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My daughter wasn't diagnosed until she was 14 years old, so what I have to say is not the same as having a very young child with PA and Staph - but wanted to let you know that yes, it does happen to others at 6 months and even younger, and yes some people do get rid of both PA and staph when...
My daughter wasn't diagnosed until she was 14 years old, so what I have to say is not the same as having a very young child with PA and Staph - but wanted to let you know that yes, it does happen to others at 6 months and even younger, and yes some people do get rid of both PA and staph when...
My daughter wasn't diagnosed until she was 14 years old, so what I have to say is not the same as having a very young child with PA and Staph - but wanted to let you know that yes, it does happen to others at 6 months and even younger, and yes some people do get rid of both PA and staph when...
My daughter wasn't diagnosed until she was 14 years old, so what I have to say is not the same as having a very young child with PA and Staph - but wanted to let you know that yes, it does happen to others at 6 months and even younger, and yes some people do get rid of both PA and staph when...
My daughter wasn't diagnosed until she was 14 years old, so what I have to say is not the same as having a very young child with PA and Staph - but wanted to let you know that yes, it does happen to others at 6 months and even younger, and yes some people do get rid of both PA and staph when...
<b>trinitycf</b>
Maria,
Did you get genetic testing on your girls? Do you know what their mutations are - just curious, since I have read that it is very rare in African Americans -- just curious what genes they have.
Glad to hear you did eventually get the correct diagnosis - I know it is...
<b>trinitycf</b>
Maria,
Did you get genetic testing on your girls? Do you know what their mutations are - just curious, since I have read that it is very rare in African Americans -- just curious what genes they have.
Glad to hear you did eventually get the correct diagnosis - I know it is...
<b>trinitycf</b>
Maria,
Did you get genetic testing on your girls? Do you know what their mutations are - just curious, since I have read that it is very rare in African Americans -- just curious what genes they have.
Glad to hear you did eventually get the correct diagnosis - I know it is...
<b>trinitycf</b>
Maria,
Did you get genetic testing on your girls? Do you know what their mutations are - just curious, since I have read that it is very rare in African Americans -- just curious what genes they have.
Glad to hear you did eventually get the correct diagnosis - I know it is...
<b>trinitycf</b>
Maria,
Did you get genetic testing on your girls? Do you know what their mutations are - just curious, since I have read that it is very rare in African Americans -- just curious what genes they have.
Glad to hear you did eventually get the correct diagnosis - I know it is...
I am confused about the "complex carrier and the "benign variant" part (just never heard the terms before -- of course I know what the words mean, just not used in relation to a CF diagnosis) .... but I wanted to let you know what has happened with us so you would have it in your brain, in case...
I am confused about the "complex carrier and the "benign variant" part (just never heard the terms before -- of course I know what the words mean, just not used in relation to a CF diagnosis) .... but I wanted to let you know what has happened with us so you would have it in your brain, in case...
I am confused about the "complex carrier and the "benign variant" part (just never heard the terms before -- of course I know what the words mean, just not used in relation to a CF diagnosis) .... but I wanted to let you know what has happened with us so you would have it in your brain, in case...
I am confused about the "complex carrier and the "benign variant" part (just never heard the terms before -- of course I know what the words mean, just not used in relation to a CF diagnosis) .... but I wanted to let you know what has happened with us so you would have it in your brain, in case...
I am confused about the "complex carrier and the "benign variant" part (just never heard the terms before -- of course I know what the words mean, just not used in relation to a CF diagnosis) .... but I wanted to let you know what has happened with us so you would have it in your brain, in case...
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