This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
It is currently Wed Jun 19, 2013 3:36 am


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 23 posts ]  Go to page Previous  1, 2
Author Message
 Post subject:
PostPosted: Mon Nov 30, 2009 9:07 am 
Offline
Family Elder
User avatar

Joined: Mon Sep 10, 2007 3:00 pm
Posts: 4695
Location: southern California
sorry, guys. I've been getting letters/e-mails in Italian from folks, and haven't had time to translate and figure out what's been going on over there. I'll try to look into it today, do some translating and figure out how we can help them.

My Italian is food and opera...not really helpful in this situation, but we'll figure it out....
cheer

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


Top
 Profile  
 
 Post subject:
PostPosted: Mon Nov 30, 2009 9:21 am 
Offline
Family Member
User avatar

Joined: Mon Aug 17, 2009 3:00 pm
Posts: 51
tzootsi wrote:
Here's the same woman speaking in English:

http://www.youtube.com/watch?v=Bnx5m6hispY


Yeah thanks, pretty Itlalian though even if she speaks English, isn't it? :P

At 6:45 she starts adressing the point and that doesn't sound very dramatic. Nice talk, anyway :D


Top
 Profile  
 
 Post subject:
PostPosted: Mon Nov 30, 2009 9:31 am 
Offline
Family Elder
User avatar

Joined: Tue Aug 04, 2009 3:00 pm
Posts: 445
Location: colorado
Boreas wrote:
tzootsi wrote:
doesn't sound very dramatic.


hah, sounds like its much ado about nothing.


Top
 Profile  
 
 Post subject:
PostPosted: Mon Nov 30, 2009 9:43 am 
Offline
Family Elder
User avatar

Joined: Mon Sep 11, 2006 3:00 pm
Posts: 2197
Location: Dayton, Ohio USA
There are too many people out here with MS who know about this. You can't hide the truth. If it turns out to be the truth it will come out. Informed patients is all we've ever been. Joan took this to Stanford and started a wildfire. If everyone did that, it will eventually come out. Every time someone takes a swipe at CCSVI we just need to calm down and let it play out. Just because he couldn't publish when he wants to doesn't mean that Wayne State and SUNY and others aren't still working on this.

Did we all expect the community at large to just take this at face value and not take any shots? Not me anyway. This has a long way to go as our Doc, GiCi whose had the procedure, often reminds us.


Top
 Profile  
 
 Post subject:
PostPosted: Mon Nov 30, 2009 11:01 am 
Offline
Family Elder
User avatar

Joined: Thu Sep 23, 2004 3:00 pm
Posts: 2066
Location: USA
did you see this thread?

http://www.thisisms.com/ftopict-9021.html

Someone called Elesevier and asked, they said it was coming out this week.

It is easy to get concerned about blocked research, but maybe someone jumped to a conclusion?

I mean to buy this paper--I'd like to think that to do so rewards the publisher for doing new potentially controversial work. Think so?

_________________
I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you...
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics


Top
 Profile  
 
 Post subject:
PostPosted: Mon Nov 30, 2009 11:06 am 
Offline
Family Elder
User avatar

Joined: Tue Nov 24, 2009 4:00 pm
Posts: 222
I think it's good to support the publisher, but I don't see how they would publish it if they thought the science wasn't sound. I don't mean "sound" as in "proof", but as in a sound scientifically-designed preliminary study. If they felt it was contraversial but wanted to publish it anyway, they'd probably have a disclaimer.

Just my two cents..


Top
 Profile  
 
 Post subject:
PostPosted: Mon Nov 30, 2009 11:33 am 
Offline
Family Elder
User avatar

Joined: Mon Sep 11, 2006 3:00 pm
Posts: 2197
Location: Dayton, Ohio USA
Plus,

I hear that all over the internet people are going to start charging more and more. Maybe not true, but I've read articles that allude to that.


Top
 Profile  
 
 Post subject:
PostPosted: Mon Nov 30, 2009 11:58 am 
Offline
Family Elder
User avatar

Joined: Thu Sep 23, 2004 3:00 pm
Posts: 2066
Location: USA
wrong thread :oops:

_________________
I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you...
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics


Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  [ 23 posts ]  Go to page Previous  1, 2

All times are UTC - 8 hours [ DST ]


Related topics
 Topics   Author   Replies   Views   Last post 
There are no new unread posts for this topic. Do any other non-MS people ever have blocked CS veins?

[ Go to pageGo to page: 1, 2 ]

Wonderfulworld

25

4307

Tue Jan 05, 2010 9:08 pm

islander View the latest post

There are no new unread posts for this topic. blocked stent question - w a r n i n g !

[ Go to pageGo to page: 1, 2, 3, 4 ]

bas

54

11348

Fri Nov 18, 2011 9:21 am

Cece View the latest post

There are no new unread posts for this topic. Completely Blocked RIJV

[ Go to pageGo to page: 1, 2, 3, 4 ]

WinnipegGirl_83

48

4955

Thu Apr 07, 2011 8:17 am

munchkin View the latest post

There are no new unread posts for this topic. Treatment in Italy - When?

fernando

6

1521

Sun Sep 20, 2009 8:19 am

spiff View the latest post

There are no new unread posts for this topic. Surgeries in Italy??????

lovebug

4

1881

Wed Jul 14, 2010 4:04 am

joge View the latest post

 


Who is online

Users browsing this forum: No registered users


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

Search for:
Jump to:  


News News Site map Site map SitemapIndex SitemapIndex RSS Feed RSS Feed Channel list Channel list
Read hundreds of personal Multiple Sclerosis stories on Experience Project. Experience Project is an anonymous community where people connect through their life experiences, made by the same people who built This is MS. With over 30 million personal stories about every possible life experience, you can quickly find people like you!


Interesting: Secret Confessions | Dream Meanings | Ask Questions, Get Answers

Advertise on the premier multiple sclerosis forum