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Thank you so much for this information, I wasn't aware of this. I have to ask do you know someone with these mutations or did you read this somewhere?

Thank you so much for this information, I wasn't aware of this. I have to ask do you know someone with these mutations or did you read this somewhere?

Hi i'd like to welcome you to this forum...reading this and seeing how you just found out 2 weeks ago takes me back 2 years ago and i handled everything. It's hard because everyone says something different but i just want to give you a piece of advice don't believe everything you read and take...

Hi i'd like to welcome you to this forum...reading this and seeing how you just found out 2 weeks ago takes me back 2 years ago and i handled everything. It's hard because everyone says something different but i just want to give you a piece of advice don't believe everything you read and take...

Hi i'd like to welcome you to this forum...reading this and seeing how you just found out 2 weeks ago takes me back 2 years ago and i handled everything. It's hard because everyone says something different but i just want to give you a piece of advice don't believe everything you read and take...

so my son was diagnosed with cf in 2009...his sweat tests were at a 7 the 2 times that they were done. they came back the same. we went ahead with the genetic testing and confirmed that he had delta f508 and a rare gene. My son will turn 2 in november. He has full pancreatic sufficiency if...

so my son was diagnosed with cf in 2009...his sweat tests were at a 7 the 2 times that they were done. they came back the same. we went ahead with the genetic testing and confirmed that he had delta f508 and a rare gene. My son will turn 2 in november. He has full pancreatic sufficiency if...

so my son was diagnosed with cf in 2009...his sweat tests were at a 7 the 2 times that they were done. they came back the same. we went ahead with the genetic testing and confirmed that he had delta f508 and a rare gene. My son will turn 2 in november. He has full pancreatic sufficiency if...

thanks for the information and i think i wrote it wrong the doctors told me the mutation here in the u.s. is rare and he's the first patient they've seen with that particular gene. I'm hopeful and thankful that he's healthy but i'm a nurse and i do alot a research and i try to keep myself...

thanks for the information and i think i wrote it wrong the doctors told me the mutation here in the u.s. is rare and he's the first patient they've seen with that particular gene. I'm hopeful and thankful that he's healthy but i'm a nurse and i do alot a research and i try to keep myself...

thanks for the information and i think i wrote it wrong the doctors told me the mutation here in the u.s. is rare and he's the first patient they've seen with that particular gene. I'm hopeful and thankful that he's healthy but i'm a nurse and i do alot a research and i try to keep myself...

Hi so my son was diagnosed in 2010 after the ambry genetics test was done, so it turns out that he has the most common gene which is the delta f508 but the second one which is c.4375-20A>G. is really rare as far as the doctors told me about 2% of the cf population has this gene. I am taking my...

Hi so my son was diagnosed in 2010 after the ambry genetics test was done, so it turns out that he has the most common gene which is the delta f508 but the second one which is c.4375-20A>G. is really rare as far as the doctors told me about 2% of the cf population has this gene. I am taking my...

<BR>Hi so my son was diagnosed in 2010 after the ambry genetics test was done, so it turns out that he has the most common gene which is the delta f508 but the second one which is c.4375-20A>G. is really rare as far as the doctors told me about 2% of the cf population has this gene. I am taking...