They biopsied all seven of our embryos today, and have completed half of the testing.
PGD checks for the 10 most common aneuploidies (wrong number of chromosomes - anything but 2 of each). Today, they looked at five chromosomes - 13, 18, 21 and, um, 2 others that I forget. (Maybe X & Y?)
Six(!) of the embryos checked out okay for those five, and one had 3 copies of chromosome 13*.
Tomorrow, they check these remaining six embryos for five more chromosomes and will call and let us know how that went.
For a little perspective:
According to our lab's website, for women 37+ years old, 50% of all embryos show aneuplody for chromosomes 13, 18, 21 or X/Y.
Of embryos that are normal for those chromosomes, another 12% are aneuploid for chromosomes 1, 16 or 22. (I'm guessing they'll be covered in tomorrow's testing.)
Shrike is about eight weeks shy of her 39th birthday, and less than 14% of the embryos failed the first test; so far all indications are that she's made some pretty decent eggs for an old lady!
*For even more perspective:
I did a bit of research on Trisomy 13. Here's what Dr. Google has to say about it:
"The syndrome involves multiple abnormalities, many of which are not compatible with life. More than 80% of children with trisomy 13 die in the first month."Shudder.
We knew that it was pretty much a given that some of the embryos would be chromosomally abnormal, and we knew that, without the testing, there was a chance of an abnormal embryo being tranferred - and being born - but actually hearing these results makes that possibility seem a lot more real.
I do feel a little sad for that one that didn't make the cut today but, more so, I am relieved that we found out about it now, and were able to eliminate it from the pool of potential transferees.
My overwhelming feeling is of having dodged a bullet, which is worth way more than the $3500 that we're paying for the PGD.
Sorry to hear about the little peeplet, but thrilled that the others are faring so well. Keep us updated.
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