cytoxan therapy

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

Re: cytoxan therapy

Postby Pookie » Sat Feb 18, 2012 4:20 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
User avatar
Pookie
Getting to Know You...
 
Posts: 17
Joined: Sun Oct 01, 2006 3:00 pm

Advertisement

Re: cytoxan therapy

Postby Lyon » Sat Feb 18, 2012 4:47 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.
Lyon
Family Elder
 
Posts: 6063
Joined: Wed May 03, 2006 3:00 pm

Re: cytoxan therapy

Postby LauraV » Mon Jul 02, 2012 10:54 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.
User avatar
LauraV
Family Member
 
Posts: 65
Joined: Mon Jun 14, 2010 3:00 pm
Location: NY

Previous

Return to Revimmune (cyclophosphamide or cytoxan)

 


  • Related topics
    Replies
    Views
    Last post

Who is online

Users browsing this forum: No registered users

cron