Mast cell activation

[sq1111]

Hi everyone. I'm sharing the first part of my interview with Dr. Tina Peers on her approach to treating mast cell activation syndrome, a common comorbidity of EDS.

It took me a long time to find a doctor who knows the condition and was willing to be interviewed. I hope you find it helpful. Future interviews will discuss symptoms (in detail), how to get a diagnosis, root causes, the relationship with histamine & hormones.

This video is for informational purposes only and is not meant to medically diagnose anyone in the group.

thecommunality.com/hit-mcas...

youtu.be/em-BxpImE6A(Not working as expected?)

[Mabsy]

Thank you so much for that video.

Mabsy

[sq1111 in reply to Mabsy]

Hi Mabsy, I hope it was helpful! Follow the channel for more updates. There will be 3 more videos in the interview series.

[Mabsy in reply to sq1111]

Definitely informative for me and I look forward the follow- ons. 👍

[MrsMouseSJ]

Thank you so much for posting this - really helpful indeed. I don't have EDS but autoimmune issues and a different genetic condition. However I have long suspected that I have some form of histamine or MCAS running alongside.

[Birch_]

This is really interesting. Is there a transcript available? There are quite a lot of drug names and supplements mentioned which I would like to look up but I didn’t quite catch them.

[TurquoiseTime]

Hello sq1111,

Thanks so much for putting this together and your work involved and eagerness to share with others. What was the name of the medication that helps with the gut/IBS symptoms? I didn’t catch what she was saying.

Thanks so much!