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Hi everyone,
I have mitochondrial dysnfunction as well mcas, cci, ijv compression, Lyme and severe dysautonomia. Urolithin A was recommended to me for mitochondrial issues, and I saw a paper saying it also boosts collagen production and a posts here or there saying it seemed to help floxed patients (I did take levaquin shortly before a great worsening of my issues).
But I also read it boosts memory T cells, which has me wondering if it'll make my mcas issues worse. I'm down to 2 foods I can eat every day. There are a couple others I can eat that break my biofilm so I can only eat them on days with antibiotics. So I guess my question is has anyone/how many of you with mcas issues have taken Urolithin A, and did it affect your mcas issues for better or worse? Also have any of you found it to help with dysautonomia, cci, energy, or infections.
Thanks!
I have mitochondrial dysnfunction as well mcas, cci, ijv compression, Lyme and severe dysautonomia. Urolithin A was recommended to me for mitochondrial issues, and I saw a paper saying it also boosts collagen production and a posts here or there saying it seemed to help floxed patients (I did take levaquin shortly before a great worsening of my issues).
But I also read it boosts memory T cells, which has me wondering if it'll make my mcas issues worse. I'm down to 2 foods I can eat every day. There are a couple others I can eat that break my biofilm so I can only eat them on days with antibiotics. So I guess my question is has anyone/how many of you with mcas issues have taken Urolithin A, and did it affect your mcas issues for better or worse? Also have any of you found it to help with dysautonomia, cci, energy, or infections.
Thanks!