Hello Everyone. We are the Kardiac Kids Support group. This Support Group provides education, support, and encoragment for families with children who have or have had congenital heart defects. Our group makes up of all different types of people with all sorts of backgrounds and situations. We are here as an informational and emotional crutch for families who have been given the news that their child is different and special.
Lets all share stories.. information.. and just be there for eachother. I would love for everyone to start with their story of how they found out about their child. :)
Hi there! I think this is such a great resource to have!! I will gladly post Keegan's story :)
ReplyDeleteThanks Julie. I am working on Evan's. I know it will help us all. Lets swap stories.. dr info and more.
ReplyDeletegreat blog! :)
ReplyDeleteHello!
ReplyDeleteMy family and I are considering a move to Oahu and we have a young son with a Congenital Heart Defect. I found your blog and am looking for more information about the doctors and hospitals on the island. We are currently in Southern California and are members or a great kids heart network. There is nothing like a sense of community when navigating the ups and downs of loving our special heart babies. I would love to talk more if anyone is willing - I can be reached at erica.alvino@gmail.com.
Thank you so much!