OK guys!!! so I got diagnosed in November!!! prior to that I was having symptoms for about three years! I was waiting about six months for an MRI. Finally got it when I got admitted in November for blurry vision! since then, I’ve had two big flareups which had me back in the hospital and the only thing they did was jacked me up on steroids and then sent me home with nothing.. no steroids, no pain medicine… nothing! Only thing I been taking is Pregabalin! It helps with the aches in my hands, but that’s about it! I’m not really a pill person, I try to stay away from them but I wake up some mornings and my whole body hurts and I can barely walk. I live in a small town in the closest Neurologist is about two hours away… I finally have an appointment on February 2!! what are some things I should ask? What should be my first step in this long journey?!