Wilbur VS MS
“I appreciate mobility. I appreciate being able to remember things. I appreciate being able to walk. Having gone through a period of time…
Taking MS into her own hands – and boxing gloves
At only 26, Jessica Faulds is thriving. She exudes the passion and determination most people aspire to have. Whether it’s with her fitness,…
Living day by day
The Multiple Sclerosis Society of Canada’s Vitamin D recommendations provide general information on vitamin D, where you can get vitamin D, how the…
An act of recovery: When treatments become triggers
Recovery : Noun /rəˈkəv(ə)rē/ The action or process of regaining possession or control of something stolen or lost. Some people living with multiple…
Reprioritizing my life to save it
Guest post by Kate Thompson, MS Bike ambassador That first year I was diagnosed with MS was hard — hard in so many…
MS research improves peoples’ quality of life
Guest post by MS Walk ambassador, Darcie opens up about how her neurologist’s foresight saved her quality of life. I like to think that I’m…
Captain Jack: A Canadian MS champion
By Judith Kays meets with curling champion and MS warrior, Jack MacDuff In 1976, Jack MacDuff led his curling team from St. John’s,…
How to talk about MS after you’ve been diagnosed
Diane’s story Diane sits quietly in the neurologist’s office collecting her thoughts. She’s just received a diagnosis of multiple sclerosis. It didn’t come as…
THREE’S A CROWD: MAINTAINING A RELATIONSHIP WITH MS
Jesse and Pat met at work, the way so many adults do after they graduate. On their first date, Pat introduced Jesse to…
