Lincoln Teen Received Dream Weekend Experience
An 18-year-old Lincoln resident received a surprise sendoff before a weekend of sports-themed events at UNL.
Updated on Oct. 10, 2026 in Special Needs
Dream on 3 selected 18-year-old Sam Schreiner for a special dream weekend in Lincoln. The experience kicked off with a community celebration before a tour of the Devaney Center.
Why it matters
Programs like these provide meaningful opportunities for local families managing significant health challenges. Sam Schreiner, who has Down Syndrome, diabetes, and kidney disease, was recommended for the initiative by the Down Syndrome Association for Families.
Sam Schreiner is an 18-year-old participant selected for this dream weekend experience. He was recommended for this recognition by the Down Syndrome Association for Families.
The players
Sam Schreiner
An 18-year-old Lincoln resident who was selected for a dream weekend experience.
Dream on 3
A non-profit organization that coordinates sports-themed dream experiences for children and young adults with life-altering conditions.
Down Syndrome Association for Families
A local support organization that advocates for individuals with Down Syndrome and provided the recommendation for this program.
The details
The weekend experience began with a home sendoff organized by Dream on 3, where family, friends, and neighbors gathered to celebrate. Following the sendoff, Schreiner traveled to the Devaney Center at the University of Nebraska-Lincoln via limousine for a private tour of the sports facilities.
Timeline
Friday, October 9, 2026: Sam Schreiner received a home sendoff.
Saturday, October 10, 2026: Sam Schreiner attends Huskers pre-game festivities.
The Home Front
This experience follows a pattern set by established youth wish-granting models that prioritize personal interests and community involvement. It highlights how local support networks collaborate with national programs to provide specialized experiences for families.
Families interested in support services should maintain contact with local advocacy groups like the Down Syndrome Association for Families. These organizations often serve as the primary link to regional and national programming opportunities.
The takeaway
Community-led events can create lasting memories for families navigating complex health needs. Keep a list of local advocacy organizations on file to stay informed about potential opportunities for your family members.
Further reading
For resources on support programs, visit Special Needs.
