Top Tweets for #CHDS
Congenital heart diseases (#CHDs) are the most common type of major structural birth defects, affecting 0.86% to 1.0% of all live births. The diagnosis of CHD is usually made prenatally based on routine anatomy ultrasonography performed between 18 and 22 weeks of #pregnancy; however, CHDs are occasionally diagnosed postnatally.
Approximately 80% of all cyanotic #congenital #heart #diseases are caused by tetralogy of Fallot (TOF), D-loop transposition of the great arteries (TGA), and congenital heart disease with single-ventricle circulation.
➡️ Learn more in this JAMA Review: https://t.co/mX3j0eGYxS
Congenital heart diseases (#CHDs) are the most common type of major structural birth defects, affecting 0.86% to 1.0% of all live births. The diagnosis of CHD is usually made prenatally based on routine anatomy ultrasonography performed between 18 and 22 weeks of #pregnancy; however, CHDs are occasionally diagnosed postnatally.
Approximately 80% of all cyanotic #congenital #heart #diseases are caused by tetralogy of Fallot (TOF), D-loop transposition of the great arteries (TGA), and congenital heart disease with single-ventricle circulation.
➡️ Learn more in this JAMA Review: https://t.co/v4HBmGNNbA
CHDS MA alumna Jennifer Pearsall joined the @JEMSCONNECT podcast to discuss her NPS thesis on post-traumatic growth in emergency managers — what makes it possible, and what gets in the way.
Worth a listen: https://t.co/MQUe0gBNdJ
#CHDS #EmergencyManagement
Last September, Atlanta-area @ChickfilA restaurants raised a record-breaking $195,000 for our Kids at Heart program—a support community for parents, caregivers and families of patients with #CHDs who are treated at Children's. Learn more: https://t.co/sbpw3sPybr.
The Children's Heart Foundation is proud to fund the @AmerAcadPeds Pediatric Cardiology Research Fellowship Award. The award represents a tremendous opportunity for junior faculty in #pediatriccardiology to gain research experience. https://t.co/YiyAX8OeqF
#CHDresearch #CHDs
May is #MentalHealthAwarenessMonth. ❤ Children born with congenital heart defects face challenges that evolve over time. Beyond health and medical issues, many people living with #CHDs may experience psychological and social challenges from infancy through adulthood.
Today is #NationalSiblingsDay ❤️ Siblings share a special bond—and for those with a #HeartWarrior in the family, understanding #CHDs is an important part of that connection. Check out this video from our friends at the American Heart Association https://t.co/T6QBtbo14g
Today is World Birth Defects Day ❤️ Congenital heart defects (#CHDs) are the most common, affecting about 40,000 babies in the U.S. each year. At The Children's Heart Foundation, we fund research to help those born with CHDs live longer, healthier lives.
The Children's Heart Center is headed #Cardiology2025. Dr. Subhadra Shashidharan, Associate Chief of Cardiothoracic Surgery, is presenting research aimed at improving the lives of children with #CHDs. Learn more: https://t.co/My42GlW8rl.
The @American_Heart and The Children's Heart Foundation are investing in congenital heart defect research with $570,000 in new grants. Five researchers will advance their work to better understand and treat #CHDs. ❤️ Learn about the funded research here: https://t.co/UGyeksYxBd
Last September, Atlanta-area @ChickfilA restaurants raised a record-breaking $150,000 for our Kids at Heart program—a support community for parents, caregivers and families of patients with #CHDs who are treated at Children's. Learn more: https://t.co/sbpw3sPybr.
It's #NationalWearRedDay! ❤️ Show your support for all those impacted by congenital heart defects (#CHDs) by wearing RED today!
January is #BirthDefectsAwarenessMonth. Did you know congenital heart defects (#CHDs) are the most common birth defect, impacting nearly 1 in 110 babies? ❤️ We're funding research to improve diagnosis, treatment, and prevention. Together, we bring hope. 💕 #CHDAwareness
Every 15 minutes, a baby is born with a congenital heart defect. That means today, on #GivingTuesday, 96 new babies will face #CHDs. Despite being the most common birth defect, CHD research is underfunded. Help us change that! Make a difference today: https://t.co/8lwFjpZrDh
´Se te yon bèl moman inoubliyab #24 Mas 2024, yon bèl Konferans ki te baze sou #Ekosistèm pou devlope espò an Ayiti. Kite òganize pa ekip #CHDS la @NathanLaguerre1, kote @ralphganthier t ap pataje nan sa li konnen, e ki sa nou dwe fè pou devlope #Espò a isi.
Because of research, more babies with #CHDs are living into adulthood. But to ensure they live long, healthy lives, we need YOU. Join us for the country's premier walk series dedicated to funding congenital heart defect research. https://t.co/BrQhFtv9sW
Our new protocol is out:
First step in research supporting neurodevelopment delays for Infant Neonatal Intensive Care Graduates & infants at risk for Cerebral Palsy #CHDs #Prematurity
Thanks @Kelsie_Boulton @NadiaBadawiCPA @NovakIona & @CPAllianceAU
https://t.co/QqfRsrKilo
Day four of the #CHDS saw Dr Anne Alexander (CDH Learning Director) deliver a workshop on visualising cultural heritage data. A hands-on collaborative exercise, based on John Snow's map of cholera outbreaks in C19 London, enabled participants to flex their visualisation skills.
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