Recent content by kylesmommy

My son is five and has had a G-tube since he was two. He gets nighttime feedings from about 8 pm to 6 am. He has been fully potty trained during the daytime for quite some time, but at night has to wear Goodnights Underpants which (usually) absorb all or most of the urine. Since he is getting...

My son is five and has had a G-tube since he was two. He gets nighttime feedings from about 8 pm to 6 am. He has been fully potty trained during the daytime for quite some time, but at night has to wear Goodnights Underpants which (usually) absorb all or most of the urine. Since he is getting...

My son is five and has had a G-tube since he was two. He gets nighttime feedings from about 8 pm to 6 am. He has been fully potty trained during the daytime for quite some time, but at night has to wear Goodnights Underpants which (usually) absorb all or most of the urine. <br /> <br />Since...

What kind of G-tube is it? My son is 5 and started with a Bard Peg G-tube when he was 2. It had to be changed under anesthesia yearly. Two months ago it was switched to the Mic-Key brand G-tube, and we were told it has to be changed every three months. We don't run it as many hours however...

What kind of G-tube is it? My son is 5 and started with a Bard Peg G-tube when he was 2. It had to be changed under anesthesia yearly. Two months ago it was switched to the Mic-Key brand G-tube, and we were told it has to be changed every three months. We don't run it as many hours however...

What kind of G-tube is it? My son is 5 and started with a Bard Peg G-tube when he was 2. It had to be changed under anesthesia yearly. Two months ago it was switched to the Mic-Key brand G-tube, and we were told it has to be changed every three months. We don't run it as many hours however...

I recently found out about a foundation that assists with costs not covered by insurance. Check out www.patientaccessnetwork.org and click on Cystic Fibrosis, then there is an easy online application. Good Luck!

I recently found out about a foundation that assists with costs not covered by insurance. Check out www.patientaccessnetwork.org and click on Cystic Fibrosis, then there is an easy online application. Good Luck!

I recently found out about a foundation that assists with costs not covered by insurance. Check out www.patientaccessnetwork.org and click on Cystic Fibrosis, then there is an easy online application. Good Luck!

I recently found out about a foundation that assists with costs not covered by insurance. Check out www.patientaccessnetwork.org and click on Cystic Fibrosis, then there is an easy online application. Good Luck!

I recently found out about a foundation that assists with costs not covered by insurance. Check out www.patientaccessnetwork.org and click on Cystic Fibrosis, then there is an easy online application. Good Luck!

Deni, This is my first time on this forum. Your post caught my eye because my son has CF, and his mutations are also the dF508 and N1303K. My husband and I didn't know we were carriers, neither have family history, but apparently that is usually the case when CF is found. My son is now 2...

Deni, This is my first time on this forum. Your post caught my eye because my son has CF, and his mutations are also the dF508 and N1303K. My husband and I didn't know we were carriers, neither have family history, but apparently that is usually the case when CF is found. My son is now 2...

Deni, This is my first time on this forum. Your post caught my eye because my son has CF, and his mutations are also the dF508 and N1303K. My husband and I didn't know we were carriers, neither have family history, but apparently that is usually the case when CF is found. My son is now 2...

Deni, This is my first time on this forum. Your post caught my eye because my son has CF, and his mutations are also the dF508 and N1303K. My husband and I didn't know we were carriers, neither have family history, but apparently that is usually the case when CF is found. My son is now 2...