Hi, new to this forum! I am a mum to Olivia with cf she is 4 years old and keeps very well! We live in Northern Ireland and get great support from our local cf hospital. We also have Niamh who is 8 without cf and new baby Eimear who is 4 months. At 12 weeks we had a test done which ruled out cf but the baby will be a carrier. When Eimear was born, and even now, I was obsessed when she would sneeze,cough or sniff!! It is just that her dad doesn't do this, he is so relaxed.I know that she doesn't have cf but<img src="i/expressions/face-icon-small-cool.gif" border="0"><img src="i/expressions/rose.gif" border="0"> I can't help myself. I was wondering if anybody else ever felt the same?
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siblings without cf
- Thread starter michelle1
- Start date
Hi, new to this forum! I am a mum to Olivia with cf she is 4 years old and keeps very well! We live in Northern Ireland and get great support from our local cf hospital. We also have Niamh who is 8 without cf and new baby Eimear who is 4 months. At 12 weeks we had a test done which ruled out cf but the baby will be a carrier. When Eimear was born, and even now, I was obsessed when she would sneeze,cough or sniff!! It is just that her dad doesn't do this, he is so relaxed.I know that she doesn't have cf but<img src="i/expressions/face-icon-small-cool.gif" border="0"><img src="i/expressions/rose.gif" border="0"> I can't help myself. I was wondering if anybody else ever felt the same?
Hi, new to this forum! I am a mum to Olivia with cf she is 4 years old and keeps very well! We live in Northern Ireland and get great support from our local cf hospital. We also have Niamh who is 8 without cf and new baby Eimear who is 4 months. At 12 weeks we had a test done which ruled out cf but the baby will be a carrier. When Eimear was born, and even now, I was obsessed when she would sneeze,cough or sniff!! It is just that her dad doesn't do this, he is so relaxed.I know that she doesn't have cf but<img src="i/expressions/face-icon-small-cool.gif" border="0"><img src="i/expressions/rose.gif" border="0"> I can't help myself. I was wondering if anybody else ever felt the same?
Hi, new to this forum! I am a mum to Olivia with cf she is 4 years old and keeps very well! We live in Northern Ireland and get great support from our local cf hospital. We also have Niamh who is 8 without cf and new baby Eimear who is 4 months. At 12 weeks we had a test done which ruled out cf but the baby will be a carrier. When Eimear was born, and even now, I was obsessed when she would sneeze,cough or sniff!! It is just that her dad doesn't do this, he is so relaxed.I know that she doesn't have cf but<img src="i/expressions/face-icon-small-cool.gif" border="0"><img src="i/expressions/rose.gif" border="0"> I can't help myself. I was wondering if anybody else ever felt the same?
Hi, new to this forum! I am a mum to Olivia with cf she is 4 years old and keeps very well! We live in Northern Ireland and get great support from our local cf hospital. We also have Niamh who is 8 without cf and new baby Eimear who is 4 months. At 12 weeks we had a test done which ruled out cf but the baby will be a carrier. When Eimear was born, and even now, I was obsessed when she would sneeze,cough or sniff!! It is just that her dad doesn't do this, he is so relaxed.I know that she doesn't have cf but<img src="i/expressions/face-icon-small-cool.gif" border="0"><img src="i/expressions/rose.gif" border="0"> I can't help myself. I was wondering if anybody else ever felt the same?
M
Mommafirst
Guest
My youngest is my CFer, and I know that my other two are just carriers, but still I always wonder if I'm missing something. You are not alone.
M
Mommafirst
Guest
My youngest is my CFer, and I know that my other two are just carriers, but still I always wonder if I'm missing something. You are not alone.
M
Mommafirst
Guest
My youngest is my CFer, and I know that my other two are just carriers, but still I always wonder if I'm missing something. You are not alone.
M
Mommafirst
Guest
My youngest is my CFer, and I know that my other two are just carriers, but still I always wonder if I'm missing something. You are not alone.
M
Mommafirst
Guest
My youngest is my CFer, and I know that my other two are just carriers, but still I always wonder if I'm missing something. You are not alone.
PlumPerfect
New member
I wonder allot with my older on with out cf. we did a sweat test which ruled it out with low numbers... but i still always have it in the back of my head...
PlumPerfect
New member
I wonder allot with my older on with out cf. we did a sweat test which ruled it out with low numbers... but i still always have it in the back of my head...
PlumPerfect
New member
I wonder allot with my older on with out cf. we did a sweat test which ruled it out with low numbers... but i still always have it in the back of my head...
PlumPerfect
New member
I wonder allot with my older on with out cf. we did a sweat test which ruled it out with low numbers... but i still always have it in the back of my head...
PlumPerfect
New member
I wonder allot with my older on with out cf. we did a sweat test which ruled it out with low numbers... but i still always have it in the back of my head...
Augustmom0003
New member
You're not alone. My daughter had a sweat test after my son was diagnosed and although it was normal, it was a high normal. This wasn't good enough for me - the natural worrier. I finally broke down and had her genetically tested. She is a carrier...but it was the BEST feeling in the world to know I didn't have to worry anymore!!!!
Augustmom0003
New member
You're not alone. My daughter had a sweat test after my son was diagnosed and although it was normal, it was a high normal. This wasn't good enough for me - the natural worrier. I finally broke down and had her genetically tested. She is a carrier...but it was the BEST feeling in the world to know I didn't have to worry anymore!!!!
Augustmom0003
New member
You're not alone. My daughter had a sweat test after my son was diagnosed and although it was normal, it was a high normal. This wasn't good enough for me - the natural worrier. I finally broke down and had her genetically tested. She is a carrier...but it was the BEST feeling in the world to know I didn't have to worry anymore!!!!
Augustmom0003
New member
You're not alone. My daughter had a sweat test after my son was diagnosed and although it was normal, it was a high normal. This wasn't good enough for me - the natural worrier. I finally broke down and had her genetically tested. She is a carrier...but it was the BEST feeling in the world to know I didn't have to worry anymore!!!!
Augustmom0003
New member
You're not alone. My daughter had a sweat test after my son was diagnosed and although it was normal, it was a high normal. This wasn't good enough for me - the natural worrier. I finally broke down and had her genetically tested. She is a carrier...but it was the BEST feeling in the world to know I didn't have to worry anymore!!!!