Tuesday, August 25, 2009
Autumn's Art
Posted by The Novaks at 6:43 PM 0 comments
Remember...
There are so many moments at this stage in Caleb's childhood that I just want to freeze and keep forever. I figured that I should start writing some of them down so that I won't forget.
Posted by The Novaks at 6:18 PM 0 comments
Friday, August 14, 2009
David
A lot of you know that I have a brother named David with special needs. A few years ago he was also diagnosed with dystonia. Dystonia is a neurological movement disorder that causes his muscles to twist and spasm. My parents have been looking into a treatment called Deep Brain Stimulation, and it looks like it's going to finally happen. DBS sounds scary because it's brain surgery, but it could be life changing not only for David but for my parents and youngest brother, John, as well. My mom started a blog this week to keep everyone updated on the process, and I've put a link to it on the side of my blog. Please read it if you have time and pray for David and the rest of my family too.
Posted by The Novaks at 6:53 AM 0 comments
Sunday, August 9, 2009
Walking!!!
It's officially happened! Caleb is walking. Up to this point he would walk a few steps every once in a while, but he would always resort to crawling as his quicker mode of transportation. Then on Thursday he decided it was time to take off.
Posted by The Novaks at 7:35 PM 1 comments
Friday, August 7, 2009
Chocolate Chip Cookies
Posted by The Novaks at 5:32 PM 3 comments