Seeking Advice/Input

Kristen

New member
Thank you for apologizing for the tone of your "yelling" post. I wasn't going to respond to that post, but I would like to respond to you now. I understand your feelings and think you have very valid reasons for feelings them.

As a woman with CF who decided to get pregnant, I would like to answer some of your thoughts from my point of view.

"I simply do not understand how someone with CF would risk their own health to birth a child who also may become a carrier or born with CF "

Personally, I am very healthy and I talked to my doctors about the risks I would be taking if I got pregnant. I also read the research. As a matter of fact, the research shows that women with CF who have good health before getting pregnant usually have healthy pregnancies. I decided the risk was low enough to be worth taking. And pregnancy didn't affect me at all - my FEV1 stayed at 113% though out my entire pregnancy.

As far as creating a child who will be a carrier, my husband and I also decided this was worth the risk. Yes, there is some research that shows being a carrier may have an impact on health, but I am a bit skeptical of this mostly because of what I have observed in my own life: Both of my parents are carriers, as are some of my grandparents, aunts and uncles, and cousins and they do not have any CF symptoms. IMO, the biggest impact being a carrier has on my daughter is that she has a 1/25 chance of marrying another carrier, which means she might have to make serious decisions when it comes to having her own child. Again, we decided a 1/25 chance of her having to do IVF/PGD or adopt was worth the risk.

Why didn't we adopt? Well, for selfish reasons. The same reasons that millions of people decided to have their own children. It was very expensive and we wanted our own child. We wanted a baby that we could raise from the moment it was born. We didn't want to have worry about our child being taken from us.

So, I hope that answers some of your questions. You may not agree with my decision to have a child, and that's fine with me (however, the downright nastiness of some other people (not you) is not okay with me). Not everyone is going to agree with my decision, and I am not trying to change your mind, but maybe now you can have a little more understanding.
 
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littlemisssilly

Guest
TheAmazingBD, thanks for your apology / response. You are entitled to your opinion, it was the way you worded your first posts that stirred up emotions in me that made me feel like I had to defend mysdlf. I always feared comments such as yours throughout my pregnancy, even going back to when we started IVF. I was always terrified that people would judge me the way your post did but, I received nothing but support from all those around me. I never expected such judgment to come from a fellow CFer, it really threw me.

I agree with you that CF is an isolating illness, it's incredibly isolating. We're the same age, I went to those camps too but I guess now all we have is these forums.
 

just1more

New member
For those of you that commented on this thread....

The original poster has not been back to our site since this thread went from a honest question, to a heated emotional debate.

Obviously, I think it could be argued that we probably failed to help the OP other than to confirm that there is no civil answer.

If anyone wishes to debate the pros/cons of this topic please create a new topic under the adult forum and keep it civil and you can share your thoughts.
 

sweetninis

New member
Hi me and my husband are also carrier of CF Df508 and we didn't know it till our daughter came in the world with CF.she is my world in my opinion its not wrong to bring a child even when u know you both are cf carriers bc its in God hand your child can be a carrier or if u r lucky can be normal as well you never know.so stay hopefull but let me tell u that u should be prepared mentally financially and emotionally for a child to bring in this world.because its not a joke its a great responsibility
 
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