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Radical Self-Love: Sacred, Not Selfish

Is Self-Love Selfish? Let’s Chat. I saw a post on Facebook recently that asked,“What’s one piece of advice every child should get?” Without thinking twice, I wrote:“Love yourself unconditionally.” Later that day, I asked Jeremy what he’d say.He goes, “Be kind.” Also great advice. Nailed…

Tysabri injections, nice idea

After 10 years, Tysabri is evolving to become simpler to administer. One of the strongest MS drugs, and up until a few years ago, the only ‘highly effective’ treatment available, has involved an afternoon spent in hospital every four weeks. Only dispensed at regional centres,…

Marrakesh: when attitude outweighs infrastructure

A fairly impulsive holiday to Marrakesh this spring, when I was just craving some heat and sun (and easyJet obviously sensed the vibe and launched sales). I didn’t expect an old African city to be super accessible, but it had got to the point where…

MS And The Fear Of Losing Independence

My latest MS meltdown happened inside a trendy motel in the middle of nowhere Northern Ontario. The Banker and I were on a 2-day mini-break, but the break I really needed was from my body, and my body was like, “Yeah, that doesn’t work for…

Research Highlights from ACTRIMS Forum 2023

On February 23-25, 2023, the eighth annual Americas Committee for Treatment and Research in Multiple Sclerosis (ACTRIMS) forum took place in San Diego, California with the theme – MS: Going Viral. This was one of the largest ACTRIMS meetings to-date with over 1,800 participants in…

Why Not Me?

Guest post by: Lindsay Ireland  I believe in the power of perspective. Reframing the narrative in my head may not cure MS, but it has helped me live my best life. Living with three autoimmune diseases, this outlook has proven its value to me many…

Black History Month – Meet Luidjy

“I cried a lot when I was diagnosed. I was 22 years old, and I thought my life was over.   I went to the hospital after losing feeling in my right arm. While I was there, I lost feeling in my right side, from my…

Black History Month: Meet Kelly-Ann

“Over a decade ago, I experienced numbness in my legs, and it progressed until I had no feeling in my left foot. I remember my neurologist talking about MS while I stared at the Parkinson’s poster that was plastered on the wall behind him. I…