IVCC/CCSVI, vidéos et échos de murs de ce dimanche.

Publié le par Handi@dy

Barre google de traduction indispensable.

ccsvi-faces-of-Liberation2.jpg

*

My wonderful son the MS fighter!

*Echos de murs:

*CCSVI at UBC MS Clinic - Information and Support  Sixty days MS free -- oh what a feeling!

*François Leclair
LES RÉSULTATS DE MA CHIRURGIE !

Actuellement, je suis au repos et je constate quelque peu les changements qui s'installe en moi. Par exemple, mains et pieds plus chauds, brain fog (nuage de fatigue) n'est plus présent et la vessie est moins active. Pour la marche, je vais devoir faire beaucoup de physio. Le plus important de cette chir...urgie est qu'on arrive à stopper le processus de dégénérescence.
François Leclair OPÉRATION A ÉTÉ UN SUCCÈS ET SANS COMPLICATION POST-OPÉRATOIRE !

La jugulaire gauche était sténosé (rétréci) à 60% et la droite avait un problème au niveau du débit du flux sanguin dû aux malfonctionnement des valves. J'ai dû avoir deux balloning (angioplastie) à gauche et une à droite. L'opération a durée 1:30.

*Bilal Abdul Kader  Greetings,
I have registered an idea at AVIVA community fund asking for a grant for CCSVI trials financial support in Canada (http://www.avivacommunityfund.org/ideas/acf8942). Can you please help me spread the word. We need about 500 people ASAP to get to the semi-final round and I am sure this is achievable.

It takes 30... seconds to register and vote. Each person has 10 votes (1vote/day) and we need about 5000 votes to make it. It is about 500 people only.

*Ken Torbert  Need an idea for a Halloween costume?Be "MS" or a "Constricted Vein" Have
fun and be creative with an MS-themed costume. You'll be spreading
awareness about multiple sclerosis while you assure friends that,
despite how SCARY this disease can be, the BNAC research team is hard at
work learning more each day about MS.......Email photos to Lsafran@bnac.net for possible posting on our Facebook page.

*Tessa Rushton
passed the good word onto a lot of great people today! thanks to the MSS of Calgary for setting CCSVI Calgary up with a table. Met a lot of new friends today... nap time - gotta get some energy for the CCSVI Calgary HALLOWEEN party tonight :) boo!

**Michelle Walsh
is telling everyone she knows "Venous Angioplasty For all in Canada whether you have MS or not. Stop the discrimination and if you believe in this too please help us you can donate as little as the cost of a pizza a month $20 www.angioplastyforall.com this will help cover legal fees to fight this in CANADA right now everyone.

Michelle Walsh  via Sarah Rainbolt : Thank you for Dr Paulo Zamboni for doing this
Inventor of 'liberation' treatment for MS blasts skeptics in Alberta government
www.montrealgazette.com

*Amy Gaylord-Preston
The ignorance involved in preventing proper blood flow now, in a system of "Universal health care" is baffling." What are our provincial and federal leaders thinking?




Commenter cet article