I have identical twins. One who had a left sided diaphragmatic hernia and the other who did not. I've been out of touch for the past few years and recently have renewed focus on helping anyway I can with CDH research. My sons are 5 now. I realize there could be a lot of research potential as one is a survivor and the other did not have CDH. I'm a bit overwhelmed by all the research posts but I definitely want to participate. Can anyone help steer me in the right direction to studies that we could qualify for. We recently moved back to Northern VA. Thank you so much.
Stay Connected 
Reply With Quote
