cytoxan therapy

A board to discuss Revimmune as a potential therapy for multiple sclerosis
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Re: cytoxan therapy

Post by Pookie » Sat Feb 18, 2012 3:20 pm

My husband had low dose cytoxan a week and a half ago. Every eight hours with steroids. He has SPMS. He was in the hospital for 3 days. He did well the day after he came home. Then it went downhill. Weakness - lots of weakness. Plus his trigeminal neuralgia came back. I ave been home with him the past week and will take the next week also. Does anyone know ha long it will take to Regina strength? Thanks. Marlene

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Re: cytoxan therapy

Post by Lyon » Sat Feb 18, 2012 3:47 pm

Hi Marlene, you might want to also post your question to the general forum because people who have experienced low dose cyclo would be more likely to notice it there.

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Re: cytoxan therapy

Post by LauraV » Mon Jul 02, 2012 9:54 am

Is there much difference between MS cytoxan therapy and the cytoxan therapy they give for breast cancer? I took cytoxan with adriamycin (and steroids) for every two weeks for eight weeks as the first part of my chemo for breast cancer. I noticed my MS symptoms worsening. Saw a neuro recently and was shocked to find out that cytoxan was considered therapeutic for MS.

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