On a personal note...my family and I were devastated when this AWFUL disease took our mom/wife/grandma/friend away from all of us. It is so unfair that we cannot share anymore memories with my mom, and that she never saw Leah reach 2 years of age. I think about my mom every single day, and wish there was something I could've done. Now, it is too late for our family, but you never know if/when you will be affected by this terrible disease. It is random, sudden, and happens too quickly. There is not enough research to find a cure...yet. With your donation (of ANY amount) you will help get us one step closer to finding a cure and helping families who are suffering like we have. Thank you SO much for the support!!
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 yet it still costs loved ones 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.
