caregivers Archives - Blog - MS Society of Canada

For the Love of MS

Guest post by: Devin Meireles It was the winter of 2012 when my girlfriend and I got ready for a new horizon upon…

by Amy Baldwin February 8, 2022 Comments1

At some point in their lives, nearly half of Canadians aged 15 and older have provided care to a family member or friend…

by Mari Satoh February 20, 2019 Comments1

Community

Dear Amelia, A few months ago, you wrote me a letter – a letter about what it feels like to be my caregiver…

by MS Society of Canada June 17, 2018 Comments1

Community

Dear Dad, I will never forget when you were first diagnosed with multiple sclerosis. It was ten years ago and I was only…

by MS Society of Canada April 3, 2018 Comments5

Advocacy

A caregiver is a person who takes on an unpaid caring role for someone who needs help because of a physical or cognitive…

by Meaghan Kelly April 4, 2017 Comments3

Community

Guest post by Kirsten Mooney, MS Walk ambassador Over the years, my mother and I switched roles – I became the caregiver.…

by Guest post April 5, 2016 Comments2

Advocacy

Last week, the Canadian federal government released the 2015 budget. What does this mean for Canadians with multiple sclerosis? In this post, I’ll…

by Neil Pierce April 29, 2015 Comments3