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Get ready to raise awareness and take action on Congenital Diaphragmatic Hernia Action Day on April 19! This day is dedicated to spreading knowledge about a birth defect that affects the diaphragm, a crucial muscle in the body responsible for breathing. It is estimated that around 1 in every 2,500 babies are born with this condition, making it important for us to come together and support those affected by it. Let's join forces and show our love and care for those living with congenital diaphragmatic hernia.
<div class='timeline-item'><div class='timeline-left'><div class='timeline-date-text'>1950s</div></div><div class='timeline-center'></div><div class='timeline-right'><div class='timeline-text timeline-text-title'>Early Medical Recognition</div><div class='timeline-text'>In the mid 20th century, medical professionals increasingly recognized and diagnosed Congenital Diaphragmatic Hernia as a severe birth defect.</div></div></div><div class='timeline-item'><div class='timeline-left'><div class='timeline-date-text'>1980s</div></div><div class='timeline-center'></div><div class='timeline-right'><div class='timeline-text timeline-text-title'>Medical Advances</div><div class='timeline-text'>Advancements in neonatal medicine and surgical techniques in the 1980s drastically improved outcomes for babies born with Congenital Diaphragmatic Hernia.</div></div></div><div class='timeline-item'><div class='timeline-left'><div class='timeline-date-text'>2005</div></div><div class='timeline-center'></div><div class='timeline-right'><div class='timeline-text timeline-text-title'>Research Breakthroughs</div><div class='timeline-text'>In 2005, significant progress was made in the genetic research of Congenital Diaphragmatic Hernia, leading to a better understanding of its causes.</div></div></div><div class='timeline-item'><div class='timeline-left'><div class='timeline-date-text'>2010</div></div><div class='timeline-center'></div><div class='timeline-right'><div class='timeline-text timeline-text-title'>First CDH Awareness Month</div><div class='timeline-text'>In 2010, the first Congenital Diaphragmatic Hernia Awareness Month was observed to increase public attention to this little-known condition.</div></div></div><div class='timeline-item'><div class='timeline-left'><div class='timeline-date-text'>Current</div></div><div class='timeline-center'></div><div class='timeline-right'><div class='timeline-text timeline-text-title'>Continued Research and Support</div><div class='timeline-text'>Today, research continues into the genetic causes and treatment options of CDH, while communities around the globe gather yearly to raise awareness and funds for those impacted by this condition.</div></div></div>
<div id='' class='facts-item'><div id='' class='facts-header'><h3 id='' class='facts-number'>1</h3></div><div id='' class='facts-text-wrapper'><h3 id='' class='facts-title'>Wear purple</h3><p id='' class='facts-text'>Purple is the official color of Congenital Diaphragmatic Hernia (CDH) Awareness. Show your support by wearing purple on CDH Action Day.</p></div></div><div id='' class='facts-item'><div id='' class='facts-header'><h3 id='' class='facts-number'>2</h3></div><div id='' class='facts-text-wrapper'><h3 id='' class='facts-title'>Host a fundraising event</h3><p id='' class='facts-text'>Organize a fundraising event to raise money for CDH research and support. This could be a bake sale, silent auction, or even a fun run/walk event.</p></div></div><div id='' class='facts-item'><div id='' class='facts-header'><h3 id='' class='facts-number'>3</h3></div><div id='' class='facts-text-wrapper'><h3 id='' class='facts-title'>Share your story</h3><p id='' class='facts-text'>Use social media or other platforms to share your personal experience with CDH and spread awareness about this condition. You never know who may be touched by your story and inspired to take action.</p></div></div><div id='' class='facts-item'><div id='' class='facts-header'><h3 id='' class='facts-number'>4</h3></div><div id='' class='facts-text-wrapper'><h3 id='' class='facts-title'>Educate others</h3><p id='' class='facts-text'>Take the time to educate others about CDH and its impact on families. This can be through a presentation at a local school or community group, or simply by sharing information with friends and family.</p></div></div><div id='' class='facts-item'><div id='' class='facts-header'><h3 id='' class='facts-number'>5</h3></div><div id='' class='facts-text-wrapper'><h3 id='' class='facts-title'>Support a CDH organization</h3><p id='' class='facts-text'>Donate or volunteer with a reputable CDH organization. Your support can make a difference in the lives of families affected by this condition.</p></div></div>
<div id='' class='whywelove-item'><div id='' class='whywelove-letter-cont'><div class='whywelove-letter'>A</div></div><div id='why-we-love-main-cont'><h3 id='' class='whywelove-title'>Raise awareness for a rare condition</h3><p id='' class='whywelove-text'>Congenital Diaphragmatic Hernia (CDH) is a birth defect that affects around 1 in every 2,500 babies. By having an Action Day dedicated to it, we can bring attention to this lesser-known condition and educate others about its causes and impact on families.</p></div></div><div id='' class='whywelove-item'><div id='' class='whywelove-letter-cont'><div class='whywelove-letter'>B</div></div><div id='why-we-love-main-cont'><h3 id='' class='whywelove-title'>Support affected families and individuals</h3><p id='' class='whywelove-text'>CDH Action Day provides a platform for families and individuals affected by CDH to come together, find support and share their stories. It's also an opportunity for the community to offer resources and assistance to those in need.</p></div></div><div id='' class='whywelove-item'><div id='' class='whywelove-letter-cont'><div class='whywelove-letter'>C</div></div><div id='why-we-love-main-cont'><h3 id='' class='whywelove-title'>Advocate for research and funding</h3><p id='' class='whywelove-text'>CDH Action Day also serves as a call to action for increased research and funding towards finding new treatments and potential cures for CDH. With more attention towards this condition, we can hope for better outcomes for affected individuals and their families.</p></div></div>
<div class='facts-overview'><div class='facts-item'><div class='facts-number-wrapper'><p class='facts-number'>1</p></div><div class='facts-core-content'><h3 class='facts-title'>Diaphragmatic Hernia is a Birth Defect Present from Early Pregnancy</h3><p class='facts-content'>This condition develops when the diaphragm, a muscle that separates the chest and abdominal cavity, fails to fully form during a fetus's development in the womb, allowing abdominal organs to move into the chest.</p></div></div><div class='facts-item'><div class='facts-number-wrapper'><p class='facts-number'>2</p></div><div class='facts-core-content'><h3 class='facts-title'>Surgery Soon After Birth is Typically Required for Survival</h3><p class='facts-content'>Infants born with Congenital Diaphragmatic Hernia usually require surgery shortly after birth to move the displaced organs back to their correct location and repair the hole in the diaphragm.</p></div></div><div class='facts-item'><div class='facts-number-wrapper'><p class='facts-number'>3</p></div><div class='facts-core-content'><h3 class='facts-title'>There are Two Main Types of Congenital Diaphragmatic Hernia</h3><p class='facts-content'>These are named for the location of the diaphragm opening: Bochdalek (most common, occurring on the left side) and Morgagni (rare, usually on the right side near the heart).</p></div></div><div class='facts-item'><div class='facts-number-wrapper'><p class='facts-number'>4</p></div><div class='facts-core-content'><h3 class='facts-title'>It is Often Detected during Prenatal Ultrasounds</h3><p class='facts-content'>A prenatal ultrasound can often pick up signs of this condition, such as abnormal positioning of the baby’s organs, providing vital early detection that can allow doctors to plan a strategy for treatment after birth.</p></div></div><div class='facts-item'><div class='facts-number-wrapper'><p class='facts-number'>5</p></div><div class='facts-core-content'><h3 class='facts-title'>Long-Term Prognosis Can Vary Widely</h3><p class='facts-content'>With advances in neonatal medicine, the survival rate for infants born with CDH is about 70%. However, long-term prognosis can vary depending on the severity of the condition and related health complications.</p></div></div></div>
Congenital Diaphragmatic Hernia Action Day is celebrated on April 19th every year. In 2024, it will fall on a Friday.
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