Killian is flipping rocking it this week! Since his G-tube surgery, I hear that he really seems to be feeling a lot better. He had another echo done, which came back still mild to no pulmonary hypertension! And, as you know if you're following the fan page, he apparently loves him some mashed sweet potatoes!
Lindsey said that the first time they put them on his lips, he got really PO'ed (which I can't lie, made me giggle a little). But the second time around, he loved them and now gets tastes of sweet potatoes daily now!
|Sweet potato lips! My eyes are crossed because that camera is in my face...again!|
Our sweet boy has been with us for more than 5 months now. That's 5 months longer than most doctors thought he'd make it. As we continue to inch our way to the door, we'd like to ask for your support, well wishes and prayers in the following matters:
- Please continue to hope and pray for the best as they wean Killian very very slowly off the last bit of drugs he's on. So far, so good, but it can take a turn for the worse at any point.
- Let's all focus together on his mental and physical development. I cannot tell you how encouraged we've been by your inspirational stories of how your little loved ones have overcome the hurdles of underdevelopment. Keep sharing those!
- As always please pray/send positive vibes for the doctors and nurses who care for Killian. We love the ambitious doctors (especially the ones who've help get us this far), but we don't want to push Killian to hard too fast.
- Lindsey has a phone interview in a week or so to appeal the decision that Killian doesn't qualify for disability. PLEASE pray and send lots of positivity that she and Killian get the help they need and deserve.
- I'm personally asking for lots of prayers for my little 20 year old sister who is under an incredible amount of pressure and stress.
Being a young single mother in and of itself would be difficult enough. Pair that with the fact that she is caring for a sick baby...well, it would be enough to make even the strongest person crack. Our family is working hard to help in all the ways we can to prepare the house and to support her, but as I've said before this abnormal situation has become our norm. And as we approach this big change, it's easy to let the pressure get to all of us.
Thank God we are believers and we know that He has a plan, a path and a purpose! We sure do serve an awesome God! And now for some more cute pictures :)
|You know it was my 5 month birthday last Saturday!|
|I'm such a happy baby without that silly feeding tube in my nose!|
|Working on my baby biceps pulling on my vibrating cow Aunt Layna bought me.|
Dad and Kerr-Bear will be there next week! I'm starting to get the itch to go back. It's been about 4 weeks for me. But I'm holding out for when I get the call that he's going home. Can you imagine that day!! I just can't wait!
Have a great week! And follow his fan page for daily updates http://www.facebook.com/pages/CDH-Cherub-Killian/301945533181876. Love you guys!!!
Killian has been fighting - like a champion! - for his life since he was born. Because Killian's family is so spectacular; their friends decided to create this website in their honor to help in any way possible.
We are overwhelmed by the amount of people who have asked for an avenue to help Killian, Lindsey and the family. Any donation made below will go to help pay for food while staying in the hospital, gas back and forth, travel for family and the general care Killian will be receiving beginning on the glorious day he leaves the hospital!
All donations go directly to Killian's care and the care of his family. Also, ten percent of all money collected will be donated to Cherubs, The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support.
More about CDH from CHD Support:
CDH occurs when the diaphragm fails to fully form, allowing abdominal organs into the chest cavity and preventing lung growth. CDH occurs in 1 of every 2500 births; somewhere in the world, a baby is born with CDH every 10 minutes. 50% of babies diagnosed with CDH do not survive. The cause is not known. Over a half million babies have been born with CDH since 2000. CDH is as common as Spina Bifida and Cystic Fibrosis but there is very little awareness and even less research.