My doctor recommended Rituximab, claiming that it is more effective than interferons and is less expensive. However, when I look up the negative effects on the internet, they appear to be quite frightening. So I'm hesitant to begin this medication, especially during this COVID time when immunity is so vital.
I would suggest trying Rituximab. When I started Ritux, I had given up DMD's in general but 2 days after taking my first infusion I could tell I had found my DMD. Almost any listed side effects for drugs aren't fun and a reasonable person would never take any drug but you will never know if you will experience some or none of the sides unless you try. I don't know if Rituximab is the drug for you but we'll never know unless you try!
I took rituximab for two years. The side effects are scary the rare fortunately. Many find it effective. I did for first year.
I've been on Rituximab for over ten years. It has been working well for me... I did drop in my blood counts , but I now also get IVig treatments and that has been solved.
I have taken Retuximab for about 2-2 1/2 years. I started with Gilenya. There’s been no MS progression with Retuximab and I’ve remained lesion free. My doses have been twice a year and now this year they will start as once a year. This way I can remain on it longer. We can’t be on one DMT forever-I just don’t think it’s possible. Retuximab is basically Ocrevus-just labeled different. Look that up!