Latest Blogs
The Shame Behind Being Chronically Ill
There have been many times since my diagnosis of relapsing-remitting MS in 2015 that I… Read More
The Strong One
But there are some things, like a chronic illness, that simply cannot be fixed, and… Read More
Summer Retrospective… Yes, I Went There, I’m Looking Back
I’m so thankful for the ADA and for everyone who fought to make it a… Read More
Making Peace with My New Normal
It takes some time to reorient yourself to a different reality – to be able… Read More
What I Want My Legislators To Know About My MS
I want my legislators to know this more than anything though: there are about one… Read More
Wearing a Mask Is About Compassion
By wearing a mask, I feel I’m being compassionate to others, and by them wearing… Read More
Isolation During COVID-19: A Different Perspective
But oddly, unlike others, I have felt less alone during this quarantine and more accepting… Read More
Essential Work
I have MS, and I’m an essential worker. Face masks and social distancing aside, I… Read More
I get knocked down, but I’ll get up again
Recovering from a fall can be challenging. Read how one person gets up.
Staying above water with MS
One blogger describes finding support and learning to love life again after his MS diagnosis.
Breaking the cycle of exclusion: Embracing cultural competence in physical activity research for people with MS
Cultural competence in research involves considering the culture and diversity of a population.
Still Dancing: Overcoming MS to Become an Atlanta Falcons Cheerleader
An MS diagnosis in college didn’t stop Téa from cheering for the NFL.
Across the Other Side of the Pond, but Connected Through MS
An activist in the U.K. discusses the challenges that the Black MS community faces here… Read More