Widley Successful #NeverBetAgainstOccam by Dr. Afrin: https://xitter.cf/t.co/eUor8gyLC1 Information, research & publications on Mast Cell Activation Disorder (#MCAD/#MCAS) & more!
Ijamsville, MD
Joined February 2016
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Mast Cell Research retweeted
October 20 is international Mast Cell Disease Awareness Day… mastocytosis-mcas.org/blog/a…
Mast Cell Research retweeted
🧐”Mechanisms of vitamin D₃ metabolite repression of IgE-dependent mast cell activation”pubmed.ncbi.nlm.nih.gov/2446…
Mast Cell Research retweeted
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”
Mast Cell Research retweeted
Does anyone know of a Dr. in New Mexico who is familiar with Mast Cell Activation Syndrome #MCAS ?
Mast Cell Research retweeted
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?
Mast Cell Research retweeted
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
Are you frustrated that your health practitioners don't know how to diagnose Lyme disease, recognize an EM rash, or acknowledge the seriousness & complexity of "long haul" #Lyme disease?- @HopkinsMedicine is offering a CME on Lyme disease on Friday June 4 hopkinscme.cloud-cme.com/cou…
Mast Cell Research retweeted
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. rareconnect.org/en/community…
Mast Cell Research retweeted
What are my mental tips for living with #MCAS #EDS and #dysautonomia? Check out this podcast episode. #MentalHealthAwarenessMonth podcasts.apple.com/us/podcas…
Mast Cell Research retweeted
I highly recommend this Bendy Bodies episode for great info about #MCAS and how it relates to #EDS and gastrointestinal disorders! #chronicillness #pots @BluesteinLinda podcasts.apple.com/us/podcas…
Mast Cell Research retweeted
As much as I hate to know more people are suffering, I am hoping #MCAS will gain recognition and research funding #longhaul kare11.com/amp/article/news/…
Yes! Awesome interview by @ChrisHrapsky and behind the scenes efforts by the amazing @ashablaketv!
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 hometownsource.com/sun_curre…
Mast Cell Research retweeted
#MCAS symptoms can range in severity from discomfort to disability. Tests and treatment can help. hellsbellsandmastcells.com/w…
