I am still not improving with my POTS condition & the specialist I have been seeing since 2021 has only had video appts with me & even now refuses to have in person appts. I have struggled with the medication side effects because it causes extreme fatigue for me & his biggest problem is he just didn't believe me, & basically said as much, "oh I don't think its that" he said. π. I knew for sure it was cause nothing else had changed but I gave it a chance for about 2 yrs, & I finally said no more, I messaged him & said its not doing what its supposed to cause I'm still having the symptoms & on top of it I'm in bed most of the time so there is no quality of life, it makes no sense, he finally agreed I should stop it, I told him the same thing a few months ago & he wanted to raise the dose, I told him absolutely Not!.
So I'm off that med & my primary doctor has been trying to get me another specialist but it's difficult - took 2 yrs to get the initial one. We're trying for Stanford medical center now, since they don't want to approve Mayo Clinic in Arizona, π‘ hopefully this goes somewhere, they do have a Neurology dept that treats POTS patients so thats hopeful at least. I'm so exhausted with the nonsense, and now with the added mess up from my dentist, damnπ€·♀️ what's next? I'm just hoping its not permanent whatever he did to my nerve, but that's for a lawyer to figure out if it comes to that.
I'm really too short tempered for all this bad luck lol, it's not good for my hot head, foul mouth & bad attitude ππ why can't life be simple right? You know after menopause, women just tell it like it is with No filter & I did that before, so just imagine it X100 ππ well hopefully I get the new referral & the MRI proves what the dentist did to me cause its not cool & somebody needs to be held accountable & maybe life can start to get back to normal one day, haha, yeah normal, whats that? π€ͺπ.

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