Shady Strong originated in 2019 supporting a loved one with ALS. Since then, thousands of dollars have been raised through donations, fundraisers, and community support to help raise awareness, advocate, fund research, and support ALS families.
In 2022, Shady Strong became a federally recognized non-profit with a mission to raise money that will go directly to families battling ALS.
Our ALS Journey
Remembering Robert J. Shady: A Life Lived with Strength and Service
Robert J. Shady, affectionately known as Bob, faced the battle of his life when he was diagnosed with bulbar onset ALS in May 2018. Coming from a background of proud military service with the United States Army during the Vietnam era, Bob's unwavering spirit and commitment to others shone through, even in the face of this challenging diagnosis.
As the effects of ALS gradually impacted his speech and muscles, Bob sought support from the Syracuse Veteran's Association, marking the beginning of a vital support network that accompanied him throughout his journey. With the assistance of organizations like the Paralyzed Veterans of America, Bob strived to maintain his independence, displaying remarkable resilience in the face of increasing limitations imposed by the disease.
Despite the immense challenges he faced, Bob's faith remained unshakable, and his generous and selfless nature continued to touch the lives of those around him. Whether it was lending a helping hand to a friend or a stranger in need, Bob's enduring legacy of compassion and service inspired the birth of Shady Strong, a poignant testament to his unwavering spirit.
Today, the legacy of Robert J. Shady lives on, carried forward by Shady Strong, a symbol of his love for his family and friends, and his dedication to serving others. Though Bob may no longer be with us, his impact and the strength of his character continue to resonate, shaping the ongoing mission of Shady Strong as a beacon of hope and support for those affected by ALS.
