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Magnate
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Join Date: Jul 2008
Location: Moncton, NB, Canada
Posts: 2,195
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Magnate
Join Date: Jul 2008
Location: Moncton, NB, Canada
Posts: 2,195
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I am almost always cold, unless I get into a tub of hot water (best thing for me... I know many with MS can't tolerate a hot bath).
Cold to the bone indeed, that's exactly how I am all winter long, and a good portion of the spring/fall. Even in air conditioned buildings sometimes.
I do find that keeping active, I'm less cold than if I just veg. So I walk a lot, and that seems to have helped my personal temperature levels.
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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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