New ventures lead to new found bonds
Guest post by: Carrie MacLean When I was diagnosed with multiple sclerosis (MS), I thought I only had a few years to live.…
Millennials and MS: Abdalla Ahmedin
There are questions about being a millennial with MS that you won’t find answered by a Google search. How do you think about…
Indigenous People and Multiple Sclerosis
Multiple sclerosis (MS) is a disease that does not discriminate – it can affect anyone at any time, often in the prime of their lives. In…
Faces Behind the Science: Kelsi Smith
Kelsi Smith is a Canadian who is pursuing her PhD in the area of neuroscience and epidemiology at Karolinska Insitutet. In 2020, Kelsi…
MS Navigators – pillars of support
A diagnosis of multiple sclerosis (MS) comes with unanswered questions. Your medical team can provide expert advice on halting disease progression and available…
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…
