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#MEAction Network @MEActNet

4 hours ago
Can studying #LongCOVID lead to a breakthrough in #MEcfs research? Don't miss @sjmnotes new article! "Several ME/CFS researchers.. have said that the epidemic of long covid provides the perfect opportunity to study that illness & potentially also ME/CFS." https://t.co/jRxTsu2ubh

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#MEAction Network @MEActNet

1 day ago
Reminder #Caregiver #Carer of #pwME meeting is tomorrow- Saturday at 12 pm PT/ 3 pm ET/ 8 pm BST.

Spread the word! #MyalgicE #Support https://t.co/zFOOX9P68a

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In reply to

1 day ago
Learn more about the symptoms of ME/CFS: https://t.co/XIA0ZwDUzF

If you think you may be developing symptoms of ME/CFS after #COVID19 infection, join this new group where long haulers can share their experiences & receive support from #MEcfs patients: https://t.co/CzOsocAM2K

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In reply toJD Davids

1 day ago
"When seeing a doctor about persistent COVID-19 symptoms it may help to come prepared with documents describing your medical history, timeline of COVID-19 symptoms and the top questions you have for them" recommends @TheCrankyQueer. #COVID19 #LongHaulers #LongCOVID

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In reply toJD Davids

1 day ago
. @TheCrankyQueer a long-time advocate for people with chronic health conditions like HIV/AIDS & ME/CFS & #MEAction board member said that the lack of support #LongHaulers face reflects a historic trend in how health care providers treat those with chronic conditions.

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