My Nonprofit Reviews

My daughter was born with CDH 8 years ago. She was diagnosed at my 20 week ultra sound and without having these non profit groups to give us the correct info on her diagnosis and the support we have received from them and other families we would have been so lost. We are all so appreciative & grateful to have them!

My daughter was born with left sided CDH, she is now 7 years old & since the time of her diagnosis, my 5 month ultrasound, we have been involved with this non profit, more so over the years as it has grown. It is so nice to be able to connect with other families & know we are not alone. Having their support has made a world of difference to our daughter & us!