hiya,
only just been diagnosed with PoTS so not even looked into mast cells yet but its been something i’ve been thinking about for a while…. will give my dr a little while to mull over all the PoTS info i gave him before tackling mast cells with him. and give me time to develop a good argument for testing! PoTS was an epic battle to get diagnosed and has taken several years (although much less than getting my EDS diagnosis 😆
will be looking at your video again now i’ve had confirmation that my PoTS symptoms are real and not in my imagination as my old doctor told me. i changed doctors after that, she told it to me for long enough (about the eds diagnosis) and i was fair and gave her a 2nd chance but she blew it! 😆
fi