A second CCSVI foundation?

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
Post Reply
User avatar
frodo
Family Elder
Posts: 1749
Joined: Wed Dec 02, 2009 3:00 pm
Contact:

A second CCSVI foundation?

Post by frodo »

I knew one at ccsvi.org. It seems that there is a second one:

http://www.ccsvifoundation.org/

anybody knows about them?
User avatar
VeeBee
Family Member
Posts: 42
Joined: Tue Apr 06, 2010 2:00 pm

Post by VeeBee »

Davie Hubbard (VP)
Monica Mulcahy (CFO)
Amber Alstott (pinup)

Board of Directors

Ginger MacQueen
Diana Gordon
Dawn Skinner
Steve Garvie
Yvonne Andersen
Christopher Alkenbrack
Jeanine Baker
Patrick Farrell


No comment.
User avatar
IHateMS
Family Elder
Posts: 168
Joined: Sun May 17, 2009 2:00 pm
Contact:

Post by IHateMS »

Canadian?
User avatar
VeeBee
Family Member
Posts: 42
Joined: Tue Apr 06, 2010 2:00 pm

Post by VeeBee »

440 E Ferry St.
Detroit, Michigan, USA
Tel: 313-758-0065
http://www.healingwell.com/community/de ... &m=1917231

M R I Institute For BIO-Medical Research team foundation
"There's a difference between us. You think the people of this country exist to provide you with position. I think your position exists to provide those people with freedom."

William Wallace (Braveheart) on CCSVI/MS medical Nobles
User avatar
VeeBee
Family Member
Posts: 42
Joined: Tue Apr 06, 2010 2:00 pm

Post by VeeBee »

No rhyme or reason.

I was lead to site via copyscape

hXXp://www.ccsvifoundation.org/faq.php

Im not going to question why a so called professional organization would copy a non professionals content but I'd like to know why they would add links to the equivalent of Colin Rose.

hXXp://www.quackwatch.com/01QuackeryRelatedTop ... ation.html


http://theatlasoflife.com/2010/06/17/th ... uackwatch/


So ccsvifoundation have donation reps everywhere. They have people on this forum but want this nonsense site to slip under the radar.

This foundation walks and talks like a duck, quack quack.

Congrats on running CCSVI into the ground for a few $$$.


Has Ginger Maqueen been vetted?

http://www.spoke.com/info/c1FrULZ/Hp3HealthcareConcepts

Oh, I forgot to mention the deceptive SPAM under numerous names.

Google it using " "

"I was diagnosed with Multiple Sclerosis back in 1983. I can hardly walk now and it seems my condition worsens every day"

CCSVI is an important decision for many and organisations pretending to be running an effective awareness campaign are ripping the piss for profit their own little non profiting way.

It's worked in keeping up demand but is the major CCSVI campaigning a sham? It would certainly help justify prices these good doctors are willing to bump up.
Post Reply
  • Similar Topics
    Replies
    Views
    Last post

Return to “Chronic Cerebrospinal Venous Insufficiency (CCSVI)”