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302 total results

Comment

I am using the Leading Edge Clinic established by Dr. Pierre Kory. The telehealth visit are...

https://connect.mayoclinic.org/comment/1073707/

I have MECFS, MCAS, PAH, Type 1(previous

Discussion: Anyone have any success with going to an LC clinic?

Support Group: Post-COVID Recovery & COVID-19

Posted: May 24 8:58am

Comment

Hi @rhawk314, I'd like to add my welcome and some info to add to the great...

https://connect.mayoclinic.org/comment/729893/

Robert, you ask about Mayo Clinic and MCAS

Discussion: Mast Cell Activation Syndrome: What treatments help you?

Support Group: Blood Cancers & Disorders

Posted: Jul 23, 2022

Comment

You have almost the exact same symptoms/chronic illnesses that I have. I have found a clinic...

https://connect.mayoclinic.org/comment/1074973/

now have Dysautonomia, POTS, MECFS, MCAS

Discussion: Long Hauler Worsening Symptoms and Doctors are Stumped

Support Group: Post-COVID Recovery & COVID-19

Posted: May 26 10:10am

Comment

Has anyone developed nystagmus or other eye movement problems from their hEDS (not sure if it...

https://connect.mayoclinic.org/comment/1171519/

was finally diagnosed with hEDS and MCAS

Newsfeed Post: Head and Neck Concerns in EDS/HSD

Blog: Ehlers-Danlos Syndrome

Posted: Nov 11 5:37am

Comment

yes, I went to see him on tuesday. I feel like he has started becoming more...

https://connect.mayoclinic.org/comment/134371/

which would also allow him to look for MCAS

Discussion: Mast Cell Activation

Support Group: Blood Cancers & Disorders

Posted: Mar 16, 2019