CCSVI Research Transparency web site : Chronic Cerebrospinal Venous Insufficiency (CCSVI) - This Is MS Multiple Sclerosis Community: Knowledge & Support

View unanswered posts | View active topics

Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

All times are UTC - 8 hours [ DST ]

CCSVI Research Transparency web site

Page 1 of 1

[ 1 post ]

Print view

Previous topic | Next topic

Author

Message

bohemianbill

Post subject: CCSVI Research Transparency web site

Posted: Sat Nov 28, 2009 9:48 am

Family Member

Joined: Fri Nov 27, 2009 4:00 pm
Posts: 81

Dear friends My wife has been afflicted with MS for 20 years now, wheel chair. WE live in canada and last week you may be aware that our national ctv w5 presented "the Liberation Treatment" CCSVI. Needless to say it has stood the canadian MS population on its head.

I/WE believe that due to the amount of Money involved in the Business of MS CCSVI has a difficult fight on its hands.

We further believe that 100% Transparency of the research to be conducted & funded by the www.mssociety.ca is Critical.

Therefor i am inviting you to please go to

www.ccsviresearchtransparency.com

your participation is greatly appreciated

-keep the heat to the feet-

Top

Page 1 of 1

[ 1 post ]

Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

All times are UTC - 8 hours [ DST ]

Topics		Author	Replies	Views	Last post
Related topics
	Non-mainstream MS Research: CCSVI, LDN, CAMNMO research etc.	Neurologique	0	933	Mon Nov 01, 2010 5:42 pm Neurologique
	Question about incision site for CCSVI	Boopieup	9	1521	Mon Oct 12, 2009 1:15 pm LR1234
	CCSVI RESEARCH here [ Go to page: 1 ... 8, 9, 10 ]	mrhodes40	146	76855	Tue Jun 11, 2013 1:18 am squiffy2
	CCSVI -- why we need more research	Rosegirl	1	1350	Sun Mar 07, 2010 8:56 am jean-la-grenouille
	CCSVI Research Funds	Needled	0	1055	Sun Oct 18, 2009 11:44 am Needled

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

Jump to:

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

This site does not offer, or claim to offer, medical, legal, or professional advice. All treatment decisions should always be made with the full knowledge of your physicians.