Search Results for "Mito Xantrone"

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This article was written by the neuro I saw in Boston a couple of years ago to get a second opinion on mitoxantrone. At the time my newly dx'ed RRMS was very active/aggressive (serious relapses every few months) and my regular neuro suggested I might need...


Anyone had Mitoxantrone as part of their treatment? if so how well did it work?


I have a friend who has had about 3 treatments of Mitoxantrone, is 42 and has Secondary Progressive MS without relapses so far. Recently His legs have got worse. he has fallen more frequently and once got stuck on the floor and didn't have the strenght ...


Anyone here had any of the chemo therapies to treat secondary progressive ms or any other progressive types of ms? Such as Azathioprine,Cyclophoshamide,Cyclosporine,Methotrexate or Mitoxantrone? I would be interested in hearing how people have respon...


Dear Experts, My Sister has MS and we want your advise regarding the therapy she is advised to take now, below little from her MS history: She took the below medicines in the order given : AVONEX INTERFERONE COPAXONE TYSABRI At this point...


I had removel of my prostate 9 years ago. After 4 1/2 years I started to have a rising PSA again. I had 52 treatments of radiation. (bad stuff). My PSA started to rise again. Dr. put me on Lupron and Casedex. PSA continues to rise. Took me off of cas...


What's the option for an MS patient who is allergic to steroids?Is there any other medicine that will work on any MS patient allergic to steroids in first place?Thanks.


this is the chemo drug that is suggested to people with secondary progressive MS, and it is supposed to help slow down the progression. Has anyone here ever heard of, or taken this drug.??? It scares the be jeepers out of me, and I think it would be a ...


Our 9 yr old Standard Poodle, Monty, was diagnosed with prostatic transitional cell carcinoma in Oct. 2007. He has had a series of 4 IV chemo treatments with 3.7 mg of Mitoxantrone, the last one on 12/31/07. He takes 7.5 mg of Promicam, 15 mg of Pepcid a...


Has anyone here heard of or experienced Uveitis as an initial symptom of ms or had it during their course of ms? I have read it can be related but just wanted to know how common it was.


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