Register for a Walk Today!
Walk for 1 in 100, ACHA's brand new fundraising campaign, raises money for outreach, education, research and more.
9th Annual ACHA Conference Registration is Open!
Make plans today to join ACHA in Minnesota from Oct. 15-17, 2020. Our event offers the best in CHD education, plus plenty of social opportunities.
Announcing ACHA's Inaugural Research Grants
We are funding three provider research grants and three fellow research grants, focusing on crucial topics surrounding adult congenital heart disease.
ACHA's National Accreditation Program
More than 30 centers throughout the United States have earned ACHA Adult Congenital Heart Disease (ACHD) Accreditation.
Find your doctor
Connect with practices and practitioners specializing in adult congenital heart disease.
Clinic Directory
Living day-to-day
Living with a congenital heart defect requires critical attention to even the most ordinary medical procedures, like a dental visit.
What I need to know
NEWS & EVENTS FROM ACHA
October 14, 2019
ACHA to Recognize Evan Michael Zahn, MD, for Contributions to Congenital Interventional Cardiology
Heart to Heart Peer Support Program
CHD patients and their families can connect one-on-one with a trained peer mentor who can relate to their CHD experience.
LEARN MORE
Walk for 1 in 100
Raise vital funds for the 1 in 100 children and adults impacted by CHD across the country.
WALK WITH US
Corporate Matching Tool
Do you know if your employer will match your donations to ACHA? Our online tool makes it easy to find out!
FIND OUT NOWSupporting Patients
and Families
and Families
Congenital heart disease is survivable, manageable, yet in the routine years between infancy and adulthood, sometimes forgettable. The Adult Congenital Heart Association is a resource, advocate and knowledge base for everyone affected.
Find out more
Empowering
Providers
Providers
Treating congenital heart defects in adults is to understand the continuum of the disease from its infancy. The Adult Congenital Heart Association brings together valuable research, training opportunities and standards of care to help you help your patients and further define this specialization of cardiovascular disease.
Get started
By bringing our expertise on congenital heart disease to the adults that live with it, we offer the promise for safer, healthier lives.
A Blog for the Congenital Heart Disease Community
Pedaling the Pounds Off: Where My Sto…
Hello, world! My name is Jared Gould. I was born with hypoplastic left heart syndrome (HLHS), a congenital heart defect …
Medical Trauma: Guilt vs. Thankfulnes…
If you’ve had open heart surgery, you’ve been through medical trauma. I was born with the congenital heart defect tetral…
My Parents' Role in My Relationship W…
My fragility is something of a running joke in my family. The Easter after my aortic valve was replaced with a mechanica…
How Anxiety Helped Me with CHD
When I was in graduate school, I literally thought I was dying—having severe palpitations and waking up sweating and una…
Measuring the Immeasurable
It's been six months since I got my surprise gift, a brand new combination pacemaker and defibrillator. I learned severa…
The Very First Walk for 1 in 100
The inaugural Walk for 1 in 100 series kicked off this past Saturday at Wheaton Park in Maryland, and was nothing short …
From Camper to Counselor
Two weeks after I was born, the doctor came rushing in with more doctors behind him during my check-up to discover I had…
Why Show Up?
This year marked my third consecutive year going to Washington D.C. for the Congenital Heart Legislative Conference. To …
A Heart Month Message from the ACHA B…
Hello ACHA members, and Happy Heart Month!
I am the Immediate Past Chair of the ACHA Board of Directors, and I am also …
Walk for 1 in 100 Spotlight: Villains…
The Bearded Villains are a worldwide brotherhood of elite bearded men from all over the world who are dedicated to the b…