Guest guest Posted September 29, 2004 Report Share Posted September 29, 2004 I think I know who you are talking about. I met him years ago when I was involved with an organization for pseudoobstruction. We treated Max as if he had it when he was a baby because there was nowhere else to go. And it was a great organization, but I think they are more into Hirschbrung's now. I would love to hear someone else's take on the dysmotility/gi issues that our kids face. I know that we are pretty frustrated because we have had Max go through the " triple procedure " and his reflux is getting worse. Fundos do loosen in time, but in just a year???? He is now taking Cisapride for the dysmotility, Protonix as a PPI and Prevacid in the afternoon. Then I found out today that he goes to the nurse several times a week for Tums. Oy! Jodi Z. Quote Link to comment Share on other sites More sharing options...
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