Hello everyone!
Yesterday I finally started this treatment for 4 weeks to go along with my IVIG. I was informed that it will take several months for me to feel the effects. I’m hoping that this will help until I find out about the SCT.
I want to be clear, I as well as others to my knowledge do not act like victims to this very aggressive disease, I just feel that we have been through a lot and know that this disease is not to be taken lightly and we will do anything to feel better.
That’s that for my rant on that.
I hope I get to feel a little better soon, today I feel very sensitive in my legs and feet, a little stiff.
Has anyone else have this and what and how did you feel afterward?
Hi, Paula, I just saw your post from last year. How did rituximab work out for you?
This treatment has been suggested to me as well. I have to make a decision this monday. I havent read anything positive about it all all. I would like to know if anyone else has had any luck with it
dancermom said:
Hi, Paula, I just saw your post from last year. How did rituximab work out for you?