Darlene Posted December 6, 2011 Report Share Posted December 6, 2011 i was dx with POTS in 2005. i see dr. blair grubb in toledo. i did ask him about mast cell. all he said is that it was hard to dx. i really do believe i have this. my cousin (who happens to be a dr.) was just dx recently with dysautonomia too. when he told me his symptoms i told him it sounded like mast cell. he seen dr. afrin, and sure enough he does. well, i don't have money to drive to north carolina or where ever. i wish i knew somewhere i could go locally. cleveland clinic maybe? Quote Link to comment Share on other sites More sharing options...
lieze Posted December 6, 2011 Report Share Posted December 6, 2011 What treatment regimen is your cousin following?Could you try something similar and see if your symptoms subside?I think I most likely have it or chemical sensitivity.I'm not sure there is a difference.I think it could be a problem with immunity also.First and foremost if it's possible avoid your triggers. Quote Link to comment Share on other sites More sharing options...
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