Killian Family Celebrates 20 Years of Sam’s Night Fundraiser

The annual Sam’s Night event, hosted by the Killian family in Rockwall, Texas, marked its 20th anniversary on October 16, 2025, raising an impressive $1.5 million for Parent Project Muscular Dystrophy (PPMD). This event is the largest fundraising effort in the United States dedicated to advancing care, research, and advocacy for individuals living with Duchenne and Becker muscular dystrophy. Since its inception, Sam’s Night has raised over $10 million to support crucial advancements in treatment and care standards.

Two Decades of Community Impact

What began as a local family fair, known as Sam’s Family Fun Day, has evolved into a significant fundraising event that embodies the spirit and resilience of the Duchenne community. The event took place at Victory Social, where supporters gathered to celebrate two decades of progress in the fight against Duchenne. According to Pat Furlong, the Founding President of PPMD, “Sam’s Night is a testament to what families can achieve when they come together with determination and love.” She highlighted the remarkable journey from a time when families faced despair to the current era of hope fueled by research and advocacy.

The Killian family’s commitment to this cause reflects the strides made over the years, as children diagnosed with Duchenne now have improved life expectancy and quality of life due to advancements driven by community efforts like Sam’s Night. “Growing up with Duchenne has had many challenges, but Sam’s Night has always been a reminder that we are not alone,” said Sam Killian, whose personal journey has paralleled the event’s growth. “I’ve grown up alongside this event, and I’m proud that together we’re helping change what it means to live with Duchenne.”

Corporate Support and Future Goals

Numerous corporations supported this year’s Sam’s Night, including Altus Group, CBRE, and Wells Fargo, among others. Their contributions demonstrate the collective effort required to combat Duchenne. The event has transformed from a casual gathering into a sophisticated evening of connection and purpose, yet its core mission remains unchanged: to provide every individual living with Duchenne the best chance at a brighter future.

As the Killian family looks ahead, the focus remains on continuing to raise awareness and funds for Duchenne research and support. Individuals interested in contributing to this vital cause can still make donations by visiting SamsNight.org. PPMD continues to advocate for optimal care standards and innovative treatments, striving to ensure that families affected by Duchenne have access to the resources they need.

Duchenne muscular dystrophy is a genetic disorder that progressively weakens muscle strength, and PPMD is dedicated to fighting every battle necessary to end this disease. Since its establishment in 1994, PPMD has secured significant funding and facilitated numerous FDA approvals, all aimed at improving the lives of those affected by Duchenne. The organization remains resolute in its mission: to provide hope and a better future for all individuals living with this condition.