The Governor of Tennessee has proclaimed that April 2021 be a month that citizens of the state recognize and raise awareness of Congenital Diaphragmatic Hernia. Join us in raising awareness on CDH Awareness Day, April 19th, and all month long. Thank you so much to the Tanner Family for raising CDH awareness in honor of their …
CDH International’s featured patient of the week is CDH survivor Haze Godwin. Haze is the son of Jeremy and Kalen Godwin and they had this to share about their son’s courageous battle with CDH: “We found out at our 20 week anatomy scan that Haze had left-sided CDH. That was just the beginning of our …
We were honored to virtually attend our first RARE event, RARE 2021.
Click below to see our newest addition to the CDH Awareness Shop!
Click below to see our newest addition to the CDH Awareness Shop!
Click below to see our newest addition to the CDH Awareness Shop!
We were honored to virtually attend this year’s European Rare Disorders meeting as new members of EURORDIS.
CDH International would like to welcome Mellissa Reaves to our Patient Advocacy Board. Mellissa is the new Awareness Co-Team Leader. Mellissa Reaves is a Direct Support Professional that works with assisting individuals with intellectual disabilities. Her daughter was born with CDH in March of 2015. Her family includes herself, her husband Kevin, daughter Allison, son Ryder …
A huge thank you to Shreen’s family and friends for holding a fundraiser for CDH International. You are all vital to winning our fight against CDH!!
A huge thank you to Shawn’s family and friends for holding a fundraiser for CDH International. You are all vital to winning our fight against CDH!!
A huge thank you to Tiffany’s family and friends for holding a fundraiser for CDH International. You are all vital to winning our fight against CDH!!
A huge thank you to Jimmy’s family and friends for holding a fundraiser for CDH International. You are all vital to winning our fight against CDH!!
