"10 years ago when given the diagnosis that our unborn daughter, Kaleigh, was going to be born with a Congenital Diaphragmatic Hernia (CDH) my husband and I felt utterly helpless. Thankfully I found CHERUBS while searching the internet for anything and everything about CDH. They became my support system and got me through the roughest of days, especially after Kaleigh passed away at 17 days old due to CDH. They are still my support system and despite the little funding they receive from donations I always know that someone will be there to pick me up on the worst of days" - Karen Myers, mother to Kaleigh
http://www.cherubs-cdh.org/
No comments:
Post a Comment
Please feel free to leave comments. Comments are moderated to protect our site from spammers and trolls and to keep a positive atmosphere for CDH families. Comments are public.
You may contact us confidentially at cpab@cherubs-cdh.org