This Is MS Multiple Sclerosis Knowledge & Support Community

I did a search, but got no info regarding how to contact Dr. Simka. Does anyone out there have this information?

I found a website that had an e-mail address, but it kept bouncing back to me.

Any help would be appreciated

Hi Ana, thanks for your comments and welcome! My insurance paid for this procedure, so no class action for me, but it sounds like a good idea if for nothing else, to wake em up that we refuse to hear anything but progress in this area. Not sure if I would sue any particular doctor per se. Last thin...

zap wrote:Same day as me @ Stanford! Good luck!

Are you scheduled to have the whole procedure? If so, how did you get scheduled? What did you do to get in touch with Stanford?

Looking forward to your reply.

To All of You:

Thx for the support and the info. I am seeing my gp on Wed. Will see if I can get a scrip then. Again Thx.

Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
dual stents placed 5/09

Cheerleader:

Where and who treated your husband? How did you go about the process of obtaining the procedure?

[quote="jenf"]Hi Michelle, Dr Herbert was the 3rd Neuro I went to after my introduction to this wonderful disease this past spring. I used the word "was" because I went to him once for a consult, asked him about LDN, and he chuckled and advised me with that gentle "pat on th...

I just emailed Dr. Grossman at NYU to see what they are doing about screening for CCSVI as they have a tesla 7 machine and I found out while doing research on the NYU site that he collaborated with Dr. Haacke on his research so he should be very familiar with it. As soon as I hear back I will post....