Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
MsBabs
After my dx 7 years ago, it seemed like I had several MRIs. When I switched to my current neuro 5yrs ago, I thought it was unusual that he never ordered an MRI for me. He said "I treat the patient not the MRI" and I thought that was fabulous at the time. I started Tecfidera last year and expected I would need an MRI at that point to get a baseline reading, but no. Now that I've been on it a year I'm curious to know what's going on in my head, but he still isn't ordering one.
Does anyone else have a neuro with this philosophy? I should add that my doc is very well known in the MS field, and I currently have very mild MS, and there's no reason to think anything is wrong. I'm just curious. Thanks!
Does anyone else have a neuro with this philosophy? I should add that my doc is very well known in the MS field, and I currently have very mild MS, and there's no reason to think anything is wrong. I'm just curious. Thanks!
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I'm still on the fence about what I want to do. It's been nearly 6 years since I've had an MRI but I haven't had any sort of relapse in that time... just a lot of annoying symptoms. I don't mind the MRI process (I find it kind of fascinating and psyche myself up by pretending it's an exotic spa treatment! :) ). I guess I would just like to know something oNone way or the other about how my brain looks now. Not that it would change My treatment approach, but just for my own understanding. My next appt is in a few weeks and I will definitely talk to the neuro more about it.
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