Please note that I can't provide any information on MCAS doctors. If you're looking for an MCAS specialist, I'd recommend that you join some MCAS Facebook groups and search/ask for recommendations. If you're based in the UK, you could maybe also contact the charity, Mast Cell Action for guidance. Hope this helps!

June is International Mast Cell Disease Awareness Month so I thought I'd make a video on my experience of Mast Cell Activation Syndrome. I've tried to keep things very brief in this video as there's just so much I could share with you, but I'll maybe make some more videos on MCAS as time goes on.

If you also have MCAS, you have my every sympathy and I'd love to hear about your experience of the condition too.

For more information on MCAS, visit Mast Cell Action at https://www.mastcellaction.org/ and they're also on YouTube at    / @mastcellaction  

There are other great resource sites about mast cell disorders including:
Naughty Little Mast Cells: https://www.naughtylittlemastcells.com/
Mast Attack: https://www.mastattack.org/
Mast Cell 360: https://mastcell360.com/


☆ ☆ ☆


Other videos you might be interested in:

I Was Diagnosed as Autistic at Nearly 50 (My First Video!)
   • An Autism Diagnosis At Nearly 50 (My ...  

10 Reasons Why I Thought I Was Autistic
   • 10 Reasons Why I Thought I Was Autist...  

"I Think I'm Autistic, What Do I Do?" Thoughts From a Late Diagnosed Autistic    • “I Think I’m Autistic, What Do I Do?”...  


☆ ☆ ☆


Donations in support of Creative Autistic are very welcome at https://kofi.com/creativeautistic thank you!

#mcas #mastcellactivationsyndrome #actuallyautistic