We first noticed symptoms exactly 20 years ago with my husband, Dave LaRue. It’s hard to believe it was so long ago and yet seems like yesterday. His progression was fast and he died October 8, 2010.  The Rocky Mountain chapter of ALS United was a major support for our whole family during and after his illness. 

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, and presently there is no known cause or cure.

That’s why I’m walking. To change the statistics. To bring help and hope to those living with the disease. To ensure that no one ever hears the words: “You Have ALS” again.

The past two years have brought incredible advancements in ALS research, expanded access to care for people living with ALS, and enabled legislation that impacts the quality of life of people with ALS and their families.

But, we can’t stop now. The key to a cure begins with you.

Please consider sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease.

Thank YOU! Sending you peace, hugs, and good vibes!

Lisa LaRue & family