Just a quick note (I'm fighting the Avonex crud tonight) My friend here who was in a wheelchair just a year ago from ms is now on Tysabri (she was on Avonex and novantrone and got good results) and had her 3 mos. neuro check and mri...her neuro is amazed, he says her mri is clear, if he hadn't known her all this time he would say she doesn't have ms! Her walking, etc..is so much better. She has progrssive relapsing, very rare. On Tysabri you have to have an mri and neuro appt. every 3 months.
My hubby wants me to go on the Tysabri but we'll see what my neuro says in march. She doesn't want to change anything right now (she won't even change me to the powder avonex).
Also, I had my anal manometry today and it wasn't painful, I think it was normal and I will probably see the gi doc next wed. I will see a new urologist on Monday.
Take care...big hugs to all of you who aren't feeling well or are emotionally hurting.
Co-Moderator MS forum
Happiness is not a destination but a day-to-day journey..
Post Edited (shellypoo) : 2/14/2007 8:14:32 PM (GMT-7)