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…
Friendly Visiting: Staying Connected During COVID-19
Long before the pandemic, social isolation was an issue close to many hearts in long-term care. The MS Society’s Friendly Visiting program was…
A Look at the Women Against Multiple Sclerosis 2020
Since 2005, Women Against Multiple Sclerosis (WAMS) has brought together a powerful collective of professionals nationwide who fundraise and network in support of…
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…
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…
Stories on Women’s Health and MS
Women are 3x more likely to be diagnosed with MS than men. On International Women’s Day, we’re shedding light on some of the challenges faced…
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…
Beyond the Stigma
I was diagnosed with MS in 2011. Some people remember the day of their diagnosis like it’s an anniversary. They recall the weather,…
From Denial to Acceptance: A story about Catherine’s journey with MS
“For years, denial kept me from facing my MS head-on. Rather than learning how to live with it, I was ashamed of the…
