Larvinator's - 2024 is our 13th year as a team! As a team we have raised over $350,000 to help make a difference in the lives of those fighting. ALS provides so much not only to the fighter but to the fighters family.

Please continue to walk with us to raise awareness and much needed funds to support those still fighting ALS and their families. We are forever grateful for your help and support!

 We still fight, we still walk, and we carry on in memory of those we have lost and in support of those still fighting. 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 eventual a cure. We thank you for helping us reach our fund raising goal whether you have supported us in our previous efforts or if this is your first contribution. Together, we have no doubt we can make a difference in the lives of those affected by Lou Gehrig’s Disease.

As much as we appreciate the awards we have earned in previous years, we are walking because we can! In loving support and blessed memories! Almost everyone on our team has been impacted by ALS (through the loss of a family member or our dear friends, Larry and Russ) but we want to bring even more awareness. Whether you donate here or join our team and start your own fundraising! PLEASE make a difference! We are doing our best to do so!

 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 fatal disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.

ABOUT ALS

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!