This Is MS Multiple Sclerosis Knowledge & Support Community

13%? why the pie chart states 25%...

Blaze, I'm feeling that way too. Unfortunately I don't think that it will be possible before a couple of years here in Canada. I anticipate that all (100%) studies done by the MSS (Canada) and MSS(US) will be negative. I'm too pissed off to be positive here.

I'm proud to offer you.... Dr. Randall Schapiro'S comments. Yes, he is a member of US MS. [/url] http://ccsviclinic.ca/?p=622 [/url] A respected MS neurologist, researcher and educator has slammed the controversial CCSVI hypothesis, also known as the “Zamboni Liberation Therapy”. Dr. Randall Schapir...

I just came across a document saying at page 35 that coffee modifies blood floow in the brain, Should I stop drinking coffe :

http://www.ms-mri.com/presentations/goo ... script.pdf

Happy new year!

Is Sandy really being prevented to do his study or it's just a lack of funding. I don't think he has applied to an IRB in Canada right?

Dr. Zamboni mentioned the Putnam dog study recently. He noted that at 3 months no MS in the dogs, 6 months no MS, but at 9 months ALL THE DOGS developed MS (at 19:20 in the presentation). Commentary: Does chronic venous insufficiency play a role in ms pathogenesis? < shortened url > Putnam publishe...

Actually, he said, ''if you keep no narrowings, you have no more relapses'' You can twist it the way you want but this is what he said...

Come on concerned... It comes from Zamboni himself during his interview at CTV. ''If you keep no narrowing you have no more relapses'' But in fact relapses are not always related to progression. Lots of people here state that it stops the progression. But in fact nobody knows yet... Use the force!

he is edss 0 6 years after dx or so. Another disease? Whatever...just saying what i saw. The fact is that MY veins are a mess (with collateral circulation) even after the operation comparing to his. So, i guess opening them was a good thing. Same as me, EDSS:0 after 6 years, but I have a reflux in ...

Hold on guys! I had my first episode 6 years ago, numbness (active lesion) and then 2 weeks after, gone. Now I can fell some numbness at the same place. Come on... Tell me that it could'nt only be Lyme desease.

Is it per balooning and per stent? I mean 2000$ times number of ballooning? What about follow up?

30 people is a good start but I HOPE that the results will be published before 2011.

Here is a letter from the College des medecins du Québec. It's in french.

http://www.cmq.org/medias/profil/commun ... nique.aspx

Cool. Bizarre pour une fille qui n'avait pas été diagnostiquée positive CCSVI à Westmount square.

Honestly, all these debates are good but they'll all lead to nothing for the next, let's say 6 months. If I have one relapse, I'm gone to NY.