

*NOTE* You must register to use this board. All posts will be reviewed before being posted. This is done for your protection and to stop spammers with nothing better to do with their time. Your post will usually show up within a few hours.
Posted by dscmvalentine
![]()
on October 14, 2007, 4:15 pm
65.255.238.21 | Message modified by user dscmvalentine December 7, 2007, 11:32 am
My 22 month old son was just diagnosed with MCNS and we are just starting treatment with prednisone. The information we received is quite overwhelming and it seems it can be a wait-and-see game with the severity and frequency of relapses. If any of you are in the same situation I would love to hear from you.
valentine@harewaves.net
Message Thread:
![]()
« Back to thread
Please consider
supporting our mission Kidcomm is an
online resource for parents of children with nephrotic syndrome and other kidney
diseases. Your donations help keep Kidcomm, it's email support groups and this
bulletin board up and running. Please consider donating in
order to help us help you. Click
here if you would like to donate
Vist our home site Kidcomm - An online resource for Parents.
Join one of our private email support groups for parents and kids!
See our selection of books to help you cope!
See our selection of books to help your child cope!