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The Mind of Olivia Drab

Inside the head of a reproductively-challenged space cadet.

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Name:Ollie

6.28.2004

Broken

My Ob/Gyn called me this afternoon.

According to the genetics testing of the fetal tissue, our daughter had an aneuploidy, a chromosomal abnormality called Turner Syndrome or 45X (instead of the normal chromosomal set, 46XX). It only occurs in females. Without getting too scientific, she was lacking a major part of the chromosomal structure and couldn't survive, although it does sometimes happen. In survivors, there are so many physical, developmental and reproductive problems that are associated. But term pregnancies with this abnormality are rare. Had we made it as far as the CVS testing, the doctor would have informed us of the markers for a chromosomal abnormality and we would have had a very hard decision to make.

The bottom line is that there was nothing that we could have done. Nothing would have saved her. And there was nothing I had done wrong. It was inevitable, even if I'd had the hysteroscopic surgery before the pregnancy and it wasn't because of my age. It doesn't stop the hurting, however. But now it is a different hurt. One that provides a small sense of closure. I just have to accept what happened, hope that it was random bad luck, and even more so hope that it won't happen again.

Our next step is genetic counseling to see if it is a permanent situation. I know from prior karyotyping that both Brad and I have normal chromosomes. As to whether or not there is something else that karyotyping doesn't detect, I don't know. I am sure we will find out through the counseling.

I am still going to have the hysteroscopic surgery to rule out anything else. As we all know, bad situations can travel in pairs. We just want to make sure there aren't any bad silent partners in my reproductive history.

Now I just have to process this information. Process and research. And hope... a lot.

15 Comments:

Jo said...

Well, hell.

I'm thankful you at least got an answer, a little bit of closure. Doesn't make it suck any less, but still.

(I so want to send you a creepy internet hug, but will refrain.)

10:07 PM  
getupgrrl said...

I'm so sorry, for you and your girl. It's heartbreaking and peace-bearing, all at once.

I'm thankful that you got an answer.

10:16 PM  
Tiffanni said...

I don't know what to say that the other 2 already haven't. Just know that you and Brad have LOTS of people thinking about you and hoping for the best! I am glad that you decided to still go ahead with the surgery. Let us all know when you talk to the genetics counselor!
(((HUGS)))

10:33 PM  
jilbur said...

Sweetheart, peace to you. I'm grateful that this info can help move your grief forward.

6:58 AM  
sherry said...

May all the peace in the world find you and your husband right now.

3:01 PM  
suz said...

I'm so glad you got the answers, but I know this must dredge up all kinds of confusion, hopelessness, and hurt. I'm thinking about you! {{HUGS}}

I'm so glad you're going ahead with the hysteroscopy. The new RE will do that, right? I hope they find a cute ute in there with no structure problems, and if there are, they're easily fixed.

4:18 PM  
RainbowW said...

love ya hon. whatever happens, love ya.

10:55 PM  
Anonymous said...

I am so sorry. I do remember that an answer, any answer was comforting in this huge island of unknown.
Lisa

11:07 AM  
Anonymous said...

{{{{hugs}}}}
Evelin

1:27 PM  
Jujube63 said...

Keep the hope, for sure, kiddo. It's going to all come out in the wash.
Give yourself time to process--important.
(((and more hugs)))

8:43 PM  
patricia said...

I am so sorry. When I found out that the girl I lost had Down's Syndrome I was very conflicted. The bottom line is that yet another dream is crushed, and now you live with the fear of it happening again. Even though she had Turner Syndrome, you still lost your precious baby girl. Hang in there.

http://laf.typepad.com

1:01 PM  
Anonymous said...

We found out a few weeks ago that the daughter I m/c'ed had Trisomy 22. So, I understand the feelings. We, too, saw a genetics counselor and found it helpful. There is a test that is more advanced than karotyping called FISH. Using a ultraviolet light it highlights all the the bands located on the arms of the chromosome(s)-- they can do one chromosomes or many. It is very costly and I don't know if it's recommend for Turner's. It might be something to check out.

((Hugs))

Mimi

9:39 PM  
Anonymous said...

Hello,

I happened upon your blog following a link from a link sort of thing, and I wanted to tell you how sorry I am for your loss. I have had a similar situation happen. You're right - it brings some peace to know the cause, but of course doesn't do anything to diminish the grief of your loss. I hope your appt. with the genetic counselor is helpful, and that your emotional healing continues.

Laura

7:42 AM  
T. Carter said...

Fluorescence In Situ Hybridization (FISH) is what they did to our embryos during the PGD. It was $3500 for all the embryos (but it would have been the same if we had had 2 or 32).
Evelin

8:13 AM  
Anonymous said...

I'm sorry Melissa. I've had at least 2 chromosomal losses as well(T18 and 21). I'm glad you can have some closure of sort, but I know the loss is hard nonetheless.

Mommajac

3:39 PM  

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