There's no place like home for Erin
$12,160 raised
41% of $30k goal
61 contributors
4 Years running

It’s not often that someone is relieved to get a diagnosis that results in losing most of their muscle control.

But for Erin Kreiter, finding out that she has myasthenia gravis was better than always being told that her illness was an attention-seeking ploy.

Even if you don’t know Latin, the word “gravis” would set off warning bells. Indeed, there is no cure for “grave muscle weakness.” A chronic autoimmune neuromuscular disease that’s a cousin to muscular dystrophy, myasthenia gravis means that the message from nerve to muscle doesn’t get through.

In hospital

Today, the 29-year-old PhD candidate requires 24-hour care. If her ventilator — the machine that does the job her muscles in her diaphragm can no longer do — fails, she could breath on her own for only a minute. Her eyes are slightly droopy because keeping your eyes open requires muscle too. She can move her fingers and wrists, and wiggle her toes, but that’s about it.

Erin has had a lot to cope with since she walked into a hospital in August of 2012 and came home to Langley in an electric wheelchair and on a ventilator 360 days later. But instead of concentrating on what she can’t do, she focuses on what she can do. And top of that list is being able to live at home with her mom Janet, who works at the Trinity Western University Library, and her dad Tim, an RCMP officer who’s on leave until they can ensure they have round-the-clock caregivers seven days a week.

“It’s great, it’s crazy, it’s scary, it’s wonderful, it’s all of those things,” she says of what it’s like to be at home. In healthcare facilities, she spent a lot of time waiting for staff to help her. At home, the round-the-clock help from a caregiver means “I can go out and have a life. I can get back to my studies in September. I can have my friends over, go out to the movies or go out for dinner. I can take my puppy for a walk.

Sheldon and Me

“[The hospital] is a life of waiting and spending a lot of time alone in your room. I couldn’t imagine doing it for the next 50 years. I did it for a year and that was enough.”

It’s not without cost, however. The entire house had to be retrofitted to create a main-floor bedroom and accessible bathroom. The sunken living room floor was raised, walls were removed to make room for her wheelchair’s furniture-wreaking movements, doorways were widened, a wheelchair ramp was installed.

First birthday at home!

Friends and family helped out by lending them money and the Kreiters took out a second mortgage to pay roughly $200,000 in bills. This campaign is to help relieve that financial and emotional burden so they can move on to helping Erin realize her dreams.

“We’re getting it figured out,” says Janet. “We’ve come a long way. It’s a huge amount of work but once you get it figured out….”

“It’s the new normal,” Erin adds. Her mother nods her head. “You just do it.”


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