An Unheard Voice: Amplifying Diversity in the MS Community
Guest post by: Moyna John Some days, I feel physically and emotionally fine; other days, I feel severely depressed. I miss when life…
The Four Stages of Processing my MS Diagnosis
Alanna’s story may sound familiar, perhaps all too familiar to some. At 25 years old, Alanna Palumbo was your quintessential self-starter: motivated, persistent,…
Millennials and MS: Andrea Veliz Garcia
There are questions about being a millennial with MS that you won’t find answered in any Google search. Like how do you think…
Dear Richard: A Letter To My Husband
Dear Richard, Five years. I feel like we’ve lived a lifetime in these last five years. It’s crazy to think how little we knew then. I…
The Equestrian Ride for MS: Raising Awareness in First Nations Communities
The Sioux Valley Dakota Nation Reserve, located west of Brandon, Manitoba, is home to the Dakota Nation Unity Riders – a group that…
Dear Marc: A Letter to my Husband
Dear Marc, If I had to write this letter shortly after being diagnosed with multiple sclerosis (MS), it would have had a much…
A Diagnosis Far from Home: Sogol’s Journey with MS
Being diagnosed with MS can be a frightening experience. It can be even more so when you’re far away from somewhere you’ve always…
#TakeActionForMS: Lance & the EI Sickness Benefit
“I disclosed my MS diagnosis to my employer almost immediately. I wanted them to know there was a genuine reason why things had…
Slipping Through The Cracks: My Invisible Disease in the Workplace
“I find people have a preconceived notion that if you can work full-time, you surely can’t be that bad. Because multiple sclerosis can be episodic and invisible,…
