Reno was baptized on 5 February 2011. I'm just so proud of the little bugger that he is becoming. Starting this blog has sent me into a frenzy of picture looking. Wow how time flies. It feels like he was just my little bug-my little monkey man-our little nutbrown hare, not so, he's practically grown two more years and he'll be as tall as me for sure :)
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Life's Tiniest Blessings

6 May 2005-It's a memory stamped on my soul forever. I knew something wasn't right, I just had no idea that something was wrong, until she came into the world. Kira was 5 lbs 12 oz and so much smaller than her older brother Reno, who came in at a whopping 9lbs 7oz. I quickly asked the doctor if she was okay. "Yes" she said with a smile on her face, and my fears were subdued, but as I looked at the nurses passing her around cleaning and caring for her, I could not help but hold my breath . . . she looked so frail. It wasn't until Richard came to break the news that she had been taken to the NICU that I came face to face with the reality that my fears had been affirmed. "She just couldn't maintain her temperature", was the reason-for the time. That night was the longest night in the history of KiRsTeN BaiLey. The doctor was calm and collected when he explained that she wasn't reacting like a normal new born. Her legs and arms were floppy, her reflexes were non existent, and she couldn't keep warm even though she was wrapped up tight, and she didn't want to eat. So off to Primary Children's she was going. I cried all night long as I heard the other babies being shuffled from room to room, crying for comfort-it sounded like such a beautiful sound under the current circumstances. I would have given anything to just hear her cry-she didn't do that either. Packed tight into an incubator for transport via life flight-"what? how could this be happening?" is all that I could think of. I never in my wildest dreams thought that I would see my baby like that. It didn't take long for them to check me out of the hospital-I would not have let them keep me there. The pitiful looks that I got from the nurses and staff was more than I could take.
But in that time I know that I was lifted up by something bigger than myself. I remember distinctly the song "You Raise Me Up" coming on the radio as I prayed for the strength to make it. I was on my way for an 1 1/2 hour drive to the unknown, but my body was sustained the pain was nothing compared to the lump that was in my chest, not knowing what was wrong.
It didn't take long to get settled into our little cubby, there is such sadness in a NICU, tiny people struggling for life and scared parents clinging to hope. Straight across from us was baby Fralia, she was born with her intestines outside of her body-her parents had been there for 2 months. How do you keep going like that? There were also the forgottens, so many little babies with no one there to sit by their side. That was hard to swallow-how do you fight, alone so small and frail?
We did this for 2 1/2 weeks. That was enough for me. It was on day 11 that we got our answer. Call it luck-I don't know. The nurse was away from our station and yet another Specialist had come around to see if she could tell us what was wrong. A neuromuscular specialist, she was looking for signs that Kira had muscular dystrophy or something like it. She assured us that this was not the case-"but I might have her tested for Prader-Willi Syndrom" she blurted as she walked away. What was that? No one else there to write it down-or tell us what it was. Richard and I rushed down to the 3rd floor where the parent public computer access was. I'm not sure that we should have typed in the search. The lump in my throat grew ten sizes that moment as I read the clinical signs of PWS. In infancy, low muscle tone,small hands and feet, failure to thrive, thermo-regulatory problems, non-reflexive. It all sounded so familiar and then there was more-Later people with PWS have cognitive delays, low IQ's, Autistic tendencies and an insatiable appetite that can lead them to literally eat themselves to death. The lump was so big that I couldn't swallow. I was awake again all night. We didn't have a diagnosis, but I knew. Even with the assurances that PWS was a 1 in 15,000 live birth disorder and the chances that this was it were small, I knew. So by the time the affirmative came, a DNA test came back showing that Chromosome 15 had a deletion in it. . . a tiny deletion that would change our world forever,the lump had had time to subside. I knew in that moment that I had to find the strength to pull it all together and change.
It was a lot scarier in those moments than life has played out. We were lucky to get the diagnosis early. We know what we are in for. It's almost like getting a manual to take home with your baby. You know what their weaknesses are probably going to be and you change your perspective. In a lot of respects Kira is easier than Reno-who knows what he's going to do or be next. So now we live with PWS. Food has become the nemesis, we have to lock it away, and beat it back at every turn, but we are mostly winning the battle. Kira is amazing-she is truly the sunshine in an otherwise cloudy life. It's amazing how she can make the world smile. She's now 5 almost 6, and while the details of those days are little hazy, they will always live stamped on my soul. It is who I am, the mom of Reno(8) and Kira (5 1/2 PWS) and better for it.

It started here 10 1/2 years ago. I had big dreams and plans of a nearly perfect life with nearly perfect kids (5 or so) with a nearly perfect home and nearly enough time to do all the things that bring me joy. But here I am 10 1/2 years later with a much different journey. A journey that is a lot harder than I thought that it would be. Some days it's so worth it, others I struggle to find the optimism. I thought that maybe putting it out there-all of it, the good with the bad- would help to make this climb more successful. So whether any one else sees this or not, it's me and that's all that I have to offer.