Celebrate the Life of Jay Edwards
Dad's Birthday at The Price is Right!
On September 11, 2025 James (Jay) Edwards found eternal peace. My father endured ALS for four years; losing the ability to speak, then eat, then move. He rose above suffering with grace. His humor kept my spirits lifted and his humility filled me with strength. I encourage you to walk and/or donate to the JAYBIRD Team to honor my dad and others who are and have endured this illness.
Thank you for helping me reach my Walk ALS Greensboro fundraising goal! The Walk ALS Greensboro raises funds to support the ALS community in North Carolina and to build ALS awareness to find treatments and a cure.
Amyotrophic lateral sclerosis (ALS) is a progressive, fatal disease that slowly robs the body of its ability to walk, talk, swallow and breathe. The life expectancy of a person with ALS averages 2 to 5 years from the time of diagnosis. ALS can strike anyone, at any age and there is still no known cause or cure.
That's why I'm walking. To build a future without ALS. To bring help and hope to patients and families affected by this terrible disease, in the hopes that one day ALS is a disease of the past.
Over the past few years, there have been advancements in ALS research, as well as expanded resources and access to care for people living with ALS.
But now, more than ever, we need to keep the momentum going. We need to continue to push for more treatments and find a cure for ALS.
Please consider joining me at the walk - we will walk and roll together, united with wheelchairs and scooters, families, neighbors and friends, strollers and pets ? all are welcome! If you can't make it to the walk, please consider making a donation. With your support, we can make a difference in the lives of people affected by this disease right here in North Carolina.
