Congenital Diaphragmatic Hernia Awareness Month 2023

Congenital Diaphragmatic Hernia

CDH is a birth defect that occurs when a baby’s diaphragm (a thin sheet of muscle that separates the abdomen from the chest) fails to fully form, allowing abdominal organs to enter the chest cavity and prevent lung growth. CDH occurs in approximately 1 in 2500 births, with over 1600 babies diagnosed each year in the United States alone. There is currently no known cause.

84 Countries, Dozens of CDH Charities, and 1000’s of CDH Families, Friends and Researchers Unite to Raise Congenital Diaphragmatic Hernia Awareness

2023 CDH Awareness Day Events

Congenital Diaphragmatic Hernia Awareness Day is April 19th and is recognized by patients, hospitals, charities, and governments around the world!   Click here to learn why this day was chosen.

Go see light-ups, participate in fundraisers, hold your own event, and more by clicking the button below!  

CDH Awareness Day Light Ups

View the list of landmarks around the world that will be lighting up on or around April 19th to raise Congenital Diaphragmatic Hernia Awareness! Make sure to participate in our Dinner by CDH Light initiative to raise more awareness and funds for the children!

2023 CDH Telethon

Every year we go live for up to 12 hours raising Congenital Diaphragmatic Hernia Awareness and funds to help the kids! This year we have 3 co-hosts, including a celebrity!
Join us on April 30th at 9:00 am EST as CDH families share their stories, researchers give us updates and celebrities make guest appearances!

2023 CDH Awareness Proclamations

Every year, states, provinces, and towns proclaim April as “Congenital Diaphragmatic Hernia Awareness Month”.  The United States Senate has proclaimed April as “Congenital Diaphragmatic Hernia Awareness Month” many times!

View the list of 2023 proclamations and learn how you can ask your mayor to write one as well. 

Virtual CDH Awareness Ribbons

Every year we post the names of all the CDH patients who are members of CDH International and who give permission to be listed.  Scroll through the 1000’s of names and donate $5 to add an addition ribbon by the name of someone you love born with Congenital Diaphragmatic Hernia to help us serve more patient families in their time of need.

Fundraise for CDH International

Our organization is able to provide resources, unbiased and accurate information, support services, and research because of our wonderful donors and fundraisers.   Please consider holding an event or creating a Facebook Fundraiser in honor or memory of someone you love born with Congenital Diaphragmatic Hernia.

Donate to Fight Congenital Diaphragmatic Hernia

CDH is one of the most expensive and least funded birth defects. Funding is needed for research, awareness efforts, family support services, patient expenses, funerals, scholarships, and more.

CDHi is a registered charity in the US, UK, Canada, Switzerland, Netherlands, Hong Kong, and Singapore.

CDH Awareness Tartans

In honor of the CDH Study Group meeting in Scotland in April, as well as the Scottish Government Approval of 2 Congenital Diaphragmatic Hernia Awareness Tartans, we will be celebrating with a lot of CDH tartan this year! 

CDHi is selling over 200 tartan items.  Order your items for CDH Awareness Day now to have them by April 19th!

Recommended Articles

Translate »