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Thanks dyza! That definitely gives me a starting point! <img src="i/expressions/face-icon-small-smile.gif" border="0">

Thanks dyza! That definitely gives me a starting point! <img src="i/expressions/face-icon-small-smile.gif" border="0">

I have tried the sickkids website several times and still cannot find my son's second mutation. Does anyone else have any information or sources that could tell me what mutation class it belongs in? My son has a clinic appointment in 2 weeks, so if I can't find anything out by then I'll see if...

I have tried the sickkids website several times and still cannot find my son's second mutation. Does anyone else have any information or sources that could tell me what mutation class it belongs in? My son has a clinic appointment in 2 weeks, so if I can't find anything out by then I'll see if...

I guess I made him sound worse than I should have. It's just when I try to ask mutation specific questions, he always tells me not to put too much emphasis on them, because they don't hold a direct relation to the severity of the disease. I realize this, but my main focus is just to understand...

I guess I made him sound worse than I should have. It's just when I try to ask mutation specific questions, he always tells me not to put too much emphasis on them, because they don't hold a direct relation to the severity of the disease. I realize this, but my main focus is just to understand...

I've been reading a lot lately about the different CF mutation classes and what they mean. My question is, where can I find out exactly what class my son's 2nd, more rare mutation is in? Our clinic doesn't have a geneticist, and his doctor doesn't give me direct answers.

I've been reading a lot lately about the different CF mutation classes and what they mean. My question is, where can I find out exactly what class my son's 2nd, more rare mutation is in? Our clinic doesn't have a geneticist, and his doctor doesn't give me direct answers.

Wow, I just read this and it's awesome news! Is it possible to use the code now in Kentucky? We actually attend the clinic in Lexington. I'd love some more information on this so that I can share it with my friends and family. Praying for a great outcome with this! PS: just joined your...

Wow, I just read this and it's awesome news! Is it possible to use the code now in Kentucky? We actually attend the clinic in Lexington. I'd love some more information on this so that I can share it with my friends and family. Praying for a great outcome with this! PS: just joined your...

Wow, I just read this and it's awesome news! Is it possible to use the code now in Kentucky? We actually attend the clinic in Lexington. I'd love some more information on this so that I can share it with my friends and family. Praying for a great outcome with this! <br /> <br />PS: just...

My son does have the same exact mutations and so far he has been very healthy. He will be 17 months old next week, and to this date hasn't had the first problem with mucus. He also tested as being pancreatic sufficient. He does have chronic constipation and has to have Miralax twice daily...

My son does have the same exact mutations and so far he has been very healthy. He will be 17 months old next week, and to this date hasn't had the first problem with mucus. He also tested as being pancreatic sufficient. He does have chronic constipation and has to have Miralax twice daily...

My son does have the same exact mutations and so far he has been very healthy. He will be 17 months old next week, and to this date hasn't had the first problem with mucus. He also tested as being pancreatic sufficient. He does have chronic constipation and has to have Miralax twice daily...

I can understand how scared you all are. I was in the same boat about 2 years ago. I was told while I was pregnant that I was a carrier for CF. Like you, I knew of no one on either side of the family with CF, and to be honest, didn't know anything about the disease. My OB arranged for my...

I can understand how scared you all are. I was in the same boat about 2 years ago. I was told while I was pregnant that I was a carrier for CF. Like you, I knew of no one on either side of the family with CF, and to be honest, didn't know anything about the disease. My OB arranged for my...

I can understand how scared you all are. I was in the same boat about 2 years ago. I was told while I was pregnant that I was a carrier for CF. Like you, I knew of no one on either side of the family with CF, and to be honest, didn't know anything about the disease. My OB arranged for my...

Nancy, I was diagnosed with gestational diabetes at 24 weeks. I have high blood pressure and also had to be monitored closely. I live in a very rural area and my OB didn't feel like he had all the technology to monitor the baby and my blood pressure issues, so he refered me to another doctor...

Nancy, I was diagnosed with gestational diabetes at 24 weeks. I have high blood pressure and also had to be monitored closely. I live in a very rural area and my OB didn't feel like he had all the technology to monitor the baby and my blood pressure issues, so he refered me to another doctor...

Nancy, I was diagnosed with gestational diabetes at 24 weeks. I have high blood pressure and also had to be monitored closely. I live in a very rural area and my OB didn't feel like he had all the technology to monitor the baby and my blood pressure issues, so he refered me to another doctor...