I do have MassHealth this year, so that's good.
Tomorrow I start Florinef, a blood volume steroid.
I went to a neurologist in December after my 2nd concussion, and he cleared me for light exercise/PT. He seemed to think POTS was bigger than my concussions. I have a referral for an autonomic specialist in Boston, should I need it, but they mostly just do tests (and some are really scary/uncomfortable, with not much feedback...tilt table, sweat room). There's not much they do for POTS besides florinef/midodrine and lifestyle adjustments.