Quote:
Originally Posted by SallyC
How are you all feeling day to day, on Tysabri. Especially those who have been on it for over a year or two. Have your MS sx deminished, gone away, a little better, a lot better or NOT?
Do you have side effects from the TY and if so, are they really managable? Do you have the JCV antibodies? Are you afraid to take TY, but because of your great results, you are willing to take the risk?
I hope you don't mind my asking. I think about you all often and come to read here, to see how you are doing, but usually, your just counting off your infusions. How do you really feel?  |
I'm doing awesome on Tysabri. I've had my diagnosis for ten years. I started taking Ty four years ago. My fatigue is largely gone, my strength has returned enough for me to train a horse, work, raise my daughters and separate from a marriage that had become abusive. On the rare occasion when I remember to pray, I thank god for modern medicine and for Tysabri and for the full and vital life I've been blessed with.
Katty