Sudbury

'When I can't communicate, that's the time for me to check out,' memoir tells journalist's journey with MAID

Diane Sims, a journalist originally from Sault Ste. Marie, Ont., has a new memoir detailing her health struggles and considering medical assistance in dying as an option.

Diane Sims was diagnosed with multiple sclerosis when she was a teenager

An older woman with red hair sitting in a studio with a microphone in front of her.
Diane Sims has worked as a journalist for the Manitoulin Expositor, the CBC, and freelancing for multiple newspapers across Canada. Now she has a new memoir which covers her decision to pursue medical assistance in dying. (Markus Schwabe/CBC)
We spoke with northerner Diane Sims about her memoir called "Living Beyond the Shadow." In it, she talks about her struggle for decades with Multiple Sclerosis... and cancer... and her decision to pursue medical assistance in dying. 

Diane Sims has already written her own obituary.

The journalist, originally from Sault Ste. Marie, Ont., has been told she was going to die since she was first diagnosed with multiple sclerosis (MS) as a teenager.

That diagnosis didn't stop her from pursuing a career in journalism, working at the Manitoulin Expositor, which she calls the "best newspaper in the universe," in the 1980s, while also freelancing for other newspapers, including the Toronto Star, and contributing to the CBC.

Sims is now 66, and said the disease has taken its toll.

"I have been in a wheelchair for about 14 years," she said. "I have very little freedom. I can't do anything for myself."

In her new memoir, Living Beyond the Shadow, she writes about her decision to pursue medical assistance in dying (MAID).

It's a decision Sims said she made during the COVID-19 pandemic when a doctor, again, told her she didn't have long to live.

"I was told I had three months to live because I have a dying colon," Sims said.

Although that did not come to pass, Sims said she doesn't want to end up living in a long-term care home once her health deteriorates.

"We all saw what happened with COVID and I did not want to put Dennis [her husband] through making that decision to put me into a long-term care facility," she said.

If she can't function to do things she wants to do, I can understand where… basically that would be an alternative.- Dennis Thomas, Diane's husband

Sims refers to her voice as "monotone" because of her MS and said once she loses the ability to talk and use her hands, she'll pursue MAID.

"I'm a communicator, and when I can't communicate, that's the time for me to check out," she said.

Her husband, Dennis Thomas, said it was difficult when she first told him she was considering MAID.

"But then I understood what she was talking about," Thomas said.

"If she can't function to do things she wants to do, I can understand where… basically that would be an alternative."

Thomas added that if his wife's medications to manage her MS get much more expensive, MAID could become the only option available to her.

"If you look at the pharmaceutical companies, if they make a decision that they're going to make these drugs that she needs to survive so expensive, she can't afford to buy them," he said.

"What's the difference between that and MAID?"

Sims said she has some living left to do, though, before her condition and quality of life worsen.

With files from Markus Schwabe