My personal walk for ALS
Many of you know, I lost my husband Chuck Molt to ALS (Lou Gehrig’s Disease) on October 31, 2020. There is no cure for ALS and no effective treatment options. I am participating in The Walk to Defeat ALS to help raise awareness of the urgency to find treatments and a cure and to make it so no family has to go through this.
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. Chuck only had 2 months! 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 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.
Raised the amount of money defined for this milestone
I Made a Difference!
I supported this event with a personal donation.
Fundraising Honor Roll
Lynne and dave
Pat Molt - Chuck's Chicks
The Osani Family
John & Curly
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