March 14, 2015 12:00 – 3:00 p.m. Ski as many laps as you can to raise money for ALS!
Carl Johnson, a close friend to Great Glen Trails and a lover of all things skiing, passed away in 2006 of ALS. This event is held in his honor, and in his spirit, it’s all about fun!
Get your family and friends to pledge money based on how many laps of the 5-kilometer course you will ski. It’s a ski-a-thon. Fundraising online! Click HERE to create your own fund raising page that you can share to your friends and family OR to donate to one of the competitors who already has a fundraising page. Watch the thermometer grow on behalf of Carl Johnson. It’s easy and fun!
Entry fee: $20, includes trail pass with all proceeds donated to the ALS Association. *All racers are encouraged to raise additional funds to help support the ALS Association. Prizes awarded for the most laps completed and highest amount pledged. As always, the event will feature a prize for the loudest & wackiest tights! The event will also feature an ALS benefit raffle for a handcrafted, wooden vessel made by Great Glen Trails Ambassador Ed Good and 2014 Olympic Biathlete Sean Doherty. Tickets are 3 for $5.
Day of Registration: 9:00AM-11:00AM
Amyotrophic lateral sclerosis (ALS), often referred to as Lou Gehrig’s disease, is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. The progressive degeneration of the motor neurons in ALS eventually leads to their death. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, patients in the later stages of the disease may become totally paralyzed. Yet, through it all, for the vast majority of people, their minds remain unaffected. There are currently no treatments that fully reverse the affects of ALS nor is there a cure.
THE ALS ASSOCIATION
The ALS Association is the only non-profit organization fighting Lou Gehrig’s Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure. Learn more about the ALS Association at www.alsanne.org.