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The mission of the Down Syndrome Association for Families of Nebraska is to improve the lives of individuals with Down syndrome by empowering them as well as educating and supporting their families and the larger community.

News & Notes

I joined DSAF back in April of 2021, when I received a prenatal diagnosis of Trisomy 21 for my son, Henry ‘Hank’ Eugene Koon. After being advised to terminate by two different doctors simply because of his diagnosis, I was a pretty scared and desperate first-time mother-to-be.

We Need Your Help

DSAF aims to provide programs and events free of charge or at greatly reduced rates for our community. As costs continue to rise, we strive to maintain existing programs and grow to meet the needs of individuals with Down syndrome, their families, providers, educators, and employers. Please consider making a monthly contribution to help us continue to serve our members! 

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