This Is MS Multiple Sclerosis Community: Knowledge & Support

Has anyone in or near Madison, WI contacted any IRs locally? I know UW Madison is doing a study of CCSVI funded by the NMSS but was wondering if there was anything else going on?

You can pm me with info to keep it private...

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Dxd 1994 RRMS, 2008 SPMS
Climb on!

35 people viewed my original post. Any of you want to work with me to make some calls and educate some dr.s in the Madison, WI area? PM me.

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Dxd 1994 RRMS, 2008 SPMS
Climb on!

I'm in MN, so always interested in goings-on in the general upper Midwest. I am not aware of any docs in Wisconsin currently testing or treating but hope you can get one started. Do you have all the information you need for contacting them? There's a website with all possible IRs for every state. And the research sticky here is useful if you want to include Dr. Zamboni's endovascular treatment research or something else. Best wishes. Every doc we have was found by someone doing the legwork.

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"However, the truth in science ultimately emerges, although sometimes it takes a very long time," Arthur Silverstein, Autoimmunity: A History of the Early Struggle for Recognition

sent you a PM did you get it?

Nope. And, I've been calling local IRs' - no positive response so far....

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Dxd 1994 RRMS, 2008 SPMS
Climb on!

I live about 2 hrs from Madison, i have not been able to find anyone interested either. If you find someone let me know, i'll do the same

I am in UP of MI and sent info to IRs in Green Bay, Marshfield and Marinette with no bites... But good luck with your quest - it will happen! I did not do good follow-up but (excuses, excuses).