Married couple carriers for df508

flatfordl

New member
My husband and I are both df508 carriers as well. We have two children one with Cf and one without. Our daughter is doing really well. Besides all the meds and daily treatments you would never know she has cf because she is so healthy.

Take care and good luck. This forum is a great place to get answers.
 

flatfordl

New member
My husband and I are both df508 carriers as well. We have two children one with Cf and one without. Our daughter is doing really well. Besides all the meds and daily treatments you would never know she has cf because she is so healthy.

Take care and good luck. This forum is a great place to get answers.
 

flatfordl

New member
My husband and I are both df508 carriers as well. We have two children one with Cf and one without. Our daughter is doing really well. Besides all the meds and daily treatments you would never know she has cf because she is so healthy.

Take care and good luck. This forum is a great place to get answers.
 

flatfordl

New member
My husband and I are both df508 carriers as well. We have two children one with Cf and one without. Our daughter is doing really well. Besides all the meds and daily treatments you would never know she has cf because she is so healthy.

Take care and good luck. This forum is a great place to get answers.
 

flatfordl

New member
My husband and I are both df508 carriers as well. We have two children one with Cf and one without. Our daughter is doing really well. Besides all the meds and daily treatments you would never know she has cf because she is so healthy.
<br />
<br />Take care and good luck. This forum is a great place to get answers.
<br />
<br />
 

kate620

New member
Being a carrier wouldn't affect his ability to have kids and don't be shocked nobody in your family has it. You wouldn't have it unless 2 people got together that carried the gene and then it's a 1 in 4 chance the kid will get it. If I had known her dad and I were both carriers and she would end up with this disease, I probably would not have planned a pregnancy but I'm glad I did not know because she is the best thing that has ever happed to me.

<img src="http://i426.photobucket.com/albums/pp350/katie620_01/223.jpg">
 

kate620

New member
Being a carrier wouldn't affect his ability to have kids and don't be shocked nobody in your family has it. You wouldn't have it unless 2 people got together that carried the gene and then it's a 1 in 4 chance the kid will get it. If I had known her dad and I were both carriers and she would end up with this disease, I probably would not have planned a pregnancy but I'm glad I did not know because she is the best thing that has ever happed to me.

<img src="http://i426.photobucket.com/albums/pp350/katie620_01/223.jpg">
 

kate620

New member
Being a carrier wouldn't affect his ability to have kids and don't be shocked nobody in your family has it. You wouldn't have it unless 2 people got together that carried the gene and then it's a 1 in 4 chance the kid will get it. If I had known her dad and I were both carriers and she would end up with this disease, I probably would not have planned a pregnancy but I'm glad I did not know because she is the best thing that has ever happed to me.

<img src="http://i426.photobucket.com/albums/pp350/katie620_01/223.jpg">
 

kate620

New member
Being a carrier wouldn't affect his ability to have kids and don't be shocked nobody in your family has it. You wouldn't have it unless 2 people got together that carried the gene and then it's a 1 in 4 chance the kid will get it. If I had known her dad and I were both carriers and she would end up with this disease, I probably would not have planned a pregnancy but I'm glad I did not know because she is the best thing that has ever happed to me.

<img src="http://i426.photobucket.com/albums/pp350/katie620_01/223.jpg">
 

kate620

New member
Being a carrier wouldn't affect his ability to have kids and don't be shocked nobody in your family has it. You wouldn't have it unless 2 people got together that carried the gene and then it's a 1 in 4 chance the kid will get it. If I had known her dad and I were both carriers and she would end up with this disease, I probably would not have planned a pregnancy but I'm glad I did not know because she is the best thing that has ever happed to me.
<br />
<br /><img src="http://i426.photobucket.com/albums/pp350/katie620_01/223.jpg">
 

grammakaky

New member
my daughter and son-in-law found out they were carriers while she was pregant, and it also was never in our family. They have a beautiful little girl; who just happens to have cf, and she's the love of our lives and the best little girl ever.
 

grammakaky

New member
my daughter and son-in-law found out they were carriers while she was pregant, and it also was never in our family. They have a beautiful little girl; who just happens to have cf, and she's the love of our lives and the best little girl ever.
 

grammakaky

New member
my daughter and son-in-law found out they were carriers while she was pregant, and it also was never in our family. They have a beautiful little girl; who just happens to have cf, and she's the love of our lives and the best little girl ever.
 

grammakaky

New member
my daughter and son-in-law found out they were carriers while she was pregant, and it also was never in our family. They have a beautiful little girl; who just happens to have cf, and she's the love of our lives and the best little girl ever.
 

grammakaky

New member
my daughter and son-in-law found out they were carriers while she was pregant, and it also was never in our family. They have a beautiful little girl; who just happens to have cf, and she's the love of our lives and the best little girl ever.
 

grassisgreener

New member
www.cff.org is the website for the Cystic Fibrosis Foundation. This has alot of good information. I am sorry they are carriers. My husband and I didn't know that we are both carriers until after our daughter was diagnosed when she was 12 months old. She is now 5.5 years old, is doing really well and is a true blessing to us.

As for stats it is something like 1 in 25 people is a carrier, 1 in 400 marriages are 2 carriers and then when two carriers have children there is a 1 in 4 chance that each child could have CF. I know of several families that have 2 or 3 kids that all have CF. I also know of several families that have 4+ kids and only one of them has CF. One lady that lives near me was the last born of 8 kids and she is the only one that has CF.
 

grassisgreener

New member
www.cff.org is the website for the Cystic Fibrosis Foundation. This has alot of good information. I am sorry they are carriers. My husband and I didn't know that we are both carriers until after our daughter was diagnosed when she was 12 months old. She is now 5.5 years old, is doing really well and is a true blessing to us.

As for stats it is something like 1 in 25 people is a carrier, 1 in 400 marriages are 2 carriers and then when two carriers have children there is a 1 in 4 chance that each child could have CF. I know of several families that have 2 or 3 kids that all have CF. I also know of several families that have 4+ kids and only one of them has CF. One lady that lives near me was the last born of 8 kids and she is the only one that has CF.
 

grassisgreener

New member
www.cff.org is the website for the Cystic Fibrosis Foundation. This has alot of good information. I am sorry they are carriers. My husband and I didn't know that we are both carriers until after our daughter was diagnosed when she was 12 months old. She is now 5.5 years old, is doing really well and is a true blessing to us.

As for stats it is something like 1 in 25 people is a carrier, 1 in 400 marriages are 2 carriers and then when two carriers have children there is a 1 in 4 chance that each child could have CF. I know of several families that have 2 or 3 kids that all have CF. I also know of several families that have 4+ kids and only one of them has CF. One lady that lives near me was the last born of 8 kids and she is the only one that has CF.
 

grassisgreener

New member
www.cff.org is the website for the Cystic Fibrosis Foundation. This has alot of good information. I am sorry they are carriers. My husband and I didn't know that we are both carriers until after our daughter was diagnosed when she was 12 months old. She is now 5.5 years old, is doing really well and is a true blessing to us.

As for stats it is something like 1 in 25 people is a carrier, 1 in 400 marriages are 2 carriers and then when two carriers have children there is a 1 in 4 chance that each child could have CF. I know of several families that have 2 or 3 kids that all have CF. I also know of several families that have 4+ kids and only one of them has CF. One lady that lives near me was the last born of 8 kids and she is the only one that has CF.
 

grassisgreener

New member
www.cff.org is the website for the Cystic Fibrosis Foundation. This has alot of good information. I am sorry they are carriers. My husband and I didn't know that we are both carriers until after our daughter was diagnosed when she was 12 months old. She is now 5.5 years old, is doing really well and is a true blessing to us.
<br />
<br />As for stats it is something like 1 in 25 people is a carrier, 1 in 400 marriages are 2 carriers and then when two carriers have children there is a 1 in 4 chance that each child could have CF. I know of several families that have 2 or 3 kids that all have CF. I also know of several families that have 4+ kids and only one of them has CF. One lady that lives near me was the last born of 8 kids and she is the only one that has CF.
 
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