Wellington North residents join Canadians in annual Walk for ALS

Wellington North residents joined people from across Canada on June 8 for the annual Walk for ALS.

More than 94 communities took part in the event for fitness, fun and the fight against ALS.

Every dollar raised goes to provide equipment, support services, education for the ALS community, and fund research to find a cure.

Locally, the event began at the  Arthur Pavilion and Ball Diamonds as participants prepared for the five kilometre walk.

In 2012, the Canada-wide event raised more than $3.2 million and in Ontario alone, $1.4 million was raised.

Amyotrophic Lateral Sclerosis (ALS) also commonly known as Lou Gehrig’s Disease, is a rapidly progressive and ultimately fatal neuromuscular disorder that causes the degeneration of a select group of nerve cells in the brain and spinal cord. As the nerve cells die, people with ALS lose control of their muscles, which makes breathing, eating, even smiling almost impossible.

Those afflicted have a prognosis of two – five years of life.

ALS attacks and kills the motor neurons in the body, denying the individual the ability to move, to speak and finally to breathe.

It has no known cause, no effective treatment and no cure.

ALS Canada provides equipment and support services for clients in Ontario, and funds breakthrough research towards a  cure. Approximately 3,000 Canadians live with ALS and two to three Canadians die of ALS each day. ALS can strike anyone, regardless of age, sex or ethnic origin The usual age of onset is between 55 and 65 , but some individuals are diagnosed before the age of 20.

Nearly 80 per cent of people with ALS die within five years of diagnosis. While some live longer, others die within a few months

ALS is a costly disease that affects patients and their families – emotionally, physically, and financially.

Donna Wright, of the Wellington North walk explained that this is the fourth annual event for Wellington North.

“The event is to raise awareness about ALS.”

She added there is plenty of information provided at the event for people to learn more.

“The money raised goes towards client services as well a research to find a cure.”

She added, “At present, there is little known as to causes and no known cure or treatment at this time.”

She noted the number of volunteers out so early in the morning, Wright said, “We have a really solid volunteer crew here.” In recent years, the event averaged between 140 to 200 participants.

The Arthur event included a penny table. Money raised from that also contributed to the walk proceeds. Those items were donated by local businesses and individuals within the community.

There is 1 comment.

  1. I have been suffering from amyotrophic laterals sclerosis (ALS) disease for the last three years and had constant pain, especially in my knees.I was tripping and unable to get upstairs due to (ALS), My doctor put me on riluzole, letting me know there was no cure but the medication might provide me a few more months of delayed symptoms.The Rilutek (riluzole) did very little to help me. The medical team did even less. My decline was rapid and devastating. The psychological support from the medical centre was non-existent and if it were not for the sensitive care and attention of my primary physician, I would have died. There has been little if any progress in finding a cure. With the help of Organic Clinic natural herbs I have been able to reverse my symptoms using herbs, which i feel has made the most difference. The ALS natural formula immensely helped my condition, it reversed my ALS. my slurred speech. And then the inability to eat without getting choked, and the Pains. gradually disappeared. Visit Organic Herbal Clinic via their official web-site www. organicherbalclinic. com. I’m now playing golf again. and i turned 68 today. DON’T GIVE UP HOPE!!

Comments