Peterson Plus One!

Wow, it has been eons since we’ve made a post on this blog. Sorry for the delay!

Megan continues to grow into a strong little kiddo full of smiles and an easy disposition. We are amazed daily by the speed at which she learns new things. She’s now rolling over both ways, grabbing everything (and putting it in her mouth), sitting up (kinda – this one still needs some improvement), scooting all over as she tries to figure out crawling, and eating baby food. She’s a big fan of sweet potato and carrot flavor baby food, but apple sauce still elicits a gag or two.

We’re getting to a point where we want to film virtually everything and the little video setting on our photo-camera just wasn’t cutting it anymore. Not particularly interested in paying $700 for an HD camcorder, I bought a great little HD Flip (www.theflip.com). This thing is the coolest – it shoots HD footage, up to 2 hrs of filming time with no tapes of memory cards, built in USB and HDMI all for less that $200… but I digress… and I’m a nerd.

We’ve had the little camera for about a week now and shot a bit of Megan footage so I thought I’d put together a short little video montage for all to enjoy. You’ll see that Meg gets a kick out of mama’s fake cough, particularly when she’s eating her cereal. We also caught her first attempts at sitting on camera (while transfixed by football on the TV above her). The last little bit is her doing her Mister Ed impression. I think she’s communicating with us through her little stomping actions. You may notice that Tucker the dog appears very briefly in the film, so I felt compelled to list him in the ending credits. Oh, and note that Megan particularly enjoys the taste of her high chair.

We inadvertently made Megan laugh hysterically this afternoon. I was raising my arms over my head and when I dropped them she initially acted startled, but then began laughing uncontrollably. Fortunately, we were able to capture her first big laugh on camera. Hopefully this is the first of many more (I’m sure she’ll spend a lot more time laughing at her dad throughout her life).

We’ve been talking about buying a camcorder new for a few weeks, but we haven’t bitten the bullet yet. In the interim, we decided to shoot a few short videos on our regular camera. This is Megan smiling at daddy right before her Sunday bath (unfortunately, our camera can’t shoot more than 30 seconds, so it’s a short snippet). She’s already growing out of her little sink-tub and will be bathing in the big kids tub soon.

On a somewhat different note, Megan went to the pediatrician last week and got her first round of shots, which was no fun, but the good news is that she is still looking perfectly healthy (in the 95th percentile actually). She weighs 12 pounds and is 24 inches long – she’s growing like a weed! We’ve also graduated from the apnea monitor since she’s never had a legitimate alarm, so no more wires and buzzers.

How can that not melt your heart?! What a smile!

It has been quite some time since my last post and we have received some terrific news. Megan had her one month follow up with Dr. Rivera, our pediatric neurologist at Texas Children’s, yesterday. He did a thorough check of her reflexes, responsiveness, and a head measurement. He said that she looked absolutely normal and that he believes that her hemorrhage has completely resolved itself. As a final confirmation, he scheduled a ultrasound for this morning to make sure that she was indeed fine. He said that if the results come back clear, we are “home free,” the two most beautiful words I’ve heard in a long time! So at 7:15 AM this morning Megan had the ultrasound. Her brain looked so normal that the technician had to ask which side of her brain the hemorrhage took place on because both sides looked perfect. The radiologist also reviewed the scan and confirmed that the scan looked totally normal. Although we won’t hear from Dr. Rivera until tomorrow, it looks like we are indeed “HOME FREE!” Praise God! Ellen and I truly believe that God healed our daughter.

I have been thinking a lot about the story of Jesus and the Centurion who asks him to heal his servant. He tells Jesus not to trouble himself with coming all the way to the servant, but simply to say the word and his servant would be healed. Jesus did say the word and of course the servant was healed. The same God healed Megan, he brought wholeness and peace through his tremendous power and willingness – I am so grateful.

Thank you all again for your ceaseless prayer and encouragement. Now I can shift my prayers/anxiety to more pressing things like the year 2025 when she starts driving.

Betty graciously babysat for Ellen and I this morning so that we could go to Worship. We really wanted to go to church today considering that it’s Easter and after all we’ve been through. The service was great and it gave Ellen an opportunity to put her baby dress on Megan (the same on that Ellen and her sister wore home from this hospital). We took this picture in our Easter duds.

Megan continues to do great. She has been a really easy baby so far (minus her first week). She sleeps and eats well and the NICU folks got her on a great feeding schedule that we have just stuck to (2, 5, 8, 11, repeat…).

I’m excited to say that I have nothing of great urgency to report today except to say Happy Easter to everyone and as always thanks for your prayers and thoughts.

Megan is finally home! Praise God. We were released from the hospital today around noon. Our Neonatologist ordered Megan’s CT scan a day early becasue our Neurologist was on site yesterday and they could review it together. After looking over the results, Dr. Rivera (our neurologist) called us and said that there is definitively no more bleeding and the bleeding that did occur is continuing to be reabsorbed by her body. He also felt that the CT scan was so encouraging that we do not need to schedule a follow up ultrasound for a whole month (as opposed to one week as previosly scheduled) and  that a simple weekly head measurements by our pediatrician will suffuce until then. He also gave Megan a 90% chance of recovering with no adverse effects and that percentage will go even higher if her follow up appointment goes well in May.

Since she was in the NICU, she is required to go home with a little heart/respiratory monitor that will alert us if there are any problems. She will have to wear the little monitor 24/7 until our pediatrition tells us otherwise. It’s a little elastic band that goes around her chest with a wire that connects to a small box. If any abnormalities in breathing or heart rate occur a loud alarm will sound. Although somewhat inconvenient and a little scary conceptually, we actually find the little monitor to be fairly reassuring.

Hopefully this blog will trasition from a crisis alert system to a fairly boring little baby blog full of stories about spit-up, dirty diapers, and giddyness about Megan rolling over on her own or saying her first words.

Before that happens however, I want to make a point to thank you all so much for your posts, your prayers, your encouragement, and even your interest. Ellen and I never imagined that this would be what our first baby experience would look like and quite frankly I don’t think we would have chosen it in a million years. Nonetheless, God still selected this experience for us and we praise him for it. We have learned so much and been so humbled by Him in the past seven days. We don’t understand why He let this happen, but we do know, more now than ever, that we serve a living God that loves us with a love we cannot fully understand and plan that we cannot comprehend and that He still listens to our prayers and works miracles.

I have been thinking all week about a scene in Castaway where Tom Hanks, after his rescue, is describing his experience on the island when he was totally hopeless he says:

I had power over nothing. And that’s when this feeling came over me like a warm blanket. I knew, somehow, that I had to stay alive. Somehow. I had to keep breathing. Even though there was no reason to hope. And all my logic said that I would never see this place again. So that’s what I did. I stayed alive. I kept breathing. And one day my logic was proven all wrong because the tide came in, and gave me a sail. And now, here I am. I’m back. And I know what I have to do now. I gotta keep breathing. Because tomorrow the sun will rise. Who knows what the tide could bring?

I struggled to put my hope in God after all that Ellen and I have been through, but as usuall, He has been faithful… he has proven all our logic wrong, and look what the tide brought in!

if we are faithless, he will remain faithful, for he cannot disown himself. ~ 2 Timothy 2:13

Praise God and thank you all for your continued prayers!

We finally spoke to our neurologist, Dr. Carlos Rivera, at Texas Children’s Hospital. He has reviewed the latest ultrasound and spoken with our Neonatologist and he feels that Megan’s current status is the absolute best that it could be at this point. At this moment he believes that there is an 80% chance that Megan will have a full recovery. If all her follow up appointments and ultrasounds continue to look good over the next two weeks that outlook increases to a 90-95% chance of full recovery. We truly believe that God has miraculously healed Megan and all the praise is due to Him for it (and all of you for your prayers).

It feels presumptuous to ask for more prayer, but we would appreciate it if you would keep on lifting little Megan up and ask that God would continue to heal her and that our follow up examinations would continue to be excellent.

As always, thank you all for your continuous support, encouragement and prayers.