06/05/2026
The Down Syndrome Association of Wisconsin (DSAW) is aware of recent public discussions surrounding a prenatal diagnosis of Down syndrome and the decision a family made following that diagnosis.
DSAW respects that reproductive and medical decisions are deeply personal. Families facing a prenatal diagnosis deserve compassion, support, and the freedom to make decisions based on their own circumstances and values.
At the same time, we are concerned when public conversations about Down syndrome include inaccurate, outdated, or incomplete information that can perpetuate fear and misunderstanding about what it means to live with Down syndrome today.
A diagnosis of Down syndrome is not a prediction of a person's worth, potential, happiness, or quality of life. While individuals with Down syndrome may experience health, developmental, or educational challenges, outcomes vary widely and continue to improve as a result of advances in healthcare, education, employment opportunities, and community inclusion.
People with Down syndrome are students, employees, artists, athletes, advocates, friends, neighbors, volunteers, and valued members of their communities. They build relationships, contribute to the workforce, pursue personal goals, and enrich the lives of those around them. To portray a Down syndrome diagnosis as a life defined primarily by suffering, limitation, or burden does not reflect the experiences of many individuals and families living that reality every day.
Research consistently demonstrates that individuals with Down syndrome and their families report high levels of happiness, meaningful relationships, and life satisfaction. While challenges exist—as they do in every family—those challenges are only one part of a much larger story.
When public figures share their experiences, their voices carry influence. For that reason, it is especially important that discussions about Down syndrome are grounded in current, evidence-based information and include the perspectives of people with Down syndrome themselves. Families deserve access to balanced information that reflects both potential challenges and the many possibilities available to individuals with Down syndrome in today's world.
For more than 35 years, DSAW has served individuals with Down syndrome and other developmental disabilities and their families across Wisconsin. Every day, we witness people with Down syndrome learning, working, contributing, leading, forming meaningful relationships, and living full lives in communities throughout our state.
Every family deserves the opportunity to make decisions informed by accurate information, current medical understanding, and the voices of people with Down syndrome themselves.
For families who have recently received a prenatal or postnatal diagnosis, DSAW's Parent's First Call program offers confidential peer support, current information, and connections to other families who are living the experience. Our goal is not to tell families what decisions to make, but to ensure they have access to accurate information, meaningful support, and authentic perspectives from individuals with Down syndrome and their families.
To learn more about Parent's First Call, contact (414) 327-3729 option 3, email [email protected] or visit https://www.dsaw.org/support/expecting-parents/.
The voices and lives of people with Down syndrome matter. Their stories deserve to be told fully, accurately, and with dignity.