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My 13 month old daughter just came down with a cough last week after I was dianosed with a sinus infection she only would cough a couple of times at night when she was asleep or first thing in the morning and had a stuffy nose so I thought she just had a little cold but after a few days I became...

My 13 month old daughter just came down with a cough last week after I was dianosed with a sinus infection she only would cough a couple of times at night when she was asleep or first thing in the morning and had a stuffy nose so I thought she just had a little cold but after a few days I became...

My 13 month old daughter just came down with a cough last week after I was dianosed with a sinus infection she only would cough a couple of times at night when she was asleep or first thing in the morning and had a stuffy nose so I thought she just had a little cold but after a few days I became...

My 13 month old daughter just came down with a cough last week after I was dianosed with a sinus infection she only would cough a couple of times at night when she was asleep or first thing in the morning and had a stuffy nose so I thought she just had a little cold but after a few days I became...

My 13 month old daughter just came down with a cough last week after I was dianosed with a sinus infection she only would cough a couple of times at night when she was asleep or first thing in the morning and had a stuffy nose so I thought she just had a little cold but after a few days I became...

I read your post to Ambry and was amazed at how similar our situations are. I have a 13 month old daughter who was diagnosed with CF through the newborn screening program. She has also been non-symptomatic, and goes to the CF Clinic every 3 months for preventative measures. She is perfect for...

Hi, My daughter was diagnosed through the newborn screening program. She was sent for a sweat test, the first one came back as borderline as did the second one. They did the full genetic panel through Ambry and found DeltaF508, and another rare mutation of I1051F which according to Steve at...

Hi, My daughter was diagnosed through the newborn screening program. She was sent for a sweat test, the first one came back as borderline as did the second one. They did the full genetic panel through Ambry and found DeltaF508, and another rare mutation of I1051F which according to Steve at...

Hi, My daughter was diagnosed through the newborn screening program. She was sent for a sweat test, the first one came back as borderline as did the second one. They did the full genetic panel through Ambry and found DeltaF508, and another rare mutation of I1051F which according to Steve at...

Hi, My daughter was diagnosed through the newborn screening program. She was sent for a sweat test, the first one came back as borderline as did the second one. They did the full genetic panel through Ambry and found DeltaF508, and another rare mutation of I1051F which according to Steve at...

Hi, My daughter was diagnosed through the newborn screening program. She was sent for a sweat test, the first one came back as borderline as did the second one. They did the full genetic panel through Ambry and found DeltaF508, and another rare mutation of I1051F which according to Steve at...

Hi, My daughter was diagnosed through the newborn screening program. She was sent for a sweat test, the first one came back as borderline as did the second one. They did the full genetic panel through Ambry and found DeltaF508, and another rare mutation of I1051F which according to Steve at...

I am new to his site and have a question regarding my daughter. She is 7 months old and was diagnosed with CF through the newborn screening program. She had 2 sweat tests done in which both came back low borderline. They then decided to do the full genetics test through Ambry and it came back...

I am new to his site and have a question regarding my daughter. She is 7 months old and was diagnosed with CF through the newborn screening program. She had 2 sweat tests done in which both came back low borderline. They then decided to do the full genetics test through Ambry and it came back...

I am new to his site and have a question regarding my daughter. She is 7 months old and was diagnosed with CF through the newborn screening program. She had 2 sweat tests done in which both came back low borderline. They then decided to do the full genetics test through Ambry and it came back...