The neuro I went to for four years moved across the state. I loved him, and I trusted him. He listed to me, I listened to him. It was great.

I've only seen my new neuro once. He seems okay. I'm his only patient on TY, but his office got everything set up for me to change infusion centers to one that DH used for his chemo, great nurses, and just five minutes from the house.

I just have to get used to this new one and quit comparing him to the last one.

I'm at the point in my MS where I make more decisions in my treatment, whether or not to try something for MS. I try to stay informed, but there's so much going on now with treatments. I'm not afraid to question my neuro (or PCP) about things, where I used to be like a sheep and do whatever my doctor recommended. It was very liberating to take charge of my own health!