CCSVI Calgary was created for people in the Calgary area who are pro-active in getting CCSVI testing and treatment available in Alberta. We are a grass roots group who hold regular meetings, plan activities, rallies and campaigns, and by working together we are spreading the word about CCSVI in Multiple Sclerosis.
In July, 2010 we incorporated as an official non-profit organization.
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For details on how to help us or donate to the cause visit How To Help.
Contact us: info (at) ccsvicalgary.org
Phone: (403) 874-6480
Mailing Address:
CCSVI Calgary
P.O Box 221
104-1240 Kensington Rd. NW
Calgary, Alberta
T2N 4X7
What we want:
MS continues to attack you, and some people don’t know that. It’s not a disease that you get and stays the same, You get MS and you get worse. Waiting five years can change people’s lives. They might not be able to work. They might not be able to take care of their children. They might not be able to take care of themselves. This is why waiting 5 – 10 years is unacceptable. And we don’t want to go to other countries for it. We want the testing and treatment done here.
There’s enough evidence from the initial trials to demonstrate there is a relationship between MS and CCSVI also between the level of disability and CCSVI. This procedure would cost less than half a year’s worth of medicine for many of the more advanced patients. In the cases where blockages are found, even if it was only 50% of MS patients in the province, the results are too good to ignore.
The information discussed on this website is in no way meant to replace professional medical advice or treatment. For symptoms, questions and medical advice see your medical doctor.