Today is May 26, 2010 and World MS Day. I have been reflecting on the last 6 months since I heard about CCSVI and just about 2 months since I had the liberation treatment. What strikes me is how many folks who have been liberated are still in the trenches fighting for CCSVI scans and treatment in the US and Canada. I have never heard of this phenomena before with any other treatment or drug therapy for MS. Dr's Simka and Ludyga in Poland have treated over 300 patients for blocked veins now and many more vascular surgeons are jumping on the CCSVI bandwagon all over the world.
Why does the government ignore it's people and their rights to have blocked veins treated regardless if they have MS. We are not fighting to have the medical professionals and government recognize CCSVI as the sole cause of MS. NO! We want to be treated for blocked veins that are responsible for draining the blood from our brains back to our hearts. That is all. SO why then are we forced to wait for years for research and clinical studies? When they started doing angioplasties back in the day, no clinical trials took place. They just started doing them.
Canadians and Americans need to educate the government and health authorities about CCSVI. They need to know that no blood flow is BAD. Regardless of any pre-existing conditions an angioplasty is the answer. Again, I want to reiterate that CCSVI is probably not the sole cause of MS but it certainly seems help a lot of people.
Please help spread the word about CCSVI by writing to your local government officials and health care. Make a You Tube video of yourself before and after treatment and hold demonstrations and educational seminars. We must keep the pressure on and build awareness until CCSVI are the 5 letters that are ingrained in everyone's brain across our countries.
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Ginger you are so right, the desision is now
ReplyDeletein the hands of our Government to push this through. My husband put a CCSVI package together attached with a letter to both our Federal and Provincial MP's asking for their help. Today our Federal MP returned our call and said he has had others asking as well and he is going to arrange a meeting with the Health Minister next week to discuss the matter.
We express our concern about opening my viens which I also found out last week were blocked.
If everyone was to take action now and contact their local MP it would have a huge effect. Kas
Thanks Kas. I am also filing a complaint with the Alberta Human Rights Tribunal and need names and contact info of Albertans who have been refuse scanning and/or treatment for CCSVI because they have MS.
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