Latest Blogs
Sharing My Family’s MS Experience
There’s only hope on the horizon, and we’re coming together to make things better.
Treating MS in a Universal Healthcare System
In the U.K., as you may know, we have the National Health Service (NHS).
Sharing My MS Diagnosis at Work
This experience has taught me that it is OK to talk about my MS journey… Read More
MS and Something Else: 7 Tips to Manage Your Chronic Disease and Comorbidities
Here are 7 tips that have helped me along the way in juggling comorbidities and… Read More
Hand Lettering My Way Through Tough Times
During this time, I learned how helpful hand lettering is for me in tough times.
Decision Time: COVID-19 Booster (Additional) Shot & MS
This is how it is living with a chronic, incurable disease. I have to make… Read More
The Challenges of an MS Warrior
Just as every person is unique, MS is unique in each person, which makes it… Read More
The Cost of Caregiving
Caregiving allows us to tackle this disease as a unit, but its cost can sometimes… Read More
Your Story Matters
Somewhere along the way, it became easier for me to talk about my multiple sclerosis… 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