
#MEAction Network
@meactnet
A global network fighting for equality for Myalgic Encephalomyelitis. #MEAction #MillionsMissing
linktr.ee/meactnet
ID: 2501259470
http://meaction.net 17-05-2014 10:54:10
25,25K Tweet
19,19K Followers
2,2K Following

⁉️📢 Calling those with #LongCOVID who have had a Pemgarda infusion — how did it affect your symptoms compared to your pre-infusion baseline? If you had improvements or worsening, let us know in the comments how long they have lasted. Please share 🙏#pwLC Patient-Led Research Collaborative




The United States Senate’s Budget Reconciliation Bill Threatens the Lives of Disabled Children Elena Hung (she/her)'s statement below 👇 #ProtectMedicaid



🗣️Important wide-ranging interview with high profile Aussie journo‼️Free podcast 🎧 Listen & share 😀 #MyalgicEncephalomyelitis #MECFS #LongCOVID #InvisibleIllness #pwME ME Group Australia (Rachel) ME Advocacy Network Australia (MEANA) Tom Kindlon Eliza Charley | Actress on Pause Solve ME/CFS Initiative #MEAction Network Millions Missing.. MillionsMissingNL



Check out this webinar from our friends at Solve ME/CFS Initiative. The implications of this trial for people with ME/CFS and other IACCIs will be discussed, and attendees with Long Covid will learn more about how to participate. Tuesday, July 22 @ 3 pm PT / 6 pm ET #pwME #LongCovid




The first paper that uses our Pacing Narrative Study data is now published. Thank you to all who participated! Stephanie Grach MD MS is building a case for vocal differences to detect PEM. She found many discussed such issues during a crash. mdpi.com/2077-0383/14/1… #MECFS #pwME


