This account is for the “Ella’s Cross” event being put on by Waylon Piercy. The event will be a 50 mile walk on September 6, 2025, carrying a wooden cross to honor Ella & all others with SMA.

This is Ella Jayne. She is 15 from West Monroe. Ella was born with a rare, genetic condition called Spinal Muscular Atrophy. It is a neuromuscular disease that affects her whole body.

The funds raised here will be donated directly to Ella’s medical fund to cover the future costs of medical travel & needs.

$5,000 is to be split between Ella’s medical account & CURE SMA. CURE SMA is a wonderful organization that supports families affected by SMA through care packages, conferences, and medical equipment. They do many things our community is grateful for.

We are very blessed by and appreciative of all your support