“The Young and the Restless” star Kate Linder (Esther Valentine) has once again teamed up with ALS Network to host a charity event benefitting ALS research and care, in honor of her late mother, Molly Wolveck.
Appearing on the CBS daytime drama series for more than 43 years, Linder became the celebrity spokesperson and ambassador for ALS and ALS Network in 2004, just as her late brother-in-law Scott Buzzell, was diagnosed with ALS, with Linder and her late husband, Dr. Ron Linder, as well as their families, including Molly, determined to do everything they could to find a cure.
Fundraising, raising awareness and lobbying Congress for ALS Network for more than two decades, Linder recognizes the dedication ALS Network has in finding treatments and cures for the insidious disease.
With her late mother’s dual commitments to both art and to finding a cure for ALS through the ALS Network, Linder will host a reception and art sale to celebrate her artwork on Sunday, August 17, from 2:00-5:00 p.m. PT at the 9176 Gallery, located at 9176 Sunset Blvd., West Hollywood, CA.
“I’m thrilled that my mom’s artwork will once again be able to help people with ALS through the ALS Network,” said Linder in a statement. “I’m looking forward to seeing everyone there for a wonderful afternoon filled with amazing art from my mom and from other artists so that we can make even more progress towards finding a cure for ALS.”
Wolveck passed away on June 1, 2023. She was 98 years old.
During last year’s fundraiser event, Linder donated even more of her mom’s artwork. Additionally, Craig Byrd and Roy Oldenkamp were inspired to donate artwork by other artists from their personal collections to help the worthy cause. The art will be on display and available for purchase with all of the proceeds going to the ALS Network.
To attend the event, submit RSVPs to TeamKateLinder.org. The gallery space is generously being donated by local Southern California developer Faring. All proceeds benefit ALS Network.
For more information about the event, check out the flyer below.
About ALS Network
Amyotrophic lateral sclerosis (ALS) is a fatal, neurodegenerative illness that affects nerve cells in the brain and the spinal cord. People with ALS lose the ability to move, speak, swallow, and, eventually, to breathe – all while their minds and senses usually continue to function. People who have served in any branch of the military are diagnosed with ALS nearly twice as often as the general population. Currently, there are no known cures for ALS and only modestly effective treatments. The mission of the ALS Network is to partner with the ALS community as we drive the discovery of prevention strategies, treatments, and cures for ALS; provide access to quality care and connection; and promote initiatives to improve health outcomes.
