Guest guest Posted January 14, 2010 Report Share Posted January 14, 2010 I do understand how the medication works and the implications of fluid and electrolyte imbalances, etc. The thing is adding 2+2 togher and always coming to PEG is completely misleading. There are many medications including diuretics, osmotic laxatives, fleet and many many more that can alter electrolytes and fluids in the body.Quite frankly many more children and adults have suffered serious complications from the use of Fleet phosphate enemas than from miralax and it has a far worse track record for electrolyte problems than miralax. The answer is not to throw out all these meds. It is to more carefully monitor hydration and electrolyte levels in these patients. Particularly when they have pre existing conditions, eg renal failure and many others, that make them more vulnerable to these imbalances. If water and electrolytes are being lost due to any medication it is not rocket science that they then need to be replaced intravenously. Posting multiple links and selectively quoting in an attempt to 'blind them with science' is not really helping your cause. You have a bunch of people here that don't like miralax, but there's a bunch more who would rather not use it if they don't absolutely have to and would like information on alternatives and ways to get off whatever medication they are using, or at least move to one less strong. Constantly posting links that you infer say one thing, when in fact, taken in context don't say anything of the sort, and making assumptive leaps regarding causative associations, doesn't add credibility to your arguments. You are preaching to the converted for the most part but clearly there are others who would really prefer the facts, rather than selected 'facts' clouded by emotion. You assume they are on a 'different side', when the reality is that everyone is starting from the idea that they don't want to give their children medication at all. For some of us though, the end sometimes justifies the means at the time. The them and us approach that seems to characterise this group is one that is not doing it any favours if you really want serious discussion and scientific knowledge regarding miralax to be recognised, as opposed to emotive scaremongering. I know that you and others have had bad experiences with miralax, but there are probably thousands more whose children have had similar serious events with fleet. Their usual reaction is not to say 'ban Fleet for everyone'. It is to say that Fleet doesn't suit my child so we won't be using it again or to warn against using it in children that have specific other conditions. Rosemary New Zealand Mum to and 15, NID, Appendicostomy/Malone/ACE, Hypertonic sphincter, Sphincterotomy, Botox Feb 2008, Dyspraxia, Growth issues. July 2008 Started Interferential Therapy, October 2008….we have Poop! No more flushes since. Nov 2008, Scoliosis, pectus excavatum. > > > > Doesn't this quote put up red flags to anyone about the fact that this gentlemen is saying that if there was bad bacteria in the gut mcosal, that complications can happen? They know more than we're being told. Jack, this article is the one you shot down, saying they all had underlying conditions. But according to the rapid responses, this gentlemen had this to say......... .......... > >  > > I find it difficult to believe that intestinal secretion was the cause of the complications or deaths unless these patients had the unappreciated presence of gut mucosal ischaemia or bacterial infection such as C difficle. > > http://www.bmj. com/cgi/eletters /326/7385/ 382#29665 > >  > >  > > Therefore it's the bacteria in the gut that changes everything. Also, he says he finds it difficult to believe that intestinal secretion was the cause....... .....He doen't know for a fact. None of them know, this is why we were all involved in this " we don't know " study, so they could find out. Using our children!!!! > > Jeanie > > > Quote Link to comment Share on other sites More sharing options...
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