Guest guest Posted March 17, 2003 Report Share Posted March 17, 2003 > wow-that is a lot to deal with at one time. My son is 2, it was only a short 31/2 weeks ago we found out about his CF. But in that short time his bowel movements have changed alot. Are they sure she is on the right enzymes and that she is getting enough of them? I only ask because my son drinks a lot of milk too and doesn't seem to have a problem with his bm's anymore. I would talk to the CF dr. and maybe try to up her enzyme intake a little to see if that helps. I will keep you in my heart and prayer for your daughter and husband. I will give you some good advice that I got when I first joined this list. Go on automatic pilot for a little while and it will all fall in place. At first I couldn't do this but it gets easier. The second best advice on I got was this: stop, breath, scream, cry.......now you are ready to take in all that you will need to. (that's not exactly how it was said, but that was the jist of it). We are always glad ( & sad)to welcome new members. This group will have alot of advice and it is generally good and useful. > > Date: 2003/03/16 Sun PM 11:36:14 EST > To: cfparents > Subject: Hi im new & little strest > > Christal mom of Tristan 6ncf, Zack 2wcf & asthma, Ki'a 4mthsncf Quote Link to comment Share on other sites More sharing options...
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