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Sequential maintenance treatment with glatiramer acetate after mitoxantrone is safe and can limit exposure to immunosuppression in very active, relapsing remitting multiple sclerosis.
Mitoxantrone as induction treatment in aggressive relapsing remitting multiple sclerosis: treatment response factors in a 5 year follow-up observational study of 100 consecutive patients
I appreciate the post and Revimmune sounds like the ticket for the people I've read about. Here's the thing, I'm SPMS with no currenly active lesions and I'm about a 7 on the EDSS scale. I'm sure I'm not what Hopkins is looking for.
Thanks and all the best with the therapy
I share your concerns. Novantrone is not a cure nor is it a viable long term treatment. Therefore, treatment with Novantrone alone may not be the best option available. Though, some studies, such as the ones that Dignan has provided links for, have shown increased benefit when Novantrone is combined with subsequent treatment with Copaxone. After doing some investigation on your own, I would recommend that you then discuss your concerns with your neurologist.digepix wrote:Now I know about the heart toxicity and the fact that Serono makes no guarantees that a year or more after stopping Novantrone you wont have heart problems. So what's the upside? It may or may not stabalize your MS? So after you stop Novantrone you remain stable for one month, one year. It seems like alot to ask someone to agree to with little or no lasting value. So please help me to understand the benefits so I can formulate my own risk/reward profile.
I was DX'd in Oct 05, on Betaferon Nov 05, going downhill fast, and on Novantrone Aug 06. Just finished the two years and all I can say is do it. Everyone is so scared of the word chemotherapy, and the stories associated with it. Fact is Neuro's are going to recommend patients to go on it unless they believe it is necessary and will help.
I didn't see the miracle recovery, that everyone hopes for, and don't get, but no one can argue with the significant improvements shown in my MRI's as a result of being on Novantrone. You, and anyone with MS, has got nothing to lose by trying it, but you've got a hell of a lot to lose if you don't.
I hope all goes well. My time on Novantrone was notable for it's lack of trouble and drama, just the way I prefer things to be.
But I'm not worried, I figure if LDN is good at treating canser, maybe it will prevent it too.
Why would anyone consider these posisons, look into the CCSVI treatment, there's a big thread on it here. Now there's Dr Haake http://www.ms-mri.com who is proposing this quickly become a standard of care for MS, skip the research loop and just document the results on those who are lining up to get the procedure. I already have my appt at Standford.
But I will always stick with LDN, for cancer protection, and just to buffer my immune system that has been so battered by the MS drug industry.