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302 total results
Comments (281)
Any answers? I’m in the middle of this right now at Cleveland Clinic in FL. All...
https://connect.mayoclinic.org/comment/885672/
All the symptoms of MCAS, but 24hr urine ... is, the symptoms of carcinoid and MCAS ... Sounds like MCAS, but nobody in the ... to rule out carcinoid syndrome or MCAS
Discussion: Differentiating Carcinoid syndrome from MCAS?
Support Group: Neuroendocrine Tumors (NETs)
Posted: Jun 26, 2023
The histamine blockers being used for long-haul treatment are over the counter, like Pepcid AC (H2...
https://connect.mayoclinic.org/comment/771331/
haul have symptoms very similar to MCAS ... treatments-for-lowering-histamine-and-reducing-mcas-symptoms ... https://hoffmancentre.com/treatments/mcas
Discussion: Anyone tested for Epstein-Barr virus (EBV)?
Support Group: Post-COVID Recovery & COVID-19
Posted: Nov 9, 2022
I'm so sorry to hear about everything your going through. Currently my daughter is being treated...
https://connect.mayoclinic.org/comment/134376/
Currently my daughter is being treated for MCAS ... be learning and knowing alot about MCAS
Discussion: Mast Cell Activation
Support Group: Blood Cancers & Disorders
Posted: Apr 26, 2019
I have some experience with it. What do you mean by “relatively stable”? It’s my understanding...
https://connect.mayoclinic.org/comment/1141904/
s my understanding that one reason MCAS ... trial and error) and if they suspect MCAS ... I have POTS and HSD/hEDS, and MCAS is ... an allergist with experience with MCAS ... as many people affected by MCAS do
Discussion: tryptase labs
Support Group: Post-COVID Recovery & COVID-19
Posted: Sep 15 10:53am
Have you looked into mast cell activation syndrome? It is becoming more common with Covid long...
https://connect.mayoclinic.org/comment/733786/
eliminate or confirm…written by the top MCAS ... www.ehlers-danlos.com/wp-content/uploads/MCAS-Primer-for-the-Gastroenterologist.pdf
Discussion: Running out of hope
Support Group: Just Want to Talk
Posted: Aug 3, 2022
Glad it was helpful, and I’m glad it sounds like you have a doctor who’s aware...
https://connect.mayoclinic.org/comment/1142213/
s aware of more of the nuance with MCAS ... Since antihistamines are treatment for MCAS
Discussion: tryptase labs
Support Group: Post-COVID Recovery & COVID-19
Posted: Sep 16 12:06am
I'm still not dx'd. I was traumatized by my experience with medical professionals during my first...
https://connect.mayoclinic.org/comment/742116/
books on Histamine Intolerance and MCAS ... I noticed that many of the MCAS medications ... are used for Asthma and many MCAS patients
Discussion: Mast Cell Activation Syndrome: What treatments help you?
Support Group: Blood Cancers & Disorders
Posted: Aug 26, 2022
I have MCAS with co-morbid POTS, IBS, Narcolepsy, and a lot of skin flushing/cold sweating. Symptom...
https://connect.mayoclinic.org/comment/805566/
I have MCAS with co-morbid POTS, IBS ... million good things about VNS for pots/mcas ... Like most people with MCAS I'm at
Discussion: Vagus Nerve and TENS unit
Support Group: Brain & Nervous System
Posted: Feb 2, 2023
Hi. I can relate to your frustration of not having a diagnosis. It took 6 years...
https://connect.mayoclinic.org/comment/239830/
latest: mast cell activation syndrome (MCAS ... I have done a lot of research on MCAS ... main tests that is used to diagnose MCAS ... manage them. there is no cure for MCAS
Discussion: Difficult case, several diagnosis, no solution yet
Support Group: Autoimmune Diseases
Posted: Feb 5, 2019