Impatiently Waiting for our Miracle(s)

I've been pretty quiet over here lately. Truth is, I'm somewhere in between wanting to soak up every single second I have with these babies (and making the most of what free time I do have) and knowing I have an amazing opportunity to educate others on post transplant and post "trying-to-conceive" life. And I struggle with sharing the hard days because as hard as some of them feel, I constantly have a voice in the back of my head saying, "but these struggles are for good reasons". As we get closer to Christmas I have such mixed feelings. I have butterflies in my stomach thinking about the fact that this is our first Christmas with not one but TWO babies. And Reid is almost one year post liver transplant (how is that possible?!) And then I think of all of the families, the Sparks in particular, that will be experiencing their first Christmas without a loved one. And the couples who thought for sure THIS would be the Christmas that they'd have a baby in ...

Let me tell you about a little girl who has stolen our hearts, but almost never came to be. After three natural pregnancy losses and two rounds of IVF (in-vitro fertilization), we started our third round of IVF in the summer of 2018. Two of our pregnancy losses were due to chromosome issues so we did PGS (Pre-implantation Genetic Screening – checking the chromosomes of embryos for abnormalities) testing for our first two rounds of IVF. All (4) of those embryos were deemed “abnormal”… they either had an extra chromosome or they were missing one. And they were all issues that were not compatible with life. So going into round 3 we were looking for a “fresh start”. To our surprise, our doctor (who is amazing at thinking “outside of the box”) suggested we forgo the PGS testing for our 3 rd round. Each of our chromosome abnormalities, including two of the pregnancy losses, were all different abnormalities (it was a different chromosome missing or extra each time). So he thought it wa...

Today marks one month since Reid was wheeled into the Operating Room for his liver transplant. One month since our lives changed forever. That was the best day, but I’ll be honest – it was also the hardest day of my life. I don’t think we were fully prepared for the emotions that would surround that day. And it’s just now catching up to us that this happened. One month ago he received the ultimate gift. He received the gift of life. The gift of not living with his disease, Primary Sclerosing Cholangitis, and all of the symptoms that came with it. The gift of not having to worry every day that cancer was taking over his liver. The gift of looking forward to watching his babies be born, and not having to worry how long he’d be around to raise them. The gift of no longer wondering whether he would ever get the liver transplant he needed. An absolutely priceless gift. I don’t even know that I can properly vocalize the emotions we felt in the 33 hours leading up to him being taken bac...