Thank you for visiting. Braydon was diagnosed with Craniosynostosis at his 2 month check-up. I hope that reading his story, it will help out another family going through a similar situation. Also Ethan was diagnosed with Craniosynostosis at 1 week old.

Friday, February 4, 2011

1 - Month Post Op

Wow it's been 1 month since we handed our little guy over to the surgeons.  Braydon is doing great.  His incision was infected, but it seems the antibiotics are doing it's job.  His head shape looks awesome!  We couldn't be more pleased.

Braydon has now said ba ba and da da.  He's sitting in a high chair all by himself now, and he's upgraded to his convertible car seat.  We can also "sort of" drink from a sippy cup.  We are almost through the fruits and then he'll be able to eat anything.  Oh boy!

Heaven help us, because our little boy is growing up so fast.

1 comment:

  1. Your written goal is to help families going through a similar situation. I just wanted you to know that it also helps those of us who went through the situation years ago. I am a CS survivor. Technology wasn't as advanced when I was born, but everyone did what they could and i lived through it. It is so great seeing your child doing well. I pray for you and your family and thank you for this blog.