Mast Cell Activation awareness day.
MCAS varies person to person and what may be okay one day can have a severe effect another.
It may appear as if our triggers are weird, but please don’t shrug them off just because their not “typical”
Since #MCAS and #dysautonomia remission, I’ve started running, but my feet are blistering. Never was a problem on the track team and same across multiple shoes, socks, insoles. Is this an #EDS thing? Hopefully they toughen?
Sign up for CME course on #Lyme Disease- Hosted by @aucott_john & Mark Soloski @HopkinsMedicine. Speakers incl: Kim Lewis (Northeastern) on microbiome, A. Baranchuk (Queens U) on carditis, Peter Rowe (JHU) on ME/CFS, Brian Fallon (Columbia) on neurocognitive & neuropsych impacts
What do you know about Mastocytosis and frequent #migraines? Are the 2 related? How do you manage them?
🔹Join the #Mastocytosis and #MastCells RareConnect community and participate in the discussion. https://t.co/VNuaPBMNqV
I highly recommend this Bendy Bodies episode for great info about #MCAS and how it relates to #EDS and gastrointestinal disorders! #chronicillness#pots@BluesteinLinda https://t.co/0DlimMhw4z
Thank you @ChrisHrapsky for covering Dr. Afrin’s research about #MCAS and #longhaul. MCAS is certainly not rare, but access to diagnostic tests and treatment is https://t.co/nqouQPfIcS