Chad and Leslie are proud to welcome little Olivia Grace into the world! (born July 20, 2009)

You can email us at
lesliestevens07@gmail.com or csteven1@gmail.com, or feel free to leave your comments after any of the posts--we'd love to hear from you!

If you haven't already, click on the link for "Olivia's Endowment at Texas Children's Hospital" on the left to learn about “The Olivia Grace Stevens Endowed Fund in Neonatology” we've started at Texas Children's Hospital to help other babies and families in need, and to find out how you can contribute if you're interested.

Saturday, August 22, 2009

We Are...Penn State



Little Olivia and I have been learning about one of the good things in life...Penn State and Penn State Football (and the Houston Rockets.) In the picture above, I'm reading Olivia her favorite book "Hello Nittany Lion" where the Nittany Lion travels to a Penn State Football game past all the "famous" Penn State landmarks like the Nittany Lion Shrine, Old Main, the Creamery, the Nittany Lion Inn, the University Gates and OF COURSE BEAVER STADIUM where he meets Joe Pa! What great childhood reading!

Here's another picture of our sweet pea and her proud papa!



And her Rockets t-shirt with Clutch on it! You'll also notice Snuggles, Olivia's sea horse friend!

Friday, August 21, 2009

Large and In Charge - Olivia hits 5 lbs!

Good news! Tonight Olivia gained 75 grams, to get to 2275 grams or 5 pounds! While not Earth-shattering, it's another major milestone for us. She continues to grow and get healthy.

Olivia is back on her nasal cannula and off bottle feeding, it looks like she wasn't quite ready to master that task. While she has a good suck (so I'm told), she seems to be aspirating a little bit. She'll be on the cannula for the weekend and then we'll see how she does! This is not alarming to us in any way, just a little bump in the road.

On a more happy note, yesterday Olivia celebrated her 1 month birthday. Unfortunately, I had to travel to Philadelphia for work but came home with a birthday present for Olivia, a book "Commander in Leash" about President Obama's dog, Bo. My present was reading it to her, while she looked at me with her eyes, which she's opening a lot more!

Wednesday, August 19, 2009

Bottle Feeding, Eye Opening and Baby Massage

It's been a little while since our last post, so the guilt has finally gotten to me...hence this post.

Little Olivia is doing great, she continues to make progress in all of the areas that are "important." She now weighs 4 lbs. 13 ounces, just 3 ozs. from 5 lbs!!! She continues to learn to open her eyes, is starting to keep them open for a long while and beginning to focus on objects close enough for her to look at. We've also learned how to give baby massages, which she obviously loves. I mean, who doesn't like massages? Even the ladies at the hospital are starting make comments about how spoiled our little Olivia is becoming!

The biggest news is that we're starting to bottle feed our little girl, which is a huge step to getting her home. She started off slow 4 days ago, taking 5-8 cubic centimeters, but yesterday she took all 15 twice! When I fed her in the afternoon, she took the entire bottle then fussed at me because she couldn't get anymore! We know for sure she has her parents' appetite.

Thursday, August 13, 2009

More Big Steps for Olivia!

Miss Olivia continues to make great progress every day, thanks to God and the wonderful staff at Texas Children's. Here are the latest and greatest updates and changes!
  • Olivia got upgraded on Monday from the Level 3 NICU (most intensive) to Level 2! Level 2 is way more laid back, and we are so happy to have her there now--especially because the next move after Level 2 will be to bring her HOME!
  • She now weighs in at 4 pounds 7 ounces (or 2010 grams), so she is getting closer to having gained a full pound since birth, which is exciting! And, she has surpassed the magical 2000 grams threshold at which the doctors start considering sending babies home (assuming they're ready in all other areas as well).
  • Today we started reintroducing Olivia to bottle feeding, as she has been fed exclusively through a tube into her nose for the last few weeks. She didn't finish the whole bottle, but she still did great--she was very interested in her milk and made it clear that she was not happy any time we took the bottle away for even a second! (she is definitely her mommy and daddy's child when it comes to eating...)
  • We've started doing more developmental activities with Olivia, like reading to her and playing musical toys for her. The first time I played her Baby Einstein classical music toy a couple days ago, she almost immediately turned toward it and started opening her eyes!
Here are a couple pictures of Olivia in her "big girl bed" (a.k.a., a regular crib), which she moved into a week ago when the doctors decided she was ready to leave her heated isolette behind:




Here are Olivia and Daddy together a couple days ago, doing our favorite activity (skin-to-skin time):


As always, we want to thank all of you for your continued interest in how Olivia's doing, and all your support, friendship and prayers--it has meant so much to us!

Monday, August 10, 2009

TX Children's Hospital - Our Attempt to Help Future Kids and Families!

Dear Friends and Family,

I am writing on behalf of my entire family to let you know about an endowment we have started at Texas Children’s Hospital on behalf of our little girl, Olivia Grace.

Olivia was born almost 3 weeks ago. During Leslie’s pregnancy, we found out that she was growing slower than most babies and were referred to a series of specialists associated with Texas Children’s Hospital. As a result of those visits, we learned that Olivia really looked like a normal baby, just smaller and with a few issues that we’d need to look into after she was born. Because of these recommendations, Leslie and I opted for Olivia to be born via C-section so that we could have all of the right people there to take care of her in the event that they were needed.

So the big day came! Olivia was born July 20, 2009 at 12:40PM and weighed in at 3 pounds, 11 ounces. That’s when the staff at Texas Children’s started to amaze us with their knowledge and expertise. Right away, a neonatology team whisked Olivia to a prepared area to be evaluated. She had a blockage in her airway and had to have that cleared out. After that, she met her mommy and went to the Neonatal ICU at Texas Children’s. That was Miracle #1 performed for us by Texas Children’s.

Since then Olivia has been watched 24x7 by the great staff at Texas Children’s. Leslie and I have been amazed over and over by their expertise, but even more by how much they truly care about the children they are taking care of.

Olivia’s first few days in the NICU were trying for the entire family, but mostly for her. During that time she essentially had her entire body imaged and evaluated by doctors at Texas Children’s. Among the tests that were performed were: complete blood work, an MRI of her head, an ultrasound of her head, an ultrasound of her heart, an echocardiogram of her heart, an ultrasound of her abdomen, x-rays of her lungs, and complete sequencing of her genes (and chromosomes). So that’s the major stuff, and suffice it to say that a lot of other “minor” work was also performed. In addition, Texas Children’s sequenced our genes, for free. We consider the availability of all of these tests to help little Olivia Miracle #2 in her journey.

Leslie and I and all of our family members were literally beside ourselves as we waited for ALL of these tests to come back. These were literally the worst moments of our lives, as the doctors told us that there was a chance that Olivia had a life threatening condition that she most likely wouldn’t survive from. So we waited, and cried, and waited, and cried, and prayed, and prayed, and cried, and prayed, and prayed, and waited, and cried, and waited. Then, one by one, the tests came back, all positive for us! Of course, minor issues were found, but nothing life threatening in any way and nothing that we can’t manage (I’ll spare the details in this letter, but we’re happy to talk about it). We have nothing but positive things to say about the way the staff at Texas Children’s conducted themselves throughout this ordeal. Like I said before, they did an amazing job with all the medical stuff, but they also cared for us in such a compassionate way. For example, when we heard that Olivia’s condition was not what they originally thought, and thus was not life threatening, just about every one of the Texas Children’s staff was crying as we were crying. I’ll take that and call it Miracle #3.

Since then, little Olivia has been spending her time under the watchful eye of the nurses and doctors responsible for her care and doing the things that little babies do – mostly sleeping, some eating, lots of pooping and a little fussing at her mom and dad. The important thing is that she’s improving every day and hopefully coming home soon!

She’s our little sweetheart, or “sweet pea” as I call her, and she literally wouldn’t be here with us today without Texas Children’s.

We realize that having Olivia in our lives is a miracle and that we wouldn’t have her without all of the care we’ve received at Texas Children’s. That’s why we set up a charitable endowment on behalf of Olivia in hopes that we can, in some small way, help Texas Children’s work the same miracles for other families. The Stevens family is proud to announce Olivia’s endowment, officially named “The Olivia Grace Stevens Endowed Fund in Neonatology.”

Our goal is to contribute the fund’s initial value on our own over the next few years, but we hope that you might consider making a contribution as well. We’ve been blessed and helped by so many people through acts of kindness and prayer on our behalf, and now we hope that we can help others with this endowment. If you are interested in making a donation, you have two options, both of which are easy and tax deductible. Either way, please be sure to reference “The Olivia Grace Stevens Endowed Fund in Neonatology” in the check’s memo line, in an attached note, or in the comments online. The first option is to send a check to our endowment’s administrator, Geri Jacobs, the Director of Planned Giving at Texas Children’s. Geri’s address is as follows:

Texas Children’s Hospital
ATTN: Geri Jacobs, Director of Planned Giving
1919 S. Braeswood MC 4-4483
Houston, TX 77030-4412

The second option is to make a donation via Texas Children’s website, http://www.texaschildrens.org/. If you choose this option, click on “Ways to Give” at the top right of the website. From there you can choose how you’d like to make your gift, but again please be sure to reference “The Olivia Grace Stevens Endowed Fund in Neonatology.” If you have any questions, please don’t hesitate to contact us--we’ll be glad to help!

Please know that none of this money will go towards Olivia’s care, which has already been taken care of. We just want the endowment to help other families in the future!
Thank you so much for taking the time to read this note. We hope that you’ll seriously consider making a gift, no matter how large or small, to help future families and children through difficult times. Olivia literally would not be here with us today without Texas Children’s Hospital, and we’re so glad to have her fussing at us!

We love you all! -- Chad and Leslie --

Friday, August 7, 2009

Milestones, Milestones, Milestones

Wow, since our last post (before the family photos) Olivia has done some pretty amazing things! I'll get right to it...

  • Her nasal canulla, which gave her oxygen through her nose, has been removed. She's breathing the air we breath with no help at all!
  • She's been removed from her isolet (think the baby incubator) and has been keeping her body temperature up!
  • She has started to open her eyes and look around! She opens one eye at a time, just a little bit, looks around and then shuts it. It's so amazing to watch her take in the world for the first time. You can just see her soaking it all up!!! Here's a picture!
  • I'm hoping to not be premature with this one, but Olivia may potentially move from the Level III to the Level II NICU at Texas Children's on Monday if she keeps breathing deeply, so keep your fingers crossed (and pray!)
All of these things, and many others, have led to a few positive days and Olivia continues to trend in the right direction. Every day we get a little more optimistic that she'll be coming home someday soon.

Other than that, Olivia continues to do the things that babies do. She loves being held by mommy, daddy, papi and honey; she loves pooping; she loves eating; she loves fussing at her daddy when he doesn't give her her pacie and most of all she loves sleeping.

Our First Family Photos

After a lot of prodding (thanks mom), we finally remembered that we need to take a family photo! So here they are!


OK - So Olivia's a little unhappy, but still cute

So they're pretty candid, but still our first photos as a family




Tuesday, August 4, 2009

Olivia Continues to Grow

This post won't be long, I promise. For all of those blog and weight (Olivia's) watchers, I just wanted to let you know that little Miss Olivia gained another ounce yesterday, putting her at a whopping 4 pounds 2 ounces. She's averaging about an ounce a day, which would give her about a pound of body weight every 2 weeks or so.

Quick math reminder... 16 ounces = 1 pound = 452 grams (how the hospital weighs her). Who would have thought they'd get a quick math lesson reading our blog.

On a serious note, Leslie and I want to continue to express our thanks to everyone for their thoughts, prayers, food, help, etc. It really means a lot to us and I'm not sure we could survive without it!

Some quick thank yous...(send all complaints above omissions to Leslie). Please note, these are in no particular order and are right off the top of my head.
  • Stephanie and Heli - thanks for your constant support, both in and out of the hospital. Oh yeah, the food is awesome too!
  • Mom and Dad - even though you're far away in gloomy Pennsylvania, it has helped so much to have you to talk to. I know that your "Olivia Updates" are necessary and being spread far and wide throughout northwest PA.
  • Lisa and Peter - for your support too! And for everything you've done at the Ronald McDonald House her and in JAX! Can't wait to see you both soon.
  • Kara and Dave - for the awesome string casserole (so good that I'll put the recipe on here!) and for checking in on us and the house!
  • Our friends in Houston - thanks for all of the offers for help, I promise that we will be taking you up on these offers!

Monday, August 3, 2009

Olivia is Two Weeks Old!

I can't believe time has passed this quickly, but our little sweetheart is two weeks old today! Last Monday we happened to look up at the clock right at 12:40, which was exactly one week after she was born, so maybe we'll do the same thing today. :-)

Olivia is doing great--she is putting on weight every day, usually 1-2 ounces each time. And a couple days ago she hit a big milestone...4 pounds! Now she's a bit over 4 pounds and just continues to grow. Like Chad said, we are a bit obsessive about her weight, but we can't help it--it's just a really good indicator of how she's doing overall, and every ounce gained is one ounce closer to us being able to take her home with us. Another thing that makes us feel really good about her progress is how hands-off the nurses have been with us lately. They have other babies in the NICU that require a lot more attention than Olivia does, so basically they just let us take care of most all of her needs, and they really only step in when it's absolutely necessary. Another good thing about this is that it's building up our confidence level for that day when we do take her home!

Here are a few cute pictures...First, Olivia in her all pink outfit (well, one of many all pink outfits). The hat belongs to the NICU and is huge on her, always slipping down over her eyes, but it does keep her little head warm so it gets the job done.

This picture is from when she was just a few days old, so she's grown quite a bit since then, but I just love the little pose she's doing with her hand up by her face--this has been one of her favorite poses! And the little red bow that our nurse put in her hair was so cute, although eventually it fell out. :-(


Here are Olivia's "Papi" and "Honey" Contreras holding their first grandchild--and yes, they are smitten. :-)


And finally, here is Chad holding our precious sweetpea, doing some skin-to-skin time, or "kangaroo" time, with her. It's amazing just how beneficial this can be to small or sick babies--I don't think doctors even fully understand why, but they have proven time and time again that babies who are held and touched often by their parents do so much better than those who are not. So we try to do as much of this as possible every day, basically just trading her back and forth between the two of us for hours. Plus, we just really love holding her!


I just want to thank all of you again for your continued thoughts and prayers for us and for sweet little Olivia. God has truly carried us through the last two weeks, and all the prayer being sent up on our behalf by our family and friends has been a huge part of that. And the results are tangible--she is doing great! So we will just continue loving on her, praying for her, watching her grow and develop every day, and looking forward to the day sometime soon when we can bring her home with us!