I'm creating this blog for my family and friends, in hopes that is may help them if they find themselves in a similar situation. Once I've obtained treatment and recovery from CCSVI, I'll be sure to let other people know about it, and spend the next few years lobbying for more accessible treatment centers in the US and beyond. Currently it is being treated in only 7 states. I am also hoping for a streamlined path to obtaining insurance coverage of "The Liberation Treatment". Because of the degenerative nature of the condition, time is especially valuable. If you suspect you have problems associated with reduced flow in veins, take action as soon as you can.
Family is first for me, and friends are family you choose. This is for the ones I love.
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