The most impressive moment, when you can give a patient the idea what is happening to him, that his impressions and feelings of the own body are real and not of psychosomatic origin. Seeing over a hundred patients a day… by statistics there must be at least 17 amongst them affected by MCAS. Even more when working in a field that is a key area for MCAS patients.. thanks for the video 👍🏼🙌
Dr. S, I have MCAS and HAT, no EDS or POTS, but a progressive peripheral neuropathy and inflammatory arthritis. Would appreciate any insights you have on this constellation of disorders. Thanks!
Interesting. Just started to rely on Advil heavily as I traveled last week and walked so much and all my joints hurt. My MCAS must manifest in prostaglandin release not histamine release! Cuz my joints are on fire!
Seems like a waste of time to chase numbers. Maybe easier/cheaper to see if the stabilizing meds like Singulair or ketotifen (or both like I'm on!) help.
The most impressive moment, when you can give a patient the idea what is happening to him, that his impressions and feelings of the own body are real and not of psychosomatic origin. Seeing over a hundred patients a day… by statistics there must be at least 17 amongst them affected by MCAS. Even more when working in a field that is a key area for MCAS patients.. thanks for the video 👍🏼🙌
You're welcome and thanks for your efforts towards helping patients identify these issues.
Dr. S, I have MCAS and HAT, no EDS or POTS, but a progressive peripheral neuropathy and inflammatory arthritis. Would appreciate any insights you have on this constellation of disorders. Thanks!
Interesting. Just started to rely on Advil heavily as I traveled last week and walked so much and all my joints hurt. My MCAS must manifest in prostaglandin release not histamine release! Cuz my joints are on fire!
Seems like a waste of time to chase numbers. Maybe easier/cheaper to see if the stabilizing meds like Singulair or ketotifen (or both like I'm on!) help.