#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
24,24K Tweet
20,20K Followers
2,2K Following
Register for our Sept. 10 webinar with Dr. Peter Rowe (Johns Hopkins Children's Center) to discuss his book "Living Well with #OrthostaticIntolerance: A Guide to Diagnosis & Treatment." He'll cover causes, symptom mgmt & answer your questions. #MECFS #LongCovid. ow.ly/XQm450SKnKf
Sending out our best to all who are attending the #MECFS Collaborative Research Center Working Group Meeting at Stanford Med/SGTC this week including #MEAction's Scientific Director Jaime Seltzer It'sME(Jaime). The meeting is closed because unpublished data is being presented.
ANNOUNCEMENT: The Emory University School of Nursing in partnership w/ CDC will host a Voice of the Patient panel discussion on September 18. MEAction GA advocates will talk about their lived-experience with #MECFS and #LongCovid. If you're in ATL, join us! #TeachMETreatME
Can the ME Community help ME Foggy Dog get more signatures on this petition and get it trending during ME Awareness hour this evening? ow.ly/3yKp50TfbNS #MyalgicEncephalomyelitis #VerySevereME #SevereME