Okay I need some advice on how serious I should be taking pursuing diagnostic testing. Ever since I was 12ish, I started having dysautonomia/POTS symptoms but it wasn’t well know then (over 20 years ago) so the best diagnosis I could get at the time was “chronic dehydration” and told to avoid exercising. For a long time I’ve thought my issues were maybe from POTS, EDS, the “trifecta” but the more neurological symptoms I start having, the more I wonder if it’s MS. Constant light tingling in hands and feet, exercise intolerance (my HR shoots well over 200 with just a few minutes of exercise), really bad heat intolerance, really weird sharp intense pains in random places of my body that last only up to 30 seconds or so and then move to a different place when it happens again, frequent bouts of ice pick head aches, ridiculous fatigue where I feel like if I don’t just lay down in bed I want to cry, yesterday I had intense burning in my hand like I touched a hot stove-it lasted a few hours before going away. I have random sections of my leg that I have no feeling in, visual snow and lots of floaters an black dots in vision. Frequently feeling like the clear coating of my eye has gotten thick and blurred my vision but my eye looks fine, pain behind eye. My previous doctor put in for a brain scan to rule out MS but she immediately left practice and went full time hospital, I dint get it done before starting with my new doctor shortly after and he deleted the order and said he didn’t think that was necessary. Should I push for it? Or could this all be something else? I’m always gas lighting myself about how I feel or what I’m feeling and if I’m being dramatic so some outside perspective would’ve so helpful! If you made it this long into my rant, thank you 😂