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
#MEAction Network
ME/CFS community! Please, if you are able, come to the community meeting held by #MEAction on tomorrow - Sunday, June 14 at 3 PM ET. We are facing a changed advocacy environment, and to make any progress, we have to forge new paths and move forward together. Come tomorrow and see where we stand.
REMINDER! Join us for a community meeting TOMORROW - June 14th at 3 pm ET to hear about the next steps #MEAction is taking in US advocacy, and what steps you can take to be part of these efforts. https://ow.ly/p1jM50ZablP
#PwME #MillionsMissing #FrailAndFurious #MyalgicEncephalomyelitis #MECFS
Karen Gordon bravely took part in our video that lit up London for the very severely ill and now she needs your help.
#MEAction Network
Miranda shares her experience as a #pwME & shares her advocacy within the disability and unhoused community at #MillionsMissing. Miranda goes on to explain that #Medicaid is the main pathway to get home care and home care is the main pathway to safety.
https://youtu.be/sn6RWKmnT3Q
