Thank you for helping me reach my Ride to Defeat ALS fundraising goal!
Every year I take this opportunity to ride in remembrence of my aunt Arlene. The memories were many as she was so full of life, however, her time was cut short by this terrible disease. It is my hope that through research we can help to abolish this disease in the near future.
Please consider supporting my efforts by giving a tax deductible donation towards my goal. I have reached my goal, so a$10 donation would be appreciated. Please know any amount helps and every dollar makes a difference.
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 a person of their ability to walk, speak, swallow and eventually breathe. The life expectancy of a person with ALS averages only 2 to 5 years from the time of diagnosis. In a very short period of time, the person and their family need a myriad of services and support The ALS Association is their one-stop-shop.
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.
The ALS Association Oregon and SW Washington Chapter supports families living with ALS at each and every stage of the disease. Through local monthly support groups, medical equipment loan closets, caregiver support, partnerships with multi-disciplinary clinics, and so much more - services are provided at no cost to the person with ALS and their family. The local chapter receives no government or insurance funding, but is supported through events like the Ride to Defeat ALS.
Prefer to make a donation by check? Click here for a printable donation form!
