Congenital Diaphragmatic Hernia has effected our lives FOREVER. I pray that no one else has to see their baby in the condition we did. We are grateful that Tyler is a survivor. HALF of the babies diagnosed with CDH don't live. THAT'S TOO MANY. This birth defect is a huge part of our life. It will never go away for Tyler. He will ALWAYS live in fear that his diaphragm could re-herniate at anytime, causing respiratory failure and possibly death. Please help us raise awareness today!!!! THANK YOU!!!
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