I was diagnosed with WM last year. My hematologist recommended Rituximab because it would also alleviate my neuropathy issues. I said no. Three months later he again recommended the Rituximab and I went ahead. I met with medical team who prepared me for the procedure.
I had four infusions a week apart. The first left me very tired but I did not need the anti-nausea meds they had given me. The next three sessions went fine with no side effects and it did help with the neuropathy pain. After the last am treatment I went to a movie that afternoon.
Doctor wanted the next round six months later so that’s coming up soon. I do not expect any problems this time either, hoping again for further pain relief.
I also have myelofibrosis and have been taking 500 mg of Hydroxyurea daily for two years. I continue to be active and enjoy all my usual activities.
I will not let my cancer define me. I let my faith and attitude do that.
I pray that all goes well for you, too, my friend. 🙏🏽👍🏼