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Posted by stephensaffhill on July 9, 2007, 4:32 am, in reply to "Re: Freq. relapse/Steroid dependent TAPER Question" I'm very happy to say that she has been in remission and off all meds since then. However we are under no illusion that there will not be another relapse and continue to test for Protein every other day. Of course, we remain positive & are grateful for every day that she is clear. Best wishes & hope the Cyclophosphamide works for your son. --Previous Message--
130.32.42.1
Hi, my daughter completed an 8 week course of Cyclophosphamide in June 2006. During this period she was also weened of Pred and finished about a week or so before she finished the course of Cyclophosphamide. She also had to go for weekly blood tests during the period.
: My son, now 7 and 1/2, was diagnosed with MCNS
: in October 2006. He responded to
: prednisolone (steroid) and was being tapered
: off when he relapsed first time in Feb. He
: went back up to the full dose and was being
: tapered when he relapsed again in May. He
: has steroid dependent MCNS.
:
: We noticed that he has relapsed both times
: when the dose went down by 0.5 mg/kg
: increment (from 1.0 mg/kg to 0.5 mg/kg
: during 1st relapse or from 1.5mg/kg to
: 1.0mg/kg during 2nd relapse). We are working
: with his nephrologist to go slow (in
: increments of 0.25mg/kg) during the current
: taper schedule.
:
: We are concerned that he may relapse yet
: again. His nephrologist has mentioned
: Cytoxan (or Cyclophosphamide) should there
: be future relapses.
: Can Steve or other people share experiences
: of their children being initiated on
: Cytoxan....it will help us on what to
: expect.
:
: Thank you
:
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