While I was getting my Tysabri Infusion we met a man and his wife who came in to say hello the infusion nurses. He said he would be back next week to start year 2 of Campath.
I asked if he thought it helped and he said definately, although he still could not tolerate the heat and humidity at all. He was excited to have year 2 infusions.
The infusion nurse also said they we giving off label as long as insurance would approve.
Cat
Meet a man starting 2nd year of Campath
Meet a man starting 2nd year of Campath
Holly - Shine On You Crazy Diamond - Pink Floyd
9/3/09 Stanford - Dr Dake - Stent in R-J to unblock Arachnoid Cyst in Sigmoid Sinus. Stent in narrowed L-J. Balloon in narrowing where R & L Jugulars meet.
9/3/09 Stanford - Dr Dake - Stent in R-J to unblock Arachnoid Cyst in Sigmoid Sinus. Stent in narrowed L-J. Balloon in narrowing where R & L Jugulars meet.
I am 4 months post infusions, and while I don't feel miraculously cured, I never expected to. I now am looking at ms as a chronic illness, and my current tx (campath) has left me feeling better than I have in at least 10 years. I will definately go for the year two infusions.
And it sure beats shooting up daily!!!
And it sure beats shooting up daily!!!
Hey Q,
Right now they are just trying to stabilize my platelets. The prednisone has worked and now I am back solidly inot the normal range ~210k. Thing is I can not continue the prednisone for too long and who knows what will happen when I reduce and wean off the stuff. Future treatments for Ms are totaly up in the air. I can not have more CAmpath, which totally sucks since it has been a neurological success to be sure. I do not even know if I can have Tysabri since ITP is on the side effect list for that too. The interfeurons stopped working for me, so where else can I go, what can I do for treatment? I am really stressing about it as I really wish I could continue the Campath. I think I would have been ok with the low dose, but that high dose was too much. It was clear when I was getting it as evidenced by the massive rash, shortness of breath etc.
For now I will just try to enjoy the ~6 months of whatever benefit the remaining Campath in my system gives me...
G
Right now they are just trying to stabilize my platelets. The prednisone has worked and now I am back solidly inot the normal range ~210k. Thing is I can not continue the prednisone for too long and who knows what will happen when I reduce and wean off the stuff. Future treatments for Ms are totaly up in the air. I can not have more CAmpath, which totally sucks since it has been a neurological success to be sure. I do not even know if I can have Tysabri since ITP is on the side effect list for that too. The interfeurons stopped working for me, so where else can I go, what can I do for treatment? I am really stressing about it as I really wish I could continue the Campath. I think I would have been ok with the low dose, but that high dose was too much. It was clear when I was getting it as evidenced by the massive rash, shortness of breath etc.
For now I will just try to enjoy the ~6 months of whatever benefit the remaining Campath in my system gives me...
G