View Single Post
Old 01-26-2010, 08:49 AM
dmplaura's Avatar
dmplaura dmplaura is offline
Magnate
 
Join Date: Jul 2008
Location: Moncton, NB, Canada
Posts: 2,195
15 yr Member
dmplaura dmplaura is offline
Magnate
dmplaura's Avatar
 
Join Date: Jul 2008
Location: Moncton, NB, Canada
Posts: 2,195
15 yr Member
Default

I read that article and honestly it sounded like media person playing devil's advocate to pull a story out of their rear end to fill a paper for the week.
I will agree that this isn't an outright 'cure', and it could come with complications and such that we don't truly know the scope of at this time, but what's important to PwMS is hope and new theories, instead of reading the same regurgitated stories we've seen over and over again.
I'm biased in my opinion largely because I'm a PwMS who can see the relationship between blood flow and the body's reaction as such makes entirely too much sense.
__________________
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
dmplaura is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Jules A (01-26-2010), Kitty (01-26-2010), Natalie8 (01-26-2010)