Help me raise money to find a cure for ALS!
Welcome to My Fundraising Page
|Date:||Saturday, September 24, 2022|
For the fifth year in a row, I am participating in the Vermont Walk to Defeat ALS in honor of my Grandma who passed away on February 10, 2018. My Grandma was my biggest supporter and fan in everything I did, no matter where I was. I am thankful I was able to spend her last 7 months of life living with her and caring for her each day. I hope you consider joining team CHB on our walk in September, or help donate to the cause.
Thank you for helping me reach my Walk to Defeat ALS® fundraising goal! This is an exciting opportunity for us to work together to support those affected by ALS and to spread awareness of the urgency to find treatments and a cure.
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. WE CAN'T STOP NOW!
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.
Why We Need Your Help
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.
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.
ALS can strike anyone. Presently there is no known cause of the disease, though support is bringing researchers closer to an answer. In the meantime it costs an average of $250,000 a year to provide the care people living with ALS and their families need. Join the movement to bring help and hope today!
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