Each year more than 100,000 children are born with. Or develop a craniofacial condition. Start your own free website. A surprisingly easy drag and drop site creator.

Finding a cure, providing hope, and assistance nationwide. Sunday, December 1, 2013. We believe that simple, yet deliberate, acts of kindness and love have the power to change the world! It also has the power to change the way we experience life and see the people around us. Is about spreading that love to others! Imagine for a moment what the holidays might feel like if you decided to bless others with Random Acts of Christmas! Unfortunately the hospital is unable to accept used toys, but can accept gen.

A California Girl and A Boston Boy. Friday, March 6, 2015. Usborne Very First Reading Books. There are also some reading comprehension questions at the end of each story that she really likes.

If I had to choose one thing to pass down to my children, I would choose to pass down my FAITH. My wish is that they would take that, build upon it and make it even stronger than mine. Tuesday, September 1, 2015. If anyone is even thinking about going to Great Wolf Lodge, I have nothing but amazing things to say about it! After much specul.

Cranio Care Bears are two cranio moms whose sons had craniosynostosis and underwent surgery. We now send loving care packages to families with children facing the same surgery all over the world. We Love Our Cranio Kids! We LOVE all our Cranio kids and babies! Everytime we get an email for a care package request our hearts skip a beat! We just love knowing . Awareness Products now available! We now have some awesome awareness items available on our website. All proceeds go towards our care packages! .

Welcome to Cranio Kids! We would love to meet you and hear about your journey! Your donation helps us. Website donated by Flower Web.

God is our merciful Father and the source of all comfort. He comforts us in all our troubles so that we can comfort others. When they are troubled, we will be able to give them the same comfort God has given us. Tuesday, April 1, 2014. So, we saw the orthotics guy shortly after her appointment, and he got her fitted for a splint.

Monday, July 25, 2011. After 6 nights in hospital we were discharged today! The plastics team came by at 8am and gave us the all clear to go home. Harper had breakfast and a bath then we packed up waited to be discharged. Here is Harper the day before surgery and 6 days after surgery. About 30mins later her right.

Tuesday, March 6, 2012. We are back from Dallas. Our appointment went GREAT! He said its fine and just a suture. He had moved his skull around and this is just the lambdoid suture I am feeling. He said his head is going to be changing a lot over the next couple years and we should expect to feel lumps and bumps. He said it should fade and everything is fine. Dr Fearon will be seeing him every year for the next 18 years. Good thing we love Dallas! And planning his first birthday! Thursday, March 1, 2012.