CDH Help
So I have started this blog for two reasons.
1. My sister, Angela, told me to.
2. To provide information and support to CDH parents and children and for those who are just finding out their baby has CDH.
When I first found out Kayla had CDH I had no clue what it was. I searched on the internet and didn’t find much. The only site I really found to help a little was the CHERUBs site. But what has helped me more than anything are the blogs that you keep. Reading about your journey with your CDH baby has helped me to see what I may face in the future and just to be able to know what you are going through, sympathize and try to help as you have done for me.
So my main goal is to have this site pop up when you do a google/yahoo search for CDH. My brother has done a lot for me for this site and will make this happen.
I just really want to help CDH families and those who don’t know they are a CDH family just yet- I believe this is good therapy and I think a lot of you out there may too.

Hello I’m glad you want to raise awareness and educate people about CDH but I think it is important for you to ask people before putting their blogs on your site. This is their personal space…even though it is public. Please ask first, thank you.
~Terri L. Helmick
As a new mom expecting our first baby who has LCDH, thank you for doing this! It is a huge help to have the support from families who have been down this road already. It is so encouraging to see and read about these babies who have beat all odds and are having fun in life! Thank you!