Ourfullhouse, crazy with the st louis thing. i just started seeing specialist there. “i live about 2 hours away” my daughter and i got diagnosed with EDS type3 in december. in st louis aswell. i have yet to make up my mind about the doctors there. Though they did make an attempt when they was wrong (saying pots and EDS was not connected) to run me down in the hallway to tell me i was right. so they are atleast trying. 🙂 As far as the MS thing. In my Gut i have this feeling this is what it is. But you would think with 5 mri of my brain in the past 18 months they would atleast see lesions right?