Ehlers-Danlos Syndrome and Peptides

I have diagnosed hEDS and POTS, and am getting testing done at the end of the week that we expect to confirm MCAS and some form of gluten sensitivity so this thread is very interesting to me. I am going to add MOTS-C to my routine soon and see how it works for me!

I have never taken reta, but I have been on tirz now for about 4.5 months and it has been a godsend for me for pain and inflammation. I noticed a difference in both the very next day, and a coworker told me my face was visibly less puffy 36 hours after my first pin. Even if I hadn't lost any weight to this point, the amount of relief it's given me would make every pin worth it. I see a specialist who focuses on EDS treatment, and she told me that her patients that also take tirz, whether it be prescription or otherwise, see the same benefits for pain and inflammation levels.
I have struggled a lot with MCAS for years, after a severe mold exposure. Of the many things that can help, nasal probiotics ended up being very effective.
That's awesome that you saw the reduced inflammation with tirz!
 

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