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<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Bridge76</b></i> <br /> <br />That's interesting - what made you try that? How do you get it down a 2 year old?</end quote> <br /> <br />I found it here (someone else had good results so i saw no harm in trying): <br /> <br /><a...

I found that freshly squeezed lemon juice helped my daughter. She is only two and is not producing that much, but nowdays the RT that sees her every day is having a hard time getting anything much at all.

I found that freshly squeezed lemon juice helped my daughter. She is only two and is not producing that much, but nowdays the RT that sees her every day is having a hard time getting anything much at all.

I found that freshly squeezed lemon juice helped my daughter. She is only two and is not producing that much, but nowdays the RT that sees her every day is having a hard time getting anything much at all.

I agree with Caroline. Some of the choices i made for my dd might not be very popular and are definitely not the mainstream on the forum, but as an adult with a chronic desease myself, i really know way too well what it is like to be sick/in the hospital all the time. That is why i feel that...

I agree with Caroline. Some of the choices i made for my dd might not be very popular and are definitely not the mainstream on the forum, but as an adult with a chronic desease myself, i really know way too well what it is like to be sick/in the hospital all the time. That is why i feel that...

I agree with Caroline. Some of the choices i made for my dd might not be very popular and are definitely not the mainstream on the forum, but as an adult with a chronic desease myself, i really know way too well what it is like to be sick/in the hospital all the time. That is why i feel that...

we have sputum culture done by RT at every visit. unless the child has very little sputum they try to get a sample since it seems to be more reliable, even though as others mentioned bugs can still be missed.

we have sputum culture done by RT at every visit. unless the child has very little sputum they try to get a sample since it seems to be more reliable, even though as others mentioned bugs can still be missed.

we have sputum culture done by RT at every visit. unless the child has very little sputum they try to get a sample since it seems to be more reliable, even though as others mentioned bugs can still be missed.

I agree with kitomd21 thqt certain activities cqrry higher risks and while my dd is little, i would rather steer her towards activities where she is less likely to be exposed to certain germs. I really feel that she would thank me one day for preserving her health. Of course, as with...

I agree with kitomd21 thqt certain activities cqrry higher risks and while my dd is little, i would rather steer her towards activities where she is less likely to be exposed to certain germs. I really feel that she would thank me one day for preserving her health. Of course, as with...

I agree with kitomd21 thqt certain activities cqrry higher risks and while my dd is little, i would rather steer her towards activities where she is less likely to be exposed to certain germs. <br /> <br />I really feel that she would thank me one day for preserving her health. Of course, as...

we have clinic visits every 3 months but i get my dd cultured about every month. we started it on our doctor's recommendation when she first cultured PA, but now i read that every 3 months is the MINIMUM (based on European CF Society concensus), ideally it should be done every month (regardless...

we have clinic visits every 3 months but i get my dd cultured about every month. we started it on our doctor's recommendation when she first cultured PA, but now i read that every 3 months is the MINIMUM (based on European CF Society concensus), ideally it should be done every month (regardless...

we have clinic visits every 3 months but i get my dd cultured about every month. we started it on our doctor's recommendation when she first cultured PA, but now i read that every 3 months is the MINIMUM (based on European CF Society concensus), ideally it should be done every month (regardless...

<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>kitomd21</b></i> Hmm...we give Ellie sea salt, but didn't know there was a potential benefit to the magnesium component. I did give her DHA for a few months, but discontinued as she doesn't care for the taste. I discussed DHA...

<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>kitomd21</b></i> Hmm...we give Ellie sea salt, but didn't know there was a potential benefit to the magnesium component. I did give her DHA for a few months, but discontinued as she doesn't care for the taste. I discussed DHA...

<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>kitomd21</b></i> <br /> <br />Hmm...we give Ellie sea salt, but didn't know there was a potential benefit to the magnesium component. <br /> <br /> <br /> <br />I did give her DHA for a few months, but discontinued as she doesn't...

My dd had infant pfts done when she was 1 yr old. Our hospital does them routinely as long as they can make them fall asleep (which was not the case for my dd this year). She did not have any strange reaction to it that i can remember.