My Dear husband Jack was diagnosed with ALS (commonly known as Lou Gehrigs Disease in January 2019. It took over a year to try to figure out what was causing the weakness in his legs and arms. He went from walking our 2 Golden Retrievers 3 miles a day to not being able to walk anymore. There are currently no tests that can diagnose ALS, it's a disease of elimination of every other Motor Neuron Disease. The challenges are great, but with love and humor we are staying positive. Please come join us in our walk September 7th!
Our team is committed to raising money to support people in our community with ALS and spread awareness of the urgency to find treatments and a cure. Please consider joining our team in the Walk to Defeat ALS® or choose a team member from the list and donate to our cause.
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?
Amyotrophiclateral 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!