Support The Liberation Procedure (The Zamboni Procedure) in Canada
New research conducted by Dr Zaboni in Italy has shed new light on this nightmare disease, for decades it has been believed that MS is a autoimmune disease but Zamboni has proved that it is actually a vascular disease. Over 500 MS patients have been tested and all have shown deformities in their Jugular veins. No one in the control groups had the deformities.
Doctors in Italy, The US and Poland have carried out procedures on dozens of MS patients, where stents are placed in the Jugular veins to allow the free movement of blood to the brain. Those who have undergone the procedure report miraculous improvement in their condition.
WE WOULD LIKE THE CANADIAN GOVERNMENT TO EXPEDITE THE APPROVAL TO USE THIS TREATMENT. TIME IS OF THE ESSENCE. If you or someone you know has MS please, please sign this petition.
International Petition open to all – http://www.gopetition.com/petitions/the-liberation-procedure.html
Support The Liberation Treatment/CCSVI Research in the United States
New research conducted by Dr Zaboni in Italy has shed new light on this nightmare disease, for decades it has been believed that MS is a autoimmune disease but Zamboni has proved that it is actually a vascular disease. Over 500 MS patients have been tested and all have shown deformities in their Jugular veins. No one in the control groups had the deformities.
Doctors in Italy, The US and Poland have carried out procedures on dozens of MS patients, where stents are placed in the Jugular veins to allow the free movement of blood to the brain. Those who have undergone the procedure report miraculous improvement in their condition.
WE WOULD LIKE THE U.S. GOVERNMENT TO EXPEDITE THE APPROVAL TO USE THIS TREATMENT. TIME IS OF THE ESSENCE. If you or someone you know has MS please, please sign this petition.
International Petition open to all – http://www.gopetition.com/online/32789/sign.html
MS-CCSVI-UK UK e-Petition
Independent Petition submitted by Colm McLaughlin – Deadline to sign up by: 01 March 2010
We the undersigned petition the Prime Minister to To make CCSVI procedure available in the UK.
UK Petition open to UK Nationals only – http://petitions.number10.gov.uk/CCSVINOW/
Support CCSVI Research in Australia
This Petition is to get CCSVI researched in Australia and to help the 20,000 people in Australia with MS.
This petition will go to the MS Society of Australia, The Prime minister of Australia, The Health minister of Australia and to who ever will listen. Thank you for your time with this fight to help your follow Aussie’s
International Petition open to all – http://www.gopetition.com/petitions/support-ccsvi-research-in-australia/sign.html
Support CCSVI Research in France
La S.E.P. (Scérose en plaques) maladie auto -immune, se traduit par une dégénérescence du système nerveux central et/ou périphérique (cerveau, moelle épinière). Elle revêt différentes formes. Cependant, pour toutes, à plus ou moins long terme, cela se traduit par une perte du contrôle et par conséquent de l’autonomie de la personne. Ces atrophies, infirmités pèsent lourd également sur l’entourage proche.
La médecine n’a cessé de progresser pendants ces 30 dernière années : interférons, tysabri, endoxan, mitoxantrone… La réponse classique et universelle de la corticothérapie a malgré tout, ses limites.
Une nouvelle approche de cette pathologie qu’est la S.E.P, est en France, ignorée ou laissée sans étude : la C.C.S.V.I. (ou Chronicle CerebroSpinal Veinous Insufficiency). Elle (C.C.S.V.I.) est une condition dans laquelle le sang provenant du cerveau et de la moelle épinière, rencontre des difficultés pour aller jusqu’au cœur. Cela est dû à des sténoses (un rétrécissement) dans les veines qui drainent le cerveau et la moelle épinière.)
Nous, citoyens français, interpellons pouvoirs politiques, scientifiques, économiques, pour qu’une étude sérieuse de cette thérapie soit entreprise en France !
For more petitions see:
http://www.msrc.co.uk/index.cfm?fuseaction=show&pageid=2962&CFID=3314547&CFTOKEN=77716951
