This Is MS Multiple Sclerosis Knowledge & Support Community

UPDATE: Hubbard Foundation will begin to do one trip scanning and treatment starting mid september. We will still need an MRI prescription/requisition, and BUN and Creatinine blood levels. We're going to finish treating those we've scanned and those we've scheduled to scan, but send us your contact ...

Hubbard Foundation update:
5th patient treated today
6 more being treated next week
6 more scheduled for treatment over the next weeks as the patients' schedules allow

CCSVI TRACKING 05/17/10 MS HISTORY Devin Hubbard Male/Female: M Age: 27 Date(s) RRMS Lesion locations (most affected side, if known), number: MS treatments: Rebif, gluten/dairy free diet, supplements like vitamin D and Nattokinase MS symptoms before stenosis intervention: double vision, facial paral...

on both jugulars and my azygous. No more brain fog or fatigue. No more double vision. Feel so good! I want this for everyone.

Hubbardfoundation.org for more info. My father, Dr. Hubbard, a neurologist set this up when I was diagnosed with MS in December. Now we just want the same peace of mind for my fellow MSers and their families. Hope this helps.

My father, a neuro, tried to get me into a study and couldn't, so he started scanning the haacke protocol down here, and found an IR to treat me. We should be referring patients for the venoplasty by mid june. hubbardfoundation.org. Hope this helps.

Had the balloon angioplasty on May 7th. Brain fog gone, fatigue gone. My father, Dr. Hubbard, is a neurologist, and after my mom started researching CCSVI, dad started looking into it too. We couldn't get me into a study fast enough, so dad set up screening Haacke Protocol Screening test in San Dieg...