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I have never been to Hawaii so I have no first hand information...however, during our last visit to our CF Center in San Antonio, my 14 year old daughter told her doctor that she planned to go to college in Hawaii. The CF doctor told her that there are no CF Centers in Hawaii and that she just...

I have never been to Hawaii so I have no first hand information...however, during our last visit to our CF Center in San Antonio, my 14 year old daughter told her doctor that she planned to go to college in Hawaii. The CF doctor told her that there are no CF Centers in Hawaii and that she just...

I have never been to Hawaii so I have no first hand information...however, during our last visit to our CF Center in San Antonio, my 14 year old daughter told her doctor that she planned to go to college in Hawaii. The CF doctor told her that there are no CF Centers in Hawaii and that she just...

I have 3 children by birth and 2 by marriage. Of my biological children, 2 have CF.

I have 3 children by birth and 2 by marriage. Of my biological children, 2 have CF.

I have 3 children by birth and 2 by marriage. Of my biological children, 2 have CF.

I have 3 children by birth and 2 by marriage. Of my biological children, 2 have CF.

I have 3 children by birth and 2 by marriage. Of my biological children, 2 have CF.

Interesting. Thanks for posting the article. My daughters' doctor has told us that she is sure that my girls have a modifier of some type due to them both being DDF508 and having such mild lung disease but that there are tests or anything as of yet to verify that. It's a fascinating concept...

Interesting. Thanks for posting the article. My daughters' doctor has told us that she is sure that my girls have a modifier of some type due to them both being DDF508 and having such mild lung disease but that there are tests or anything as of yet to verify that. It's a fascinating concept...

Interesting. Thanks for posting the article. My daughters' doctor has told us that she is sure that my girls have a modifier of some type due to them both being DDF508 and having such mild lung disease but that there are tests or anything as of yet to verify that. It's a fascinating concept...

Interesting. Thanks for posting the article. My daughters' doctor has told us that she is sure that my girls have a modifier of some type due to them both being DDF508 and having such mild lung disease but that there are tests or anything as of yet to verify that. It's a fascinating concept...

Interesting. Thanks for posting the article. My daughters' doctor has told us that she is sure that my girls have a modifier of some type due to them both being DDF508 and having such mild lung disease but that there are tests or anything as of yet to verify that. It's a fascinating concept...

I have 5 kids... 3 boys without CF and 2 girls with CF. My CF'ers are 14 & 10. I remember before I ever had kids there was a woman at the church I went to who had a daughter who was severely brain damaged due to lack of oxygen before birth. She couldn't talk, walk, eat on her own...

I have 5 kids... 3 boys without CF and 2 girls with CF. My CF'ers are 14 & 10. I remember before I ever had kids there was a woman at the church I went to who had a daughter who was severely brain damaged due to lack of oxygen before birth. She couldn't talk, walk, eat on her own...

I have 5 kids... 3 boys without CF and 2 girls with CF. My CF'ers are 14 & 10. I remember before I ever had kids there was a woman at the church I went to who had a daughter who was severely brain damaged due to lack of oxygen before birth. She couldn't talk, walk, eat on her own...

I have 5 kids... 3 boys without CF and 2 girls with CF. My CF'ers are 14 & 10. I remember before I ever had kids there was a woman at the church I went to who had a daughter who was severely brain damaged due to lack of oxygen before birth. She couldn't talk, walk, eat on her own...

I have 5 kids... 3 boys without CF and 2 girls with CF. My CF'ers are 14 & 10. <br /> <br />I remember before I ever had kids there was a woman at the church I went to who had a daughter who was severely brain damaged due to lack of oxygen before birth. She couldn't talk, walk, eat on her...

It is a state run program and every state is different. I have lived in Kentucky, Minnesota and Texas and have had the program in all three states and they were all different. In Minnesota the program has an annual cap of $15,000 per child. They will not pay anything over that. (At least that...

It is a state run program and every state is different. I have lived in Kentucky, Minnesota and Texas and have had the program in all three states and they were all different. In Minnesota the program has an annual cap of $15,000 per child. They will not pay anything over that. (At least that...