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    #16
    Originally posted by Pomegranate View Post
    I went from having to use a cane or a wheel chair for moderate to long distances and now I use nothing. I've only had one relapse this year, which is great for me.

    .
    May I ask how long it took for you to start feeling positive results from the treatment? I am two weeks post my first infusion and I feel like poop. Muscle weakness and worse fatigue. My MS specialist told me it is normal to feel worse. I'm wondering when I go from feeling worse to feeling my normal level of crappy to potentially feeling better :-)

    Thank you and I'm so glad you found something that has made such a huge difference in your life!!
    Melissa Goerke
    [I]DX 7/2/10, Copaxone then Avonex, started Ty 9/13/11, JCV+ ended Ty 9/13, started Gilenya 12/13 Blood Pressure skyrocketed, started Tecifdera 4/5/14 - fatigue beyond bearable and symptoms became worse. Rituximab 8/8/14.....waiting for the miracle. I WANT MY TYSABRI BACK!!!

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