Dear family & friends,
Today, October 3, is the 1 year anniversary of Wayne's passing. He lost his eleven year battle with ALS, but his memory and fighting spirit live on through the "Wayne Fuller Award"! Last year Kim accepted this new award started by the DC ALS chapter for the team that raises the most money! We will be walking in memory of Wayne this year and honoring the life that he so enjoyed and lived to the fullest everyday! All of the money raised stays in the DC area for families like the Fullers.
Please consider sponsoring us. With your help, we will be able to make a difference in the lives of people affected by this disease.
Thank you,
Jackie, Tim, Amanda, Kathryn & Rachel
Why We Need Your Help
Often referred to as Lou Gehrig's Disease, amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of an ALS patient averages 2 to 5 years from the time of diagnosis. Wayne is in 7+ years of fighting this disease.
Every 90 minutes a person in this country is diagnosed with ALS and every 90 minutes another person will lose their battle against this disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.
This crippling disease can strike anyone. Presently there is no known cause of the disease though support is bringing researchers closer to an answer. In the mean time it costs an average of $200,000 a year to provide the care ALS patients need. Help make a difference and donate or join a walk today.
