This Is MS Multiple Sclerosis Knowledge & Support Community

I was at my neuro's a week ago and he talked about something very similar being common. I don't recall what he called it, but it sounds like something to talk to your dr about.

Yes Axiom, Dr Volmer was the person I saw the first time I went to Barrows. After that initial visit, I met with the nurse practitioner each visit.

I was originally seeing a Dr (whose name escapes me) at Barrows, but after the first visit, I always met with his PA. He left to move to Colorado, and Dr Campanella (sp?) took over for him. She did a good job, but she is moving to the VA hospital. It seems like Barrows is a stepping stone to another...

Hi Everyone, I haven't posted too much here, I have just been lurking. I have been a patient at Barrows since 2003 (dx in 2002). They are now in the process of bringing in another new Neurologist to run the MS Clinic there. Getting introduced to another (this will by my 4th there, 5th overall) Neuro...

Hi Zipfed and CRHinv,

I am Grant and I live in North Phoenix. I am extremely interested in trying to get in to see Dr Dake.

Can you give me some information about how you approached your Dr and how you got into Stanford?

I hope you don't mind if I PM you both.

Thanks,

Grant

Hi guys, How did you go about beginning the process of finding out if this is something that is affecting you? I was diagnosed with RRMS in 2001 (it started in 98). I have copies of my MRIs on CD, but I can't tell where my veins are... I am not a dr :) I am intrigued by this, and like everyone here,...