Diane Jenson, is a member with the Prince George Walk for ALS and says the cause is one close to her heart.
ALS awareness

TYH: ‘It’s close to my heart,’ ALS Walk goes virtual this ALS Awareness Month

Jun 16, 2020 | 8:00 AM

For many the month of June may mark the beginning of summer, but for others June is the time to bring awareness to ALS.

ALS, a.k.a Lou Gehrig’s Disease is a progressive neurodegenerative illness, meaning that those affected gradually begin to lose their ability to control their muscle movement, and eventually succumb to the illness.

“My mother passed away from ALS in 2008.”—Diane Jenson, member, PG Walk for ALS

For local volunteer, Diane Jenson, the cause is close to her heart, her mother was diagnosed with ALS at the age of 70, and didn’t make it to her 74th birthday. “There is no cure, and the possibility of one is there,” says Jenson, “we can eliminate this disease, we just need to put a little bit of focus, awareness, and some cash into it and the cure will be found. I’m sure of it.”

ALS is usually diagnosed in adults age 55-75, once diagnosed there is a two to five year life expectancy.

“We are having online walks, virtual walks, all across Canada.”—Diane Jenson, member, PG Walk for ALS

Locally, a walk to raise awareness is usually held, however, due to the ongoing COVID-19 crisis, the walk is going virtual. People are encouraged to register online for the walk, and participate by donning purple, walking with friends and family (safely) and sharing photos online.

Jenson notes that those with ALS, are encouraged to reach out to the ALS Society of B.C. for support. The ice bucket challenge which was popular several years ago, helped the ALS Society allocate $15 million towards ALS research across Canada. According to the ALS Society there are 12 people living with the disease in northern B.C.