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    Rituxan

    I have noticed a few others are taking Rituxan for MS. I have been given this option and I am seriously considering it....

    Of course I have a few questions....

    Has anyone gone from Tysabri to Rituxan? Any relapses or issues coming off Tysabri?

    My neurologist is suggesting, one 1,000 mg dose ever six months. Is this how the drug has been prescribed for your use? Or did you do a dose two weeks apart and then every six months?

    How many infusions have you had? Any side effects?

    Did anyone get their insurance to cover the cost of the drug?

    Any other information you can share about your experience would be greatly appreciated.

    For those in CA, where in the state are you?

    Thanks in advance

    KSL

    #2
    I'm speaking up so that I can find this thread again. My new neuro told me he suggests I switch to this med as well; I see him again in early August to discuss.

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