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302 total results
Comments (281)
YES I am 100% sure my SFN started after covid infections. But it started at the...
https://connect.mayoclinic.org/comment/908086/
allergist told me recently that SFN/MCAS
Hugs of sympathy to Frenchie333 for what you have gone through with MCAS. Found out about...
https://connect.mayoclinic.org/comment/748078/
for what you have gone through with MCAS
I’m so sorry this is happening to you. I have small fiber neuropathy as well, believed...
https://connect.mayoclinic.org/comment/907349/
addition to the person you’re seeing for MCAS
I mentioned 23 and Me only because that's the one that came to mind. I think...
https://connect.mayoclinic.org/comment/745440/
mastocytosis which has escalated to MCAS-GI
Do your own research on Mast Cell Activation syndrome…..it’s VERY real. You have a LOT of...
https://connect.mayoclinic.org/comment/1015300/
Anyway the protons on line for MCAS
Hello 👋🏻 I had a regular PET scan March that showed just physical activity in all...
https://connect.mayoclinic.org/comment/756669/
wanted to address the possibility of MCAS
I got my second dose of Moderna 2 days ago and am still in agony. I...
https://connect.mayoclinic.org/comment/598648/
I have 2 autoimmune diseases and MCAS
I had my third covid infection in mid-December of 2022, absolutely the worst of the lot...
https://connect.mayoclinic.org/comment/899871/
What remains is a pitched battle with mcas
Yes extensively ……what I eat is now very curtailed but choking is very much less. I...
https://connect.mayoclinic.org/comment/962860/
acid in it or any histamine brings on MCAS
My A-fib was verrrrrry noticeable. Jumping and fluttering! No heart trouble until the Pfizer double jab....
https://connect.mayoclinic.org/comment/729547/
Then my mastocystosis escalated to MCAS
Thank you so much! I do follow the EDS blog, but I’m new here. I spend...
https://connect.mayoclinic.org/comment/796752/
nutritional deficiencies, as well as MCAS
Hello! Ive been really struggling with coping with my symptoms and diagnosis journey for MCAS. Not...
https://connect.mayoclinic.org/comment/134372/
symptoms and diagnosis journey for MCAS ... allergist who told me that it might be MCAS
lol! I wouldn’t say here in the US it’s acknowledged as different types of LC. This...
https://connect.mayoclinic.org/comment/1176575/
I have MCAS as well so I don’t tolerate
Hi..I’m 72 and have a number of disorders and immunity issues and syndromes…..while discovering my cure...
https://connect.mayoclinic.org/comment/798505/
syndromes…..while discovering my cure for MCAS
I realllllllly shouldnt post this, because I don’t want to be a downer. But. My immunologist...
https://connect.mayoclinic.org/comment/899233/
And Yes, I had told his MA about the MCAS
Wow! That’s great! 😃 thank you for responding! I too have PVC’s and would LOVE for...
https://connect.mayoclinic.org/comment/1099113/
permeability and gut inflammation improving MCAS
Hi there. I also have anxiety issues, tachycardia & palpitations. I’m extremely sensitive to medications &...
https://connect.mayoclinic.org/comment/864028/
Syndrome, EDS or hyper mobility & MCAS
I’ve been having this issue ever since I had Covid a few years ago. Doctors tell...
https://connect.mayoclinic.org/comment/1182997/
the itching) I suggested it maybe mcas
Hi, I’m really curious… how is everyone getting diagnosed with microclots? Although I have read so...
https://connect.mayoclinic.org/comment/905779/
I was checked for MCAS and supposedly
Finding what helps people with mast cell disorders either with mastocytosis or mcas or the newly...
https://connect.mayoclinic.org/comment/134335/
disorders either with mastocytosis or mcas
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