Global Alliance for Rheumatic and Congenital Hearts

A global movement for childhood-onset heart disease

We connect, empower and advocate to improve lifelong outcomes, by putting patients and families at the center.

World Congress, Hong Kong
UNGA 2026 side event, New York
Leaders' Forum
UNGA 2026 side event, New York
Patient voices

Stronger together

The largest global alliance of patient and family organizations for childhood-onset heart disease

Together, we are building a world where every child and adult living with congenital or rheumatic heart disease has access to the care and services they deserve.

90

Member organizations

53

Partner organizations

47

Countries

6

Continents

MemberPartner

Global Coalition

Global Coalition for Pediatric and Congenital Hearts

A joint initiative of Children's HeartLink and Global ARCH, uniting organizations around the world to make childhood-onset heart disease a global health priority, starting with a World Health Assembly resolution.

Global Coalition for Pediatric and Congenital Hearts. Secretariat work supported by Global Alliance for Rheumatic and Congenital Hearts and Children's HeartLink
Patient and family leaders on a Global ARCH Leaders' Forum video callEvery month on Zoom

For member organizations

Monthly Leaders' Forum

Our most important space to connect. Register once and receive every monthly invitation.

The patient and family voice

Nothing about us without us

Every Global ARCH member organization was started by people who live with heart disease or care for someone who does. Together, they make sure lived experience shapes every ask to governments and global health leaders.

Global ARCH at a United Nations panel on children and young people with NCDs

Our roots

Built by families, one gathering at a time

A mother and daughter at Hearts Together 2024
Group photo at a Heartfest transition event
Table discussions at Hearts Together
Climbing wall at a Heartfest transition event

Join the movement.

Join a worldwide community of patient and family organizations. Membership is free.

Amy Verstappen, Founder

Amy Verstappen has been a patient advocate and health educator since 1996, when her own challenges living with a complex heart defect led her to the Adult Congenital Heart Association, where she served as president from 2001 to 2013. She has served as an advisor to the Centers for Disease Control the National Heart, Lung and Blood Institute; and the International Society for Adult Congenital Cardiac Disease, and worked with congenital heart patient and professional groups throughout the USA and the world.  Ms. Verstappen received a Masters in Education in 1990 and a Masters in Global Health in 2019.