Hi all, I've been hovering these pages for a few months. I should introduce myself, I'm a Canadian living in Houston Tx. Diagnosed at age 26, but probably had first attack at 17. I'm 46 now and I'm starting to feel defined by the disease. It creeps into every thought. I'm sure this is understood by many of you. My father also has MS. The CCSVI discovery has given me strenght and has recharged my attitude.
Thankyou to Cheer and everyone who has given so much. It feels so good to know you are out there.
Jo-Ann