It's a New Year....(okay well a few days into a new year)
Time for....
New Goals
New Experiences
New Obstacles to Overcome...(and some NOT so new, but we will have to get through them anyway!)
New Memories to Make
New Friendships to Grow
New Trips to Look Forward To
New Things to Organize
New Memories to Make
New Fun to be Had
New Decisions to Make and...
....Many New Stories to Share (and I'm really, really going to try to keep up on this blog more)!
I'm looking forward to many things this year has in store for us, nervous about some parts, grateful for so much, and happy to spend a great year with FABULOUS people!!!
HAPPY 2012!!
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... all about our crazy, wonderful, "perfect" little life
Our Family
Drew Dylan
Addison Malyn
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Our Story
I first began this blog as a way to share pictures and experiences with our family and friends who live far away. I wanted to be sure that everyone could be a part of our lives as Drew grew up. On March 29th , 2008, we were blessed with a beautiful baby girl, Addison. At only 10 days old, Addie was air-vacced to Phoenix and diagnosed with Shone's Syndrome. This is a Congenital Heart Defect which consists of four different and complex complications including: Moderate Hypoplastic Left Heart, Mitral Valve Stenosis, Coarctation of the Aorta and a Ventricular Septal Defect. Addie underwent her first surgery, the new Hybrid Procedure, on April 19th and her second surgery on August 19th. They are planning on Addison having another surgery during the first 2 weeks in September. If all goes as planned, we will be able to go home after that and have a year and a half with her until her next (and hopefully final) surgery at the age of two. So now, this blog has an additional purpose, to take you all on our journey through Addison's progress and give you a chance to watch Drew grow up way too fast!
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