Jodi Larson was a mother, a wife, a sister, an aunt, friend, classmate, coworker; she was so many things to so many people. One thing that she was a fighter of ALS. Jodi was diagnosed in August 2016. The next chapter was full of unknowns. From learning how to navigate this new life, the ALS Association was there to help her and Dave (husband). After battling ALS for more than a year, Jodi passed away on January 27, 2018.
we invite you to help us celebrate jodi's life and unite to defeat als.
WHY WE NEED YOUR HELP
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.
That’s why we’re participating in the Walk to Defeat ALS. To bring hope. To raise awareness. To provide resources and services to families free of charge. To help unlock the mystery of ALS and find the key to treatments a cure. Will you join us?
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.
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!