This will be the fourth year of The Noraholics and we could not be more thankful for the support that has been shown to our family over the last (almost) 5 years. Since the day we received Norah's diagnosis, we have made it our mission to talk about CHD any chance we get. How is it possible that CHDs are so common yet we knew nothing of it until it affected our family?! It is so important to help spread awareness and do everything we can to continue to help fund research. After all, ongoing research is what helps doctors provide the care that our children so need.

We hope to see everyone at the walk this year. It is such a special event for such an incredible cause. And who doesn't want to go to the zoo??

Thank you to all of our family, friends and supporters that are there for us year after year to support our bug Norah and all of the other children and families. We couldn't do this without you!