Introducing myself after reading some 10 pages out of 56 page discussion on CCSVI (my latest research of interest) - this board is full of very knowledgeable people!
I am 39yo mom of two, engineer and a part time student.
Briefly about my MS - Dawson fingers on the brain, big sclera in the tail bone region. Only had one initial round of MRI's, about five of them.
Since then tried many alternative therapies (I refused conventional drugs), right now settled on Best Bet diet, including recommended supplements, B3 flush twice a day, apitherapy and yoga.
Since I did not have a follow up MRI since initial diagnosis I was never labeled to have RRMS ot PPMS.
All I know, I was accumulating new symptoms with high speed for several months until I started implementing above strategies.
Now, I had no new symptoms for 1.5 years, my fatigue is greatly reduced, my speech is back to normal, my shoulder spasms are gone.
I still limp (mostly left leg), feel inflammation in my "transmission" and have leg spasms, especially in the morning.
I do not have "attacks", nor do I have remissions.
Looking forward to learn as much as I can from all of you!
<strong><strong>MSIS-29 = 88</strong></strong>