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Austin’s “Afternoon in NYC” Luncheon Raises $90K for Duchenne Research

The CureDuchenne Ladies Luncheon at Austin Country Club blends fashion and philanthropy, bringing the community together to support life-changing research for Duchenne muscular dystrophy

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(Standing left to right) Meredith Hannon, Jamie Bockius, Nancy Argent , Melissa Nelson (Seated left to right) Jenny Cokins, Marisa Phillips, Cassie Ford, Suzy Aubert

In a show of compassion and community spirit, the Austin community gathered on Sept. 26 for the annual CureDuchenne Ladies Luncheon, themed “Afternoon in NYC.” Held at the Austin Country Club, the event raised $90,000 for Duchenne muscular dystrophy research, supporting a cause that continues to impact families and inspire hope.

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Jamie Imber, Anu Reddy, Ali Watters

A family’s journey becomes a community’s mission

Duchenne muscular dystrophy, a rare genetic disorder affecting about 1 in 5,000 male births, gradually robs young boys of mobility and often claims their lives by their 20s. In Austin, however, a community is rallying to change that.

At the center of this effort are Tim and Laura Revell, whose two sons were diagnosed with Duchenne. Instead of succumbing to the devastating diagnosis, the Revells turned their determination into action, partnering with CureDuchenne and inspiring others to join their cause.

Over the years, the community has raised $6.2 million, funding crucial research and advancing new treatments. It stands as a powerful example of what can be accomplished when a community unites for a common goal.

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Venus Strawn, Tim and Laura Revell, Holly Mills-Gardner, Andrew Revell, Timothy Revell

Glamour for good

This year’s luncheon, hosted by Venus Strawn and Jennifer Stevens, brought a touch of New York City glamor to the Austin Country Club. While attendees sipped cosmos and previewed the latest fashion trends from The Domain, the event emphasized that style and substance can work together to make a difference.

Beyond the glitz, the stories of families like the Revells and the Sanfords resonated with the audience. Melanie Burton Sanford shared her family’s experience with gene therapy for her son Hudson at the CureDuchenne Clinic in Denton. While not a cure, the treatment marks a significant step forward in the fight against Duchenne muscular dystrophy, offering hope to families.

CureDuchenne’s progress over the past two decades has been notable. Since its founding in 2003, the organization has funded 18 research projects that have advanced to human clinical trials. By combining venture philanthropy with a commitment to patient care, CureDuchenne has accelerated the search for potential cures.

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Mary Ellen Patranella, Darryl Viernes Mineishi, Mandy Broussard & Jessica Rios

The path to a cure

The CureDuchenne Ladies Luncheon demonstrated that the generosity of the Austin community extends far beyond a single event. Each dollar raised and every bit of awareness spread brings the fight against Duchenne muscular dystrophy closer to victory for young boys and their families.

The battle against Duchenne is ongoing, but events like the luncheon show the strength of community, compassion, and hope. In Austin, participants aren’t just raising funds; they’re setting a new standard for what can be achieved when people unite for a common cause.

Looking ahead, the determination seen at the Austin Country Club in September will continue to fuel progress until a cure is found. And when that day comes, the community will have plenty to celebrate.

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