mitoxantrone /novantrone anyone on this?

Hi.saw my neurologist today and he said if I wanted to change treatment(as I don’t think rebif working) the next treatment he would offer is mitoxantrone or novantrone.obvs strong chemo treatment with serious side effects. Has anyone been offered or been on this?

Thanks

Coleen

??? :frowning: not a drug used by many? Y has my doc suggested it? Confused!

Thats a bit heavy duty why not offer Tysabri or Gilenya next?

My neuro offered me several options one of which was to speak to the Campath trial team but I declined and said I would consider it if things still worsened. He then said that if he were in my position he would be choosing Gilenya which was the option I was leaning towards anyway. Been on it since November and doing nicely.

Tracey x