William is the son of Cecil Leach and Desiree Fry. William was born on June 14th 2018. At that time, he seemed to be what we believed, a normal healthy little boy. A few months after his birth, concerns began to arise that things were not the “norm”. In October, William was diagnosed with a extremely rare neurological disease known as Congenital Bilateral Perisylvian Polymicrogyria, also known as PMG. PMG is a disorder of the cerebral cortex (outer surface of the brain). In essence, a normal cerebral cortex of the brain consists of several deep folds and grooves. William’s consist of an increased number of folds that are very small. William’s is bilateral, which means both sides, which makes it even more rare. William had surgery about 3 months ago to have a feeding G-Button device, which allows his feedings to be done by a tube/line that inserts into the G-Button which goes directly into his stomach. He has recently been diagnosed with Cerebral Palsy as well as neuro and cardiac issues, which have resulted in numerous trips by Ambulance, Star Flight and vehicle to Dell Children’s in Austin and Texas Children’s in Houston. Seizures have became a part of his life the last 6 weeks. Expenses continue to mount every day. Please come out and support this amazing child and his family. Fried Catfish Dinner, by donation, Live Music by Southern Underground, Live Auction, Silent Auction and Baked Goods. A community comes together to support one another when one is in need. Please share! LLANO they NEED US.

July 13th, 2019 6:00 PM   through   10:00 PM
2249 RR 152
Llano, TX 78643
United States
Phone: 325-247-5354
Email: