husband with cf. Starting IVF

[rvm1212]

Thank you for the answers. <img src="i/expressions/face-icon-small-smile.gif" border="0">

Julie, I would love to know about other people going throw ivf. My e-mail is rvm1212@yahoo.es

Mon2lillian, my boyfriend was not only diagnosed because of infertility, although it helped. He had been preaviously diagnosed with mild bronchiectasies at 33 (normal xray, only seen in ct), after going to many, many, many doctors, due to bronchitis in winter that would last more than normal, and after been said many times that there were just viruses and that it was normal to cough during winter. First sweat test was normal, so they said not cf. After asking many times for the genetic test they just decided to do it after we found out he was azoospermic. Before they said "it was impossible he would have cf at his age, with normal lung funtion and without being colonized by pseudomona".

Bonniebaby, I don´t know if cvs will help too much since we already know the baby is going to carry one of his mutations and I don´t have any mutations, or at least any of the known ones, since I have a negative full ambry test. I don´t live in USA, but I have checked, and they do the cf newborn screening here in spain.

 

[rvm1212]

Thank you for the answers. <img src="i/expressions/face-icon-small-smile.gif" border="0">

Julie, I would love to know about other people going throw ivf. My e-mail is rvm1212@yahoo.es

Mon2lillian, my boyfriend was not only diagnosed because of infertility, although it helped. He had been preaviously diagnosed with mild bronchiectasies at 33 (normal xray, only seen in ct), after going to many, many, many doctors, due to bronchitis in winter that would last more than normal, and after been said many times that there were just viruses and that it was normal to cough during winter. First sweat test was normal, so they said not cf. After asking many times for the genetic test they just decided to do it after we found out he was azoospermic. Before they said "it was impossible he would have cf at his age, with normal lung funtion and without being colonized by pseudomona".

Bonniebaby, I don´t know if cvs will help too much since we already know the baby is going to carry one of his mutations and I don´t have any mutations, or at least any of the known ones, since I have a negative full ambry test. I don´t live in USA, but I have checked, and they do the cf newborn screening here in spain.

 

[rvm1212]

Thank you for the answers. <img src="i/expressions/face-icon-small-smile.gif" border="0">

Julie, I would love to know about other people going throw ivf. My e-mail is rvm1212@yahoo.es

Mon2lillian, my boyfriend was not only diagnosed because of infertility, although it helped. He had been preaviously diagnosed with mild bronchiectasies at 33 (normal xray, only seen in ct), after going to many, many, many doctors, due to bronchitis in winter that would last more than normal, and after been said many times that there were just viruses and that it was normal to cough during winter. First sweat test was normal, so they said not cf. After asking many times for the genetic test they just decided to do it after we found out he was azoospermic. Before they said "it was impossible he would have cf at his age, with normal lung funtion and without being colonized by pseudomona".

Bonniebaby, I don´t know if cvs will help too much since we already know the baby is going to carry one of his mutations and I don´t have any mutations, or at least any of the known ones, since I have a negative full ambry test. I don´t live in USA, but I have checked, and they do the cf newborn screening here in spain.

 

[rvm1212]

Thank you for the answers. <img src="i/expressions/face-icon-small-smile.gif" border="0">

Julie, I would love to know about other people going throw ivf. My e-mail is rvm1212@yahoo.es

Mon2lillian, my boyfriend was not only diagnosed because of infertility, although it helped. He had been preaviously diagnosed with mild bronchiectasies at 33 (normal xray, only seen in ct), after going to many, many, many doctors, due to bronchitis in winter that would last more than normal, and after been said many times that there were just viruses and that it was normal to cough during winter. First sweat test was normal, so they said not cf. After asking many times for the genetic test they just decided to do it after we found out he was azoospermic. Before they said "it was impossible he would have cf at his age, with normal lung funtion and without being colonized by pseudomona".

Bonniebaby, I don´t know if cvs will help too much since we already know the baby is going to carry one of his mutations and I don´t have any mutations, or at least any of the known ones, since I have a negative full ambry test. I don´t live in USA, but I have checked, and they do the cf newborn screening here in spain.

 

[rvm1212]

Thank you for the answers. <img src="i/expressions/face-icon-small-smile.gif" border="0">
<br />
<br />Julie, I would love to know about other people going throw ivf. My e-mail is rvm1212@yahoo.es
<br />
<br />Mon2lillian, my boyfriend was not only diagnosed because of infertility, although it helped. He had been preaviously diagnosed with mild bronchiectasies at 33 (normal xray, only seen in ct), after going to many, many, many doctors, due to bronchitis in winter that would last more than normal, and after been said many times that there were just viruses and that it was normal to cough during winter. First sweat test was normal, so they said not cf. After asking many times for the genetic test they just decided to do it after we found out he was azoospermic. Before they said "it was impossible he would have cf at his age, with normal lung funtion and without being colonized by pseudomona".
<br />
<br />Bonniebaby, I don´t know if cvs will help too much since we already know the baby is going to carry one of his mutations and I don´t have any mutations, or at least any of the known ones, since I have a negative full ambry test. I don´t live in USA, but I have checked, and they do the cf newborn screening here in spain.

 

[LouLou]

I thought I better commment in case you read somewhere on here about my son testing positive after negative carrier testing in father. He was only screened for 89 mutations NOT THE FULL +1500 AMBRY TESTS FOR.

I have cf. Dh carries S1235R. My son does not test positive for cf through either sweat or IRT birth levels...only genetically. He is also still considered symptomless albeit we do preventative lung clearance care and treat any cough lasting over 4 days with antibiotics. He also is pancreatic sufficient yet give him ABDEK vitamins with a "it can't hurt" philosophy.

I think you need not worry about cf. At this point the chances of one of the many other than cf issues a baby can have are greater I'd say. Not to add to your worry

Also if english is your second language I'd like to commend your grasp of it.

 

[LouLou]

I thought I better commment in case you read somewhere on here about my son testing positive after negative carrier testing in father. He was only screened for 89 mutations NOT THE FULL +1500 AMBRY TESTS FOR.

I have cf. Dh carries S1235R. My son does not test positive for cf through either sweat or IRT birth levels...only genetically. He is also still considered symptomless albeit we do preventative lung clearance care and treat any cough lasting over 4 days with antibiotics. He also is pancreatic sufficient yet give him ABDEK vitamins with a "it can't hurt" philosophy.

I think you need not worry about cf. At this point the chances of one of the many other than cf issues a baby can have are greater I'd say. Not to add to your worry

Also if english is your second language I'd like to commend your grasp of it.

 

[LouLou]

I thought I better commment in case you read somewhere on here about my son testing positive after negative carrier testing in father. He was only screened for 89 mutations NOT THE FULL +1500 AMBRY TESTS FOR.

I have cf. Dh carries S1235R. My son does not test positive for cf through either sweat or IRT birth levels...only genetically. He is also still considered symptomless albeit we do preventative lung clearance care and treat any cough lasting over 4 days with antibiotics. He also is pancreatic sufficient yet give him ABDEK vitamins with a "it can't hurt" philosophy.

I think you need not worry about cf. At this point the chances of one of the many other than cf issues a baby can have are greater I'd say. Not to add to your worry

Also if english is your second language I'd like to commend your grasp of it.

 

[LouLou]

I thought I better commment in case you read somewhere on here about my son testing positive after negative carrier testing in father. He was only screened for 89 mutations NOT THE FULL +1500 AMBRY TESTS FOR.

I have cf. Dh carries S1235R. My son does not test positive for cf through either sweat or IRT birth levels...only genetically. He is also still considered symptomless albeit we do preventative lung clearance care and treat any cough lasting over 4 days with antibiotics. He also is pancreatic sufficient yet give him ABDEK vitamins with a "it can't hurt" philosophy.

I think you need not worry about cf. At this point the chances of one of the many other than cf issues a baby can have are greater I'd say. Not to add to your worry

Also if english is your second language I'd like to commend your grasp of it.

 

[LouLou]

I thought I better commment in case you read somewhere on here about my son testing positive after negative carrier testing in father. He was only screened for 89 mutations NOT THE FULL +1500 AMBRY TESTS FOR.
<br />
<br />I have cf. Dh carries S1235R. My son does not test positive for cf through either sweat or IRT birth levels...only genetically. He is also still considered symptomless albeit we do preventative lung clearance care and treat any cough lasting over 4 days with antibiotics. He also is pancreatic sufficient yet give him ABDEK vitamins with a "it can't hurt" philosophy.
<br />
<br />I think you need not worry about cf. At this point the chances of one of the many other than cf issues a baby can have are greater I'd say. Not to add to your worry
<br />
<br />Also if english is your second language I'd like to commend your grasp of it.