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West Kootenay WALK for ALS June 3

Contributor
By Contributor
May 17th, 2018

Lakeside Rotary Park will be the place to be Sunday, June 3 for The WALK for ALS.

Volunteers, families and friends are gathering once again to raise funds and awareness for people living with ALS.

The WALK for ALS is the ALS nationwide signature event to raise awareness and funds for patient services, and ALS research. It empowers people affected by ALS — the patients, families, friends, caregivers, and health professionals — to take back some of what ALS has taken away.

Among the 15 WALKs happening this year, the West Kootenay WALK will be held in Nelson, with registration set for 10 a.m. The WALK begins at 11 a.m.

Volunteers will also be organizing various activities for participants of all ages.

“The hard work of our volunteers and staff at ALS BC, along with the funds raised from the WALKs help to support people with ALS in BC tremendously,” says Wendy Toyer, Executive Director of the ALS Society of BC. “Through their efforts, we are able to provide crucial medical equipment, support and other services for people affected by this disease.”

Proceeds from the WALK for ALS go to the ALS Society of BC to provide support services for people living with ALS in BC, and to the Canadian ALS Research program to strive toward a world without ALS.

WALK with us to stop ALS in its tracks. Register today at www.walkforals.ca

About Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis (ALS) is a rapidly progressive, neuromuscular disease. It attacks the motor neurons that transmit electrical impulses from the brain to the voluntary muscles in the body. When they fail to receive messages, the muscles lose strength, atrophy and die. ALS can strike anyone at any time, regardless of age, gender, or ethnic origin. It does not affect the senses, and only rarely does it affect the mind.

About ALS Society of BC

The ALS Society of BC raises funds for research, and to provide direct support to ALS patients, and their families and caregivers. Until a cure is found, the Society provides patient services to improve the quality of life of those diagnosed with this disease by offering an extensive equipment loan program, support groups, and educational materials.

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