Uncertainty in an uncertain world
Guest post by: Danielle D’Annunzio I never thought I would have to worry about the challenges that a chronic neurological disease could suddenly…
Lessons From Cyber School: A First-Year Teacher During COVID-19
Most teachers remember their first year in the classroom. For Spencer Davis, a first-year teacher who was diagnosed with MS last year, the…
A Fruitful Partnership
Every partnership has a story. For some, it starts with a vested interest in helping communities in need of support. For others, it’s…
Step by step: the Return to Running
Guest post by Lori Kemp For Lori Kemp, running has always been connected to multiple sclerosis (MS). It was a probable MS diagnosis…
Inhale, exhale: Healing through mindfulness
Guest post by: Sarah Bily My mother was diagnosed with progressive MS when she was only 34 years old. At the time, I…
Uphill Battles
For Charlotte Ward, an agrologist in Saskatchewan, summer is her busy season. Her family resides on a farm near Springside, centrally located near…
Behind the PPE: Caring in a Crisis
“It’s not easy to be young and require institutional care.” Nicole Nadeau-Fréchette is a social worker at a long-term care facility in Winnipeg,…
Q&A: Caregiving during COVID-19
During the rapidly evolving COVID-19 pandemic, loved ones are stepping up to care for and protect the safety of vulnerable populations. For those…
Selfishness as a revolutionary act of kindness: How to allow yourself to feel supported after a diagnosis
Multiple sclerosis (MS) is currently classified as an autoimmune disease of the central nervous system (brain, spinal cord). MS is unpredictable and can…
Through thick and thin: Estelle and Adam’s MS love story
Guest post by: Estelle McLellan and Adam Laufer When Estelle and Adam first started dating, they never anticipated to have a third wheel…