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Originally posted by Alliance
And many of those disorders have treatments. And many of those children will have lifespans well into their late 30's. I'm sure thier lifespans will increase dramatically as more research is done.
Many of these disorders have treatments which are in essence palliative care. Which disorders are you referring to?
Someone with Cystic Fibrosis has an expected lifespan of around 35 years. Someone with Down's Syndrome has an expectancy of around 50. Someone with Huntington's can live a relatively long life and not manifest symptoms until they're around 50.
These people whence born can lead fulfilling lives, despite the debilitating effects and complications of these illnesses, true.
But let's not confuse things; at the stage we are referring to these are not children, they are a zygote, blastula, morula, or foetus.
I have no qualms with someone who tests positive for Huntington's using IVF and preimplantation screening to detect against Huntington's. I have no qualms with a couple in their 40s opting for an abortion after CVS or amniocentesis reveals the foetus has a trisomy 21. These are not my decisions to make, nor my place to judge.
Originally posted by Alliance
Just because there aren't tests now, its not relevant? I dont think so. You are nieve to dismiss such prosepects. Designer babies have been ethical issues in American culture for well over 50 years.Its a serious issue. Where do you draw the line? And ignorance does not make the need for a line to go away.
I didn't say it wasn't relevant, I said that a barrier exists preventing it. Although on the relevance, an ethical debate over the use of genetic screening methods to detect against polygenic traits
is premature when the means to do so are not in the immediate foreseeable future.
I am being naive. While to be sophisticated and worldly one must engage in prophetic doom-mongering of a slippery slope to the Third Reich. The current use of cytogenetic screening techniques for illnesses, and the potential for parents to opt not to carry these foetuses to term upon the results of these tests; does not imply the development of such screening techniques to be used on polygenic variable traits, nor does it imply that such screening techniques should they exist would be legal, nor does it imply should they be legal that they would be unregulated, nor does it imply should these techniques be readily available in an unregulated fashion that they would be utilised widespread by the public.
The ethical issues of solely the American culture for the past 5 decades are not my concern - this is not an "American issue". The ethics of the scientific community as a whole are robust, and the capacity of the community for self-regulation is inherent.
To whom are you referring as ignorant?
I'm not going to draw some arbitrary line, I'm not a legislator nor a medical practitioner nor a carrier or sufferer of the debilitating disorders one may not wish upon their own children.