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335 total results

Comments (309)

Hello, I almost never am logged in here anymore (in fact i had to reset my...

https://connect.mayoclinic.org/comment/330159/

and what turned out to be Primary MCAS

Discussion: Ehlers Danlos Syndrome (EDS) & HSD, calling all types!

Support Group: Bones, Joints & Muscles

Posted: Dec 20, 2020

Gosh, I sure hope you do. Good to hear that other symptomes hve gone. There is...

https://connect.mayoclinic.org/comment/801450/

Pycnogenol COVID-19 pilot study – MCAS

Discussion: How long have you had post-covid?

Support Group: Post-COVID Recovery & COVID-19

Posted: Jan 25, 2023

From the USA…….I am so sorry that this is your life right now……I do know how...

https://connect.mayoclinic.org/comment/826099/

same is true of the millions who have MCAS

Discussion: How do you deal with oral allergy syndrome and histamine intolerance?

Support Group: Autoimmune Diseases

Posted: Mar 14, 2023

Doctors really need to stop saying things like “Sick people itch” my goodness. I had my...

https://connect.mayoclinic.org/comment/309046/

out to be all explained by Primary MCAS

Discussion: What do you do for Neuropathy itch?

Support Group: Skin Health

Posted: Dec 20, 2020

Iḿ so impressed by your persistence across the specialists, because seeing all of these will be...

https://connect.mayoclinic.org/comment/1099430/

for mast-cell activation syndrome (MCAS

Discussion: Phlegm in my throat and post nasal drip after Covid

Support Group: Post-COVID Recovery & COVID-19

Posted: Jul 4, 2024

Update on progress: Antibiotics for gut might be a cure!?!… Valacyclovir didn’t have much effect. Unfortunately....

https://connect.mayoclinic.org/comment/1102175/

I was found to have MCAS and hEDS.

Discussion: Are Antivirals and/or Antibiotic cocktails the Cure for LC?

Support Group: Post-COVID Recovery & COVID-19

Posted: Jul 9, 2024

Hello @smbryce1, thank you for your responses. Yes, let's connect, whether professionally or as a friend....

https://connect.mayoclinic.org/comment/330162/

I think it may be MCAS but I have still

Discussion: Ehlers Danlos Syndrome (EDS) & HSD, calling all types!

Support Group: Bones, Joints & Muscles

Posted: Dec 21, 2020

Hello, bluecow! I started out with Code Age Beef Kidney. Finished the bottle and switched to...

https://connect.mayoclinic.org/comment/774053/

." I have heard of many MCAS sufferers

Discussion: What testing should I look forward to be properly tested for MCAS

Support Group: Autoimmune Diseases

Posted: Nov 16, 2022

Hi @gabrielm I have never posted on one of these forums before but your original post...

https://connect.mayoclinic.org/comment/203153/

And learning about MCAS.

Discussion: Mysterious shortness of breath: What has helped you?

Support Group: Lung Health

Posted: Sep 5, 2020