Thank you for helping me reach my Walk to Defeat ALS® fundraising goal! This year I will be walking in memory of my brother Mike.  Undoubtably the best big brother a girl could have growing up, he was one of the kindest and most gentle people that ever walked the Earth and I will forever miss him.  This horrible disease stole my brother from his family in one of the worst ways.

The past two years have brought incredible advancements in ALS research, expanded access to care for ALS patients, and enabled legislation that impacts the quality of life of patients and their families. WE CAN'T STOP NOW!

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. 

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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