This Is MS Multiple Sclerosis Knowledge & Support Community

My wife's PCP told her that hemochromatosis was not an issue for her because of her "monthly" blood loss. Now, many years after her dad and brother's hemochromatosis, here we are wondering. We certainly plan to follow up on the scans. Hopefully, our PCP won't have an issue ordering them. S...

No specific family history of MS. However, my wife's mother developed Gillian Barre syndrome five years ago. The GB left my wife's mother with severe neuro deficts and wheelchair bound. On another note in association with CCSVI, my wife's dad and brother have both been diagnosised with hemochromatos...

The information on CCSVI is what originally brought me to this site. Our local neuro is open to the research but skeptical at this point. We plan to pursue getting the scans and images of my wife's veins next month either through neuro or our PCP. The neuro we saw at Johns Hopkins completely dismiss...

Hi everyone. My name is Lewis and I live in Greenville, NC, USA. I have been following this site since November 2009. I decided to join and make an introduction since my wife received her official MS diagnosis on March 23, 2010. Our Story: On November 1, 2009 my wife began having minor numbness and ...