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#1 | ||
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I was thrilled when I realized that Magnesium helped....but I didn't realize that doctors consider it drug to be dependent on. I don't think my doc knows I even take it!!
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Dx: RRMS Jan 2010; LDN: March 2010-Dec 2010; Aug 2012-Nov 2012 Tysabri: Feb 2011-March 2011 reaction Gilenya: August 2011 reaction Copaxone: October 2011 reaction Tecfidera: May 2013 reaction |
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"Thanks for this!" says: | dmplaura (08-19-2011), Motors Mommy (09-11-2011) |
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#2 | |||
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Magnate
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If your GPs are like ours.... they'll fluff off discussions about a lot of vitamins/supplements/alternative treatments. Sometimes founded, most times not. The only my GP actually backs me on is Vitamin D, but she knows I'll take what I find works for me, so she leaves me be.
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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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"Thanks for this!" says: | Motors Mommy (09-11-2011) |
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