Thank you for visiting Team Missy Ann's page to show support for Missy, Brandon, Katie, and Rachel!
Team Details
- TEAM EVENT: June 13th at Saucy's in High Ridge Dine Out and Donate https://www.facebook.com/events/426914080191430/
- We walk to show support for the Markus family and all of those that ALS has touched
- All are welcome to join our team even if you cannot join us at the event, you can join us virtually
- Please make sure to join the team to get all the team updates, you do not need to fundraise to be part of the team
- Team Missy Ann Merchandise can be purchased at: https://stores.inksoft.com/team_missy_ann/shop/home
- All website questions will need to be directed to the walk contact at bottom of page
- If you have a fundraising idea, please email Jenny at jmduggan1717@gmail.com
If you would like to help in reaching our fundraising goal, you can make a personal donation or share your page and ask others to donate! Together we can make a difference in the lives of those affected by ALS. 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 a cure. Please consider joining our team in the Walk to Defeat ALS® or choose a team member from the list and donate to our cause.
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 disease. ALS occurs throughout the world with no racial, ethnic, or socioeconomic boundaries.
That’s why we’re participating in the Walk to Defeat ALS. To bring hope. To raise awareness. To provide resources and services to families free of charge. To help unlock the mystery of ALS and find the key to treatments a cure. Will you join us?
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!