Thank you for helping us reach our fund raising goal! Together we can make a difference in the lives of those affected by ALS. Our team is committed to raising money to support people in our community with ALS and spread awareness of the urgency to find treatment and a cure.
For almost 5 years, we have watched this disease take over our world. Our young, once strong and healthy Solomon is fighting a brave and courageous fight for our entire family. Our boys can’t fully understand how and why their daddy can’t talk or play with them the same way as in the past have made life as “normal” as it could be during this time.
The statistics are stark and depressing. Despite years of research, the disease is so complex that it is variable in every patient, so attempts to find a cure are a way off yet.
Why We Need Your Help
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 a person with ALS 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.
ALS can strike anyone. Presently there is no known cause of the disease, yet it still costs loved ones an average of $250,000 a year to provide the care people living with ALS and their families need. Join the movement to provide help and hope today!