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Old 05-17-2010, 05:56 PM #1
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dmplaura dmplaura is offline
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Join Date: Jul 2008
Location: Moncton, NB, Canada
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dmplaura dmplaura is offline
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Join Date: Jul 2008
Location: Moncton, NB, Canada
Posts: 2,195
15 yr Member
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Quote:
Originally Posted by barb02 View Post
My neuro did mention the new oral meds that have not been approved by the FDA yet. He also said that I would of course want to try one of them. But a few minutes later he mentioned that I have been stable with out being on a DMD. I think he is a bit unsure of what to advise. I'll cross that road whenever they are approved.

Dejibo -- Are you back on copaxone?
Your news: CONGRATS!!! This is awesome barb

As for your choice to go DMD free.. my neuro advised me to be on a DMD, however I said no way, I know my body, I know my diet's controlling this crappy disease. For me, it was the right choice. For him as the neurologist, it was playing the roulette with my disease, but I think he knows deep down what you said... mild. My GP used the mild word with me. Let's hope we both remain mild-ies !
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2004 to present - Trigeminal Neuralgia
2007 to present - Burning Mouth Syndrome
March 2008 - Multiple Sclerosis DX
05/2008 - Relapse
05/2008 to 02/2009 - Copaxone
10/2011 - Relapse - Optic Neuritis developed
9/2012 - Relapse - Balance issues 1 sided
8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax)
April 7/14 - Raynaud's Syndrome DX
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