A couple weeks after Kayden's delivery, we found ourselves in my OB's office. I had been there so many times in the previous months, the staff felt like family at this point. What I didn't know is that Kayden's karyotype analysis (genetic study) had come back and it showed an anomaly:
More than likely: it's pretty easy to spot, right? Usually you have 23 pairs of chromosomes. Sometime those chromosomes don't translate correctly when the cells are dividing and you end up with one less chromosome or one extra. In downs syndrome for example, a child would be born with an extra chromosome #21, or "trisomy 21". Well, in case you didn't notice, this picture shows that Kayden had "trisomy 8". See the extra chromosome #8?
The pathology report above says that a trisomy of some sort is the most frequent cytogenetic abnormality contributing to pregnancy loss. What my doctor added was that, because so many of Kayden's cells were affected, it most likely meant that my egg had an extra cromosome #8 to begin with. (If it had been the sperm, it would have likely been a "slow swimmer" and wouldn't have made it to the egg first).
Every documentation I could find showed that this type of trisomy 8, (which is a COMPLETE trisomy rather than a MOSAICISM) is "universally fatal"- meaning it's incompatible with life. I started wondering how on earth Kayden survived so long and grew perfectly on track. When he was born, he had no physical manifestation of a genetic disorder. PLUS: when Scotlin had this test done, the sample tissue was taken from his actual body, and Kayden's was taken from my placenta. It wasn't adding up, but my OB didn't know anything about it, so I had to wait to meet with the specialist.
July 25th, I was SO GRATEFUL to meet Dr. Mark Grant in Columbia. I won't detail our whole conversation, but basically he had the same suspicion I had and decided to talk to a geneticist to confirm. So, there I was wondering if I have some crazy problem with my genes that's killing my babies and Dr. Grant rushes in to save the day telling me that he and the geneticist talked and decided that the most likely cause was:
NOT TRISOMY 8!
The only way to be sure would be to exhume Kayden's body and retest using a sample from his body. HOWEVER-they didn't think that was necessary and that because he made it to 27 weeks w/o any abnormalities and had a completely normal growth pattern, the trisomy was most likely confined to my placenta. I said, "Oh, that's a thing...that's possible?" And he said "Absolutely."
So...for years we thought Scotlin died from some awful stroke of un-luck. Then I miscarried and they thought that was just another crappy thing that happened. But as soon as Kayden died, my doctors rushed in to tell me that they think all three of these losses are connected somehow and they put Dr. Grant on the case to figure out why. Yesterday, I had a bucket-load of blood drawn to HOPEFULLY find a cause. Now we play the waiting game for a couple weeks and hope to get that phone call. In this case, we're thinking that bad news is better than no news, because it means there's something detectable that can be fixed.
Until then, we'll just live knowing that our boys are perfect and we're so darn lucky they chose to come to our family.



