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my dd cultured PA when she was 15 mo. She did 3 courses of Tobi (with 2 weeks of Cipro in the beginning) even though it was gone after the first one (she had a very small colony of PA). While we were doing Tobi I was told by the doctor to do culture every month. <br /> <br />Even though we have...

<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>edan</b></i> Hi Jmom, I am sorry you are having to go through this. But once you get the right answers you will be able to proactively help your child. I am certainly glad we found out. We just found out my daughter has CF...

<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>edan</b></i> Hi Jmom, I am sorry you are having to go through this. But once you get the right answers you will be able to proactively help your child. I am certainly glad we found out. We just found out my daughter has CF...

<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>edan</b></i> <br /> <br />Hi Jmom, <br /> <br /> <br /> <br />I am sorry you are having to go through this. But once you get the right answers you will be able to proactively help your child. I am certainly glad we found out. <br...

Hi, I cannot remember where I read it but it said that CF patient's pancreas is affected even when he is PS, that is why their elastase would be lower than 500. Having said that, I think there is a member here whose number is above 500 and she still has CF, so I would not base the CF diagnosis...

Hi, I cannot remember where I read it but it said that CF patient's pancreas is affected even when he is PS, that is why their elastase would be lower than 500. Having said that, I think there is a member here whose number is above 500 and she still has CF, so I would not base the CF diagnosis...

Hi, <br />I cannot remember where I read it but it said that CF patient's pancreas is affected even when he is PS, that is why their elastase would be lower than 500. <br /> <br />Having said that, I think there is a member here whose number is above 500 and she still has CF, so I would not base...

My dd is 2.5 y/o and had this problem until recently. She was put on antiacid and it did get better although she still gags occasionally. I also give her mostly mashed food, she would eat grown up food but not enough in terms of quantity, she just gets sick of chewing I guess. One thing I...

My dd is 2.5 y/o and had this problem until recently. She was put on antiacid and it did get better although she still gags occasionally. I also give her mostly mashed food, she would eat grown up food but not enough in terms of quantity, she just gets sick of chewing I guess. One thing I...

My dd is 2.5 y/o and had this problem until recently. She was put on antiacid and it did get better although she still gags occasionally. <br /> <br />I also give her mostly mashed food, she would eat grown up food but not enough in terms of quantity, she just gets sick of chewing I guess. <br...

my dd is also PS but had constipation issues from the very start. i give her papaye puree daily, it really helps. So far we managed without Miralax

my dd is also PS but had constipation issues from the very start. i give her papaye puree daily, it really helps. So far we managed without Miralax

my dd is also PS but had constipation issues from the very start. i give her papaye puree daily, it really helps. So far we managed without Miralax

you are right about symptoms being different. My dd was diagnosed with neo natal screening and she had no cough and no other symptoms, just kind of liquid stools (from time to time) and was crying a lot after meals. the Ped wrote it off as colics. I am so grateful that we have neonatal...

you are right about symptoms being different. My dd was diagnosed with neo natal screening and she had no cough and no other symptoms, just kind of liquid stools (from time to time) and was crying a lot after meals. the Ped wrote it off as colics. I am so grateful that we have neonatal...

you are right about symptoms being different. My dd was diagnosed with neo natal screening and she had no cough and no other symptoms, just kind of liquid stools (from time to time) and was crying a lot after meals. the Ped wrote it off as colics. I am so grateful that we have neonatal...

gaining weight for young kidsI ami <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Frida</b></i> Were in Europe are you ? I'm in Iceland and been thinking about trying coconut oil. Were to you buy it online ? Frida</end quote></div> i am in France, i buy it at vitashop.be, it...

gaining weight for young kidsI ami <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Frida</b></i> Were in Europe are you ? I'm in Iceland and been thinking about trying coconut oil. Were to you buy it online ? Frida</end quote> i am in France, i buy it at vitashop.be, it must...

gaining weight for young kidsI ami <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Frida</b></i> <br /> <br />Were in Europe are you ? I'm in Iceland and been thinking about trying coconut oil. Were to you buy it online ? <br /> <br /> <br /> <br />Frida</end quote> <br /> <br />i...

<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>SadiesMom</b></i> does it change the consistency? I've been thinking of adding oil to her meals, but I'm afraid it'll change the consistency. Like for example, in yogurt?? Are there things you can't mix it with?</end quote></div>...