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    #61
    Originally posted by Virginia View Post
    I was thinking of asking Doctor about it when I see him next month, but sounds very complicated. Maybe if I got into it I might feel differently.

    I am going to ask if he thinks I can tolerate Rituxan.
    Virginia,
    Rituxan has almost no side effects for most people who take it. It is one of the safest drugs available to us. Really, it is not complicated. Infusion centers have very competent nurses. Don’t worry.

    Some of us took IVIg and that is what we were talking about in terms of infusion rates. Even then, it is a matter of turning the dial up or down....again, don’t worry.
    Last edited by Lazarus; 06-17-2018, 03:01 PM.
    Linda~~~~

    Be the kind of woman that when your feet hit the floor each morning the devil says:"Oh Crap, She's up!"..

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      #62
      Genentech announced a couple of days ago that they now have 4 cases of PML with Ocrevus. All were on Tysabri and JCV+ and became symptomatic after first dose of ocrelizumab . Here is a link to the announcement. Only registered and activated users can see links., Click Here To Register...

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        #63
        For some reason that link isn't cooperating but the link in the other thread is OK. Here it is, and it's to a .pdf file.

        Only registered and activated users can see links., Click Here To Register...
        SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

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          #64
          Scheduled for July 23. Fingers crossed it does something this time.
          Be the person your dog thinks you are

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            #65
            Good luck, Ssusan! I hope you get an energy boost that lasts.

            ANN
            There comes a time when silence is betrayal.- MLK

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              #66
              My infusion is next Tuesday the 31st,, at 7 am,, here at Unity Point Fort Dodge,, so glad I found this neuro,, then a busy week a head of me,, with company/family reunion/and a wedding,,but I'll handle it..
              " Don't outsmart your common sense"

              Peg

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                #67
                Keeping fingers crossed for you, Peg. With a schedule like yours for that week, I'd be chickening out on some of those public appearances. I admire those who soldier on.
                SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

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                  #68
                  Peg, what a week coming up. Hope you haven't volunteered to cook. Good luck with your Ocrevus infusion. I can't remember if you ever got to take the first two half doses and this is your first full one or if you never could get it scheduled at all. Hope you get a good boost of energy and some good lasting effects.
                  Virginia

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                    #69
                    ssusan must have had an infusion yesterday. Hope that went well.
                    SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

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                      #70
                      Peg, good luck. I don’t know how you do it!!

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                        #71
                        Originally posted by Virginia View Post
                        Peg, what a week coming up. Hope you haven't volunteered to cook. Good luck with your Ocrevus infusion. I can't remember if you ever got to take the first two half doses and this is your first full one or if you never could get it scheduled at all. Hope you get a good boost of energy and some good lasting effects.

                        its my 3rd time with this,, and I really am seeing results with it
                        " Don't outsmart your common sense"

                        Peg

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                          #72
                          That’s good news, Peg.

                          ANN
                          There comes a time when silence is betrayal.- MLK

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                            #73
                            Peg, that's great news! Keep it up!
                            "Given the millions of billions of Earth-like planets, life elsewhere in the Universe without a doubt, does exist."

                            Albert Einstein

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                              #74
                              While reading this thread I'm reminded that I'm almost 2 months late for my next Rituxan infusion. Falling and getting a concussion with amnesia can do that to a person. Tomorrow marks 9 weeks since my fall.

                              There are no general neuros that take my insurance within 70 miles of where I live. The MS specialist I see is 75 miles away. I better call his office about scheduling my next Rituxin infusion.
                              s
                              Jendie
                              I've been a member of this forum during its different incarnations since I was dx in 9/98

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                                #75
                                Jendie, you've been through an ordeal. Not too surprising that the Rituxan infusion had to be delayed but what a shame that the doctors are so remote from you.

                                How have you been doing?
                                SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

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