beds about why cuts to ME/CFS research funding is so devastating to our community. Wilhelmina Jenkins is one of the #MillionsMissing showing up from home! youtube.com/shorts/ypEHp...
- Reposted by #MEAction NetworkPlease sign. ME is underfunded. The Research Roadmap has been designed and needs funding to progress. Many with Long Covid have benefited from ME advocacy and can help support ME patients by signing.
- We are fighting for funding for the ME/CFS Research Roadmap. We have a letter urging Dr. Bhattacharya to allocate $50 million to fund the ME/CFS Research Roadmap. Sign our new letter now: bit.ly/MEcfsRoadmap The more signatures we gather, the louder our call for action. #PwME #MECFS #NIH
