EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at
Experience Project.
Actually, the brochure in the link only mentions a presentation on CVI - Chronic Venous Insufficiency in the "limbs," and says nothing about the Cerebrospinal version. Wonder if CCSVI actually came up?
Quote:
10:05 am SCIENTIFIC SESSION VII
Chronic Venous Insufficiency
Moderators: William A. Marston, MD &
Nicos Labropoulos, MD
Educational Objectives: After completion of this
session the participant will be able to (1)
identify and treat atypical causes of limb
swelling, (2) understand the effect of stretch on
TGF-b expression by dermal fibroblasts, (3)
determine changes in the vein wall induced by
venous thrombosis and (4) understand the key
components of measurement of quality of life
in venous disease.
_________________ Dx with MS & HNPP (a hereditary peripheral neuropathy) July '03, but had probably had MS 30 yrs. I've never taken any prescription meds for MS or MS symptoms (except 1 year experiment on LDN, but I don't consider it an MS med anyway ).
12th february is the day
do we happen to know a date for the results of this debate?
Quote:
Endovascular Treatment For Chronic Cerebrospinal Venous Insufficiency In Multiple Sclerosis: A Longitudinal MRI Blinded Pilot Study
P. Zamboni1, R. Galeotti1, B. Weinstock- Guttman2, G. Cutter3, E. Menegatti1, A. M. Malagoni1, I. Bartolomei4, J. L. Cox2, F. Salvi4, R. Zivadinov2 - 1University of Ferrara, Ferrara, Italy; 2NY State University in Buffalo, Buffalo, NY; 3University of Alabama, Birmingham, AL; 4Bellaria Neurosciences, Bologna, Italy
Hi Squiffy,they did talk about CCSVI and they had a workshop about it;
look at my posting under
22nd Annual Meeting of American Venous Forum in Amelia Is,FL
Hi Squiffy,they did talk about CCSVI and they had a workshop about it;
look at my posting under
22nd Annual Meeting of American Venous Forum in Amelia Is,FL
Thanks, guys. I THOUGHT I had already read about it on the forum, but couldn't find your thread again, Nunzio. CCSVI was presented at 8:30 am on the 12th.
So...I suggest going to the other thread instead of this one :
http://www.thisisms.com/ftopict-10188.html _________________ Dx with MS & HNPP (a hereditary peripheral neuropathy) July '03, but had probably had MS 30 yrs. I've never taken any prescription meds for MS or MS symptoms (except 1 year experiment on LDN, but I don't consider it an MS med anyway ).
Sorry Nunzio, missed that thread and someone sent me the details this morning so thoght I would share it here. _________________ The Multiple Sclerosis Resource Centre
You cannot post new topics in this forum You cannot reply to topics in this forum You cannot edit your posts in this forum You cannot delete your posts in this forum You cannot vote in polls in this forum
We encourage you to also visit our Multiple Sclerosis support community on Experience Project.
Experience Project is a vast and powerful community where people connect anonymously through life experiences. It's made by the same people who built This is MS,
on the premise that no single life experience-- like having MS-- defines a person. EP now covers over 5 million true stories about every possible life experience. Find and share yours!
Forum FAQ
Search
Usergroups
Profile
Log in
).
