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Brit recently moved to minneapolis! Any oms'ers please holler!!!
I'm in the Minneapolis area, what Neuro do you see?
Rebecca Hoover is from Minnesota, not sure which part. You can contact her via Facebook: https://www.facebook.com/rebecca.hoover.33


OMG December 2011 OMS January 2012 OMS Retreat March 2012 Benign MS Sep 2015
Two Very Mild Relapses since diagnosis. Copaxone May 2013 No new lesions on MRI since diagnosis
Yep, Rebecca is in Minneapolis-St Paul, there is a recent blog by her here:
http://www.overcomingmultiplesclerosis. ... al/?p=1101
Rebecca's story is featured in the book Recovering from Multiple Sclerosis real stories of hope and inspiration
She would love to hear from you!
I'm in Texas! :) Holler anytime! Rebecca would be a great blessing if near ya!
I'm in Atlanta, but if there is ever a USA OMSer meet up, I will fly anywhere and be there for it. Even if it's just a nice vegan lunch somewhere. This site is the only contact I've ever had with like-minded MS folks.

In fact, I've only spoke to one person with MS since diagnosis and it was such a downer, I've been avoiding it.

I travel quite a bit for work. Next time I'm in Minneapolis I'll post here. I can guarantee it will be after it warms up a bit though!

I'm just a few hour drive down I-35 in Kansas City. Welcome.

I'm in North Carolina!
Wow! Look at all these Minnesotans and surrounding states! I am too (Mn) and so happy it was finally warm enough to enjoy walking outside today! I had been going to Mpls Clinic of Neuro, but they are quite traditional and too pushing of meds for me. Open to ideas on who to see if you have a good one, but I am not too worried about checking in with one. Minnesota has many awesome alternative health practitioners for whom I am very thankful.

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