My dad lived with ALS for 4 and a half years. During that time we did so much as a family and enjoyed everyday together. After he was diagnosed the ALS association was more than helpful for my family. My dad participated in one of the ALS clinics and he participated in 2 clinical trial. My dad also went to Washington D.C. to talk to his local congressmen and advocate for this disease. The quality of life my dad was able to have would not have been made possible without this organization. The money that we raise goes helps to fund these clinical trials that could one day cure ALS. Join me and my family in this fight against ALS.
Thank you for helping me reach my Walk to Defeat ALS(R) fundraising goal! This is an exciting opportunity for us to work together to support those affected by Lou Gehrig's Disease and to spread awareness of the urgency to find treatments and a cure.
Please consider walking with me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease. I encourage you get your friends, family, neighbors and coworkers involved!
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.
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.
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