Bea Coker
reporter2.riverbendnews@gmail.com
The Branford community is rallying behind Darbi Holtzclaw and her infant daughter, Lainey, as they navigate the challenges of a recent diagnosis. Lainey, just a few months old, has been diagnosed with a rare genetic mutation, THG1L, shedding light on the complexities of mitochondrial disorders. The diagnosis, attributed to homozygosity for the p.Val55Ala mutation in THG1L, has sparked a wave of support from neighbors, friends and local businesses. Researchers suggest that this mutation disrupts mitochondrial function, particularly affecting cellular response to glucose levels, often leading to autosomal-recessive cerebellar atrophy.
In response to the mounting medical bills associated with Lainey's care, J. W. Hill & Associates, Inc. is organizing a benefit auction. The auction aims to alleviate the financial burden on the Holtzclaw family and provide them with the necessary resources for Lainey's treatment. "We believe in the power of community support," remarked Virginia Yetton, who is assisting J. W. Hill & Associates, Inc. "It's heartwarming to see our town come together to help a family in need."
Residents are encouraged to contribute by donating items for the auction. Donations can be dropped off at the JW Hill and Associates office, located at 203 East Howard St., in Live Oak, or by calling (386) 362-3300 to schedule a drop off at the auction location. Additionally, Yetton will be available at the Catfish Festival in Branford on Saturday, April 13, to collect donations and offer support for the Holtzclaw family.
The benefit auction is scheduled for Saturday, March 23, at 9 a.m. It promises to be an evening of community solidarity and generosity as residents bid on items to support Lainey's ongoing medical care. For those unable to attend the auction, contributions can also be made directly to the Holtzclaw family's Capital City Bank account under the name Darbi Holtzclaw, which has been set up to aid in covering medical expenses. As Branford stands united behind the Holtzclaw family, the outpouring of support serves as a testament to the strength and compassion of this close-knit community. disrupts mitochondrial function, particularly affecting cellular response to glucose levels, often leading to autosomal-recessive cerebellar atrophy.