Hi Linds and wheezie - I agree with TONS of what you're both saying. My wife will be getting screened before we attempt a pregnancy, and if she is a carrier, we will not have biological children.
In terms of the article, newborn screening is universal in several states, and carrier testing is "available"... I don't know what percentage of people are getting tested before they have children, but when I read it it seems like more of the effect is coming from newborn screenings. Of course, it may also be happening that once parents know the results of the newborn screening test they may make the decision not to have any more kids, where in the past there would have been a greater likelihood of multiple siblings with CF... that does seem to be rarer these days. I do agree that some of these cases stem from people being very responsible adults.
I also don't have a problem with the technology, and I don't think that all medicine equals "playing god". I do think that some ethical issues come into play with this application of the technology that aren't USUALLY present in the treatment of an illness. For example, do you think that this use of the technology passes the Hippocratic oath? I don't have an answer... part of me says yes, part of me says no. We as people can use our knowledge and ability for good or bad.... does this "feel" good or bad to you? To me this "feels" bad.
Like wheezie, I am most troubled by the social implications of the article. When I read it, I didn't think so much of society as intolerant, but more a reflection of our society's values of instant gratification of our wants, avoiding the difficult or painful, and not appreciating the different, the difficult, or the reward that comes from stepping off the "easy" route.
Chris
27 m w/cf