 |
Member
|
|
Join Date: Jan 2008
Location: Southern California
Posts: 308
|
|
Member
Join Date: Jan 2008
Location: Southern California
Posts: 308
|
Yay Victor! Sorry Sheena
Yay Victor on getting the cost of your Ty down. What they were charging you is ridiculous! I believe mine is costing me about $520 a month...which is high. Amazing, I have friends who have Kaiser...they pay NOTHING for their tysabri! Craziness.
Sheena - sounds like you're having a rough ride from your infusions. I do hope your doctor will talk to you about all of your options if he does decide to stop the Ty. Sad you're having bad reactions. The first 5 days after Ty, I can barely move - so "exhausted" thought it's unlike the other MS fatigue....hard to explain, but I feel like 5000 lbs of lead are on top of me.
Supposed to go for second Ty on May 9 - but am reconsidering as I am now in talks with Johns Hopkins about that treatment...
~k
|