faithie
@faithie.bsky.social
SevereME/vax injured. Can't read, write, watch, walk or talk much. Just me, my bed & my swollen brain. Trying to stay sane. Roy Kent is my spirit animal.
Reposted by faithie
A reminder about #longcovidkids: they won’t present to you like #LongCovid adults, which is why cases are being wildly underreported with shaky science. Our kids deserve better. Thanks Mary Van Beusekom for covering this important topic. www.cidrap.umn.edu/covid-19/not...
October 10, 2023 at 8:48 PM
A reminder about #longcovidkids: they won’t present to you like #LongCovid adults, which is why cases are being wildly underreported with shaky science. Our kids deserve better. Thanks Mary Van Beusekom for covering this important topic. www.cidrap.umn.edu/covid-19/not...
Reposted by faithie
Concise clinical reviews are also a way to offer CME credit. Medical providers can take the free CME by reading the paper carefully and then answering the case-based questions that follow. #MedEd (3/) www.mayoclinicproceedings.org/article/S002...
www.mayoclinicproceedings.org
October 7, 2023 at 4:05 PM
Concise clinical reviews are also a way to offer CME credit. Medical providers can take the free CME by reading the paper carefully and then answering the case-based questions that follow. #MedEd (3/) www.mayoclinicproceedings.org/article/S002...
Reposted by faithie
So nice to see so many community members have found us here already! For anyone new to us- we are #MEAction, a US-based non-profit, igniting a global revolution in ME care.
ME= myalgic encephalomyelitis aka ME/CFS
Learn more at meaction.net.
#pwME #MECFS #MyalgicEncephalomyelitis #LongCovid
ME= myalgic encephalomyelitis aka ME/CFS
Learn more at meaction.net.
#pwME #MECFS #MyalgicEncephalomyelitis #LongCovid
Home
we’re IGNITING A GLOBAL REVOLUTION IN ME CARE Our movement fights for recognition, education, and research so that, one day, all people with ME and CFS will have support and access to compassionate ...
meaction.net
October 7, 2023 at 11:09 PM
So nice to see so many community members have found us here already! For anyone new to us- we are #MEAction, a US-based non-profit, igniting a global revolution in ME care.
ME= myalgic encephalomyelitis aka ME/CFS
Learn more at meaction.net.
#pwME #MECFS #MyalgicEncephalomyelitis #LongCovid
ME= myalgic encephalomyelitis aka ME/CFS
Learn more at meaction.net.
#pwME #MECFS #MyalgicEncephalomyelitis #LongCovid
Reposted by faithie
LSHTM CureME's Dr Eliana Lacerda & UCL's Prof Geraldine Cambridge have been awarded funding by ME Research UK
to investigate ME/CFS immune responses.
Their work will use samples from the ME/CFS Biobank.
www.meresearch.org.uk/research/lac...
to investigate ME/CFS immune responses.
Their work will use samples from the ME/CFS Biobank.
www.meresearch.org.uk/research/lac...
October 6, 2023 at 3:23 PM
LSHTM CureME's Dr Eliana Lacerda & UCL's Prof Geraldine Cambridge have been awarded funding by ME Research UK
to investigate ME/CFS immune responses.
Their work will use samples from the ME/CFS Biobank.
www.meresearch.org.uk/research/lac...
to investigate ME/CFS immune responses.
Their work will use samples from the ME/CFS Biobank.
www.meresearch.org.uk/research/lac...