Dr. Kelly McCann, MD on MCAS, POTS, and Mold Toxicity

[@lindapelle8738]

Great information coming from an Interstitial cystitis sufferer I appreciate this interview immensely. Thank you 🙏 I’d like to see another video where you let her go down some rabbit holes a little further.

[@christinam777]

This video gives me hope

[@quitemountainwoman1592]

Thank you 🙏

[@christinam777]

Im going to try zyrtec. I know for a fact its mycotoxin for me with sonw udnerlyong predisposition from those childhood marker. Now ive bwcome MCS and cant stop the swelling and neuropathy. When the exposure happened, before i fiund the boarload of mold i almost died from this and was diagnnoaed wirh pots and dysautonomia. Then i found iut why!

[@kelliechantler1402]

I’m wondering about root cause. I hear so often that most of the time mcas results from mold or Lyme. But then also that those with the Pentad eg eds or hypermobile folks it goes hand in hand with them. Is it the case then that those with the hypermobility also will have had to have a mold or Lyme issue or is there mcas just due to their connective tissue issues.

[@glenhunt1287]

ρгό𝔪σŞｍ