Cure CrewLiving with Scleroderma

Dinking for a Difference: Picklepalooza 2024 Raises $23k for Scleroderma Research

By November 21, 2024No Comments

This year, Beth L. and Lisa D. brought the second annual Picklepalooza to life, hitting the courts for a cause close to their hearts.

Beth, a Cure Crew champion with more than two decades of scleroderma advocacy, has organized everything from golf tournaments to restaurant fundraisers since her mother mother’s diagnosis in 1997. “In memory of my mother, Betty, we continue to raise awareness as well as funds to find a cure for those who are living with scleroderma,” she says. Before losing her battle in 2009, she asked that we continue the fight because together, we can make a difference.

For Lisa, the fight is personal, too—her daughter’s diagnosis has fueled her dedication to supporting the Scleroderma Research Foundation.

“We are so grateful for the resources offered by the SRF,” Lisa says. “Raising money for this organization ensures our daughter, along with all those with the disease, gets the best support and research possible.  The hope of giving them a chance at a healthier future means the world to us.”

Hosted at the Austin Pickle Ranch, the tournament drew a lively crowd to watch the 52 participants compete for top prizes, score bragging rights, and enjoy an unforgettable day of friendly competition. Let’s hear it for Beth, Lisa, and the whole Picklepalooza team for their incredible efforts benefiting the search for a cure to scleroderma. 👏

Want to make a difference? Consider joining Cure Crew—a passionate group of supporters raising awareness and funds for scleroderma research.