As some of you already know, I just got home from 3 days in Columbus doing tests, blood work, & much more. The trip was so worthwhile & I even got to do a few not-illness-related fun things while I was there!
The first doctor I saw was an endocrinologist. He did so much blood work on me I thought I was gonna need a transfusion afterward! In total, he took 22 vials of blood (some were the big vials) & I was poked 10 times. -2 veins were blown out in the making of this blood work.- However, I will hopefully get a LOT of answers because he suspects hyperadrenergic POTS. He was so nice & he even called us into his office to have a chat about my treatment. He is working closely with my cardiologist (main treating doc) to come up with a plan that will help me the most.
After the endocrinologist, I went straight to a new neurologist. He was so knowledgeable on POTS & the co-conditions that are seen in many POTS patients. He immediately said that I have a movement disorder (not sure exactly what yet), and he strongly suspects EDS type 3 - hypermobility. I've been told I have this, but I was not evaluated properly. Finally, he suspects Chiari Malformation type 1 and ordered an MRI. I've also been told I have this but the doctor wasn't knowledgeable at all so I want to be sure. He was so pleasant and seemed genuinely interested in my case and concerned about treating me. He is also working with my cardiologist and developing a plan, which will hopefully include medication to treat my hemiplegic migraine and NDPH.
I had a tilt table test also, which was not as bad as I expected & it was so very informative. My blood pressure dropped to 50/20, and my cardiologist could not believe I was conscious. He did not want to see me faint since this (& my heart rate of 128) classified as a definite positive for POTS. Everyone at the Midtown Medical Center was so nice and caring. They brought me warm blankets, cheered me on during the test, and walked me to the car. A special shoutout goes to Stacy, the lovely nurse who helped me through everything and was so sweet! Oh and to the guy who couldn't get a vein until 3 minutes of digging, it's not you its my veins! Haha. Anyway, every single person I met at the hospital was so pleasant, even though there was a slight issue with scheduling. I was so pleased with everything.
My cardiologist scheduled me right after the tilt table test, so that he could discuss everything with me and my grandmother. He takes us back to his office, and the first thing he says was "if only that jerk would have done the test like I'd asked him to, it would've confirmed everything he was questioning. When I ask for a pizza, you don't need to tell me what I want on it, you just need to give me the pizza!" I love him so much😊. He explained how the test went, & how I definitely have POTS. Then, he asked me to try a gluten-free diet for 2 weeks, because he suspects Celiac disease. He then said that he was going to talk with the endocrinologist and neurologist over the next couple of days, then he would call us with everything they want to do. They want to organize a treatment plan that will address as many of my medical issues as possible without any inpatient stays or extensive testing. He actually cares about me & listens to me!❤️
I was beyond happy with everything that went on this week, and I finally feel like I am on the right road to feeling better in the future! I know my illnesses are "chronic", so I won't be cured, but that doesn't mean I can't have some relief, right? I hope everyone else is having an okay time, and if you have any questions, you can click that snazzy "add comment" button and ask your heart out!
FIGHT LIKE A SPOONIE!
xoxo,
Johna
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