WHY I WALK

Three years ago, my husband Lou was diagnosed with ALS. It is a horrible disease. Lou no longer has the ability to walk, he now uses voice control for his computer since his hands can not function and his whole body has weakened. This is a horrible disease and we are thankful that his progression has been slow. But it is not that way for everyone and no promises it will continue that way for 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, and presently there is no known cause or cure. 

A person with ALS becomes physically locked-in as the disease progressively paralyzes the body. The key to UNLOCK ALS begins with us. 

The past few 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. We can't stop now! It is only together that we will defeat ALS!  

I appreciate you helping me reach my Walk to Defeat ALS® fundraising goal! The Walk to Defeat ALS® is very important to me, as it raises funds to support those affected by ALS and to spread awareness of the urgency to find effective treatments and cures. 

Please consider walking with me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease. Click or tap on VIEW MY TEAM above to join, or on DONATE to make a donation.