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-   -   Update (x-posted) (http://www.justmommies.com/forums/f789-our-pregnancies-and-our-earth-angels/2385873-update-x-posted.html)

~Laurie~ August 1st, 2011 03:46 PM

Update (x-posted)
 
Sorry it took so long for me to update you all. I've been spending most of my time at the hospital. Chloe is doing very well with all the usual preemie troubles. She has been off CPAP since Wednesday, she is handling her feeds and eliminating well and putting on weight (she is almost 3 lbs!), but the liver issues continue. They did an MRI on Wednesday and I overheard the doctors talking about a possible diagnosis. It seems she has iron deposited in her liver and a little in her spleen and vertebrae. This can be a sign of poor placental function or something called Neonatal Hemochromatosis, which is very rare and very bad. After I overheard that I went home and Googled it (naturally) and proceeded to lose it. It's hard to read "usually fatal" in regards to your own child. NH usually results in stillbirth or fetal death in the first weeks or months following birth. It is alloimmune rather than autoimmune (not that I fully understand the difference), but ultimately it is caused by something in the mother. It has an 80% reoccurence rate after the first NH baby. It results in placental edema (which I've had for both my losses and Chloe), low amniotic fluid and ascites (which was the case with Chloe). I called and asked for a meeting with her doctor (whom I love) and he said that he didn't want me to hear that name because he knew it would freak me out. He said it is only one possible diagnosis and, if that is what she had, it would be the first case he'd ever seen. She is under the care of a liver specialist. Currently she is doing well (off the CPAP, feeding well, liver functions and coag numbers are up, bili is down) so we are hoping that she just continues on this course. It is difficult to positively diagnose NH without a liver biopsy, and I don't know that I would sign off on that.
I can't lose her and I am so frightened and stressed, but I am trying to stay positive. Please don't mention any of this on Facebook.

http://cimg3.ibsrv.net/gimg/www.just...ee4411fe30.jpg
http://cimg4.ibsrv.net/gimg/www.just...f93e7e78de.jpghttp://cimg5.ibsrv.net/gimg/www.just...242eb0b9d3.jpg
http://cimg6.ibsrv.net/gimg/www.just...1137a31fdd.jpg

noworries August 4th, 2011 07:27 PM

Re: Update (x-posted)
 
Praying hard for sweet baby Chloe. She is absolutely gorgeous. I'm glad that she is doing so well and praying that NH is not the diagnosis. Praying for strength and comfort for you to as you deal with all of this.

Elsa August 5th, 2011 09:56 PM

Re: Update (x-posted)
 
She is sooooo beautiiful and so are you! I'll be praying so hard for your little sweetheart. I hope she continues to improve.

helen123 August 6th, 2011 01:10 AM

Re: Update (x-posted)
 
She is gorgeous. I'll be thinking of you and your little one. Hope she'll continue to improve.

liz bevan August 7th, 2011 03:14 PM

Re: Update (x-posted)
 
she is beautiful.
keeping you all in my prayers


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