This weekend, hundreds will lace up their shoes, not just to walk, but to bring hope closer for those living with amyotrophic lateral sclerosis. Each step taken will raise awareness and funds for ALS research, turning a morning walk into a movement of hope and determination.
Uniting friends, family and survivors in a powerful show of support to fundraise and spread advocacy for medical research, the Community Service club will hold its fifth annual ALS Walk this Saturday, Oct. 25 from 8 to 11:30 a.m. at the LHS track. Partnering with the ALS Association, this walk honorably raises money for patients of ALS, also know as Lou Gherig’s disease, to provide greater support for the needs of those battling this illness.
ALS & the ALS Association
ALS is a disease that affects a person’s brain and muscle movements, eventually taking away their ability to walk, communicate, eat, breathe, and overall, function on their own. The average life expectancy is 2 to 5 years. Currently, there are only treatments that can slow down the disease’s progression and there is also assistive technology to help serve those struggling. The ALS Association dedicates themselves to collaborating with clinics across the country to provide ALS treatment and make this condition livable until a cure can be found (ALS.org).
Showing up matters
On estimate, there are around 100 people living with ALS, just in New Hampshire. By just showing up, students and others who attend will support this cause and help the association get closer to finding a cure for ALS.
There is no admission fee to participate in the walk, but cash donations are greatly appreciated, as they go towards funding care. Community Service club hopes to see you there.
