Action Updates

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In reply to

11 hours ago
The opportunity to learn about ME/CFS in the wake of #Covid19 is wholly unique! Not all #longCovid #longhaulers will fit ME/CFS diagnostic criteria. However, it is vital that clinicians who treat & study long-haulers know to make ME/CFS part of their differential diagnosis. #pwME

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In reply to

11 hours ago
Our expert clinicians have seen 1000s of cases of ME/CFS, participated as the consulting clinician on dozens of research projects, & given talks at medical & research conferences. The opportunity to learn from experts of this caliber is rare! #medtwitter
https://t.co/ZCEyqVnaJ7

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#MEAction Network @MEActNet

13 hours ago
#MEAction will host a clinical seminar on treatment & diagnosis of post-viral ME Saturday, August 29, with Dr. Bateman, Dr. Rowe, & Dr. VanNess, followed by a Q&A. This is a unique opportunity and seats are limited, so tell your clinician today! https://t.co/ZCEyqVELAF https://t.co/Ej6iiQiYBB

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In reply to

18 hours ago
3. Make your plan to vote this year! This week is a great time to check on your state’s requirements for the method of voting most accessible to you. Find everything you need to know about voting in your state here: https://t.co/trSW3HfgRT

#pwME #REVUP #NDVRW #CripTheVote

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In reply toAAPD

18 hours ago
2. Encourage others to register! Share this important information with all your fellow people with ME/chronic illness/disabilities to register now! We will be sharing all week on social media so like/retweet/share!

#pwME #MyalgicE #REVUP #DisabilityVote #Spoonie @AAPD https://t.co/OyfPF9bGb3

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