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I am a caregiver for a father with PPMS; currently we are on various lists for the CCSVI procedure. My father took part in the screening at BNAC where it was confirmed that he has CCSVI in his main right jugular and is missing his left altogether.
I am reaching out to hear any stories of people who are quadriplegic from MS who have had this treatment done. I am interested in everything: you plane rides, the doctors, the improvements, everything.
I would be grateful for your stories.
