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Thank you for the Reply, Emily. I hope you are doing well. It is nice to see all of the adults participating in this board. I lurk sometimes just to see what issues affect everyone.

Thank for your response, Moxie. You are correct about PTC124. I have been reading alot about it. We have discussed it with our Genetics person at the U of M Clinic and she thinks it is very promising. I hope it is the 'answer' for my little girl. :-)

Thank for your response, Moxie. You are correct about PTC124. I have been reading alot about it. We have discussed it with our Genetics person at the U of M Clinic and she thinks it is very promising. I hope it is the 'answer' for my little girl. :-)

Thank for your response, Moxie. You are correct about PTC124. I have been reading alot about it. We have discussed it with our Genetics person at the U of M Clinic and she thinks it is very promising. I hope it is the 'answer' for my little girl. :-)

Thank for your response, Moxie. You are correct about PTC124. I have been reading alot about it. We have discussed it with our Genetics person at the U of M Clinic and she thinks it is very promising. I hope it is the 'answer' for my little girl. :-)

Thank for your response, Moxie. You are correct about PTC124. I have been reading alot about it. We have discussed it with our Genetics person at the U of M Clinic and she thinks it is very promising. I hope it is the 'answer' for my little girl. :-)

My daughter is a newborn (about 10 weeks old). I want her to grow up happy, healthy, and knowing she is more than her illness. Do you have any advice for a parent with a child who has CF? What did your parents do right? What did your parents do wrong? What would be most important to you...

My daughter is a newborn (about 10 weeks old). I want her to grow up happy, healthy, and knowing she is more than her illness. Do you have any advice for a parent with a child who has CF? What did your parents do right? What did your parents do wrong? What would be most important to you...

My daughter is a newborn (about 10 weeks old). I want her to grow up happy, healthy, and knowing she is more than her illness. Do you have any advice for a parent with a child who has CF? What did your parents do right? What did your parents do wrong? What would be most important to you...

My daughter is a newborn (about 10 weeks old). I want her to grow up happy, healthy, and knowing she is more than her illness. Do you have any advice for a parent with a child who has CF? What did your parents do right? What did your parents do wrong? What would be most important to you...

My daughter is a newborn (about 10 weeks old). I want her to grow up happy, healthy, and knowing she is more than her illness. Do you have any advice for a parent with a child who has CF? What did your parents do right? What did your parents do wrong? What would be most important to you...

These are the mutation my daughter has. I know that everyone is different and that 2 people with the same mutations will not have the same disease. With all that being said... I am still curious if there are any adults on here that have the same mutations. If yes, how are you doing?

These are the mutation my daughter has. I know that everyone is different and that 2 people with the same mutations will not have the same disease. With all that being said... I am still curious if there are any adults on here that have the same mutations. If yes, how are you doing?

These are the mutation my daughter has. I know that everyone is different and that 2 people with the same mutations will not have the same disease. With all that being said... I am still curious if there are any adults on here that have the same mutations. If yes, how are you doing?

These are the mutation my daughter has. I know that everyone is different and that 2 people with the same mutations will not have the same disease. With all that being said... I am still curious if there are any adults on here that have the same mutations. If yes, how are you doing?

These are the mutation my daughter has. I know that everyone is different and that 2 people with the same mutations will not have the same disease. With all that being said... I am still curious if there are any adults on here that have the same mutations. If yes, how are you doing?

The best place to start for information is <a target=_blank class=ftalternatingbarlinklarge href="http://www.cff.org/ ">http://www.cff.org/ </a> <b>What Is Cystic Fibrosis?</b> Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children...

The best place to start for information is <a target=_blank class=ftalternatingbarlinklarge href="http://www.cff.org/ ">http://www.cff.org/ </a> <b>What Is Cystic Fibrosis?</b> Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children...

The best place to start for information is <a target=_blank class=ftalternatingbarlinklarge href="http://www.cff.org/ ">http://www.cff.org/ </a> <b>What Is Cystic Fibrosis?</b> Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children...

The best place to start for information is <a target=_blank class=ftalternatingbarlinklarge href="http://www.cff.org/ ">http://www.cff.org/ </a> <b>What Is Cystic Fibrosis?</b> Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children...