NEWS & POSTS
After nearly 30 years of living with Multiple Sclerosis, Jennifer has learned that MS may always be along for the ride. But that doesn’t mean it gets the keys or gets to decide where she and Dan are headed.
More than 13 years ago, Dan compared living with Multiple Sclerosis to running straight ahead on the football field. After another weekend of yelling at the TV, he realizes the philosophy still holds.
A simple reminder on our bathroom mirror takes on new meaning as Jennifer reflects on Dolly Parton, the light she brought into the world and the light we all have to share.
A ticketing oversight left Jennifer without an accessible seat at one of the summer’s biggest concerts. What happened next became an unforgettable reminder that sometimes accessibility looks a lot like community.
Some days our emotions sit just beneath the surface, leaving us wondering why everything feels a little heavier. Jennifer Digmann reflects on living with Multiple Sclerosis, choosing grace over answers, and discovering that even tender hearts possess remarkable strength.
Meeting coworkers in person for the first time made me wonder what they'd think of the physical effects of Multiple Sclerosis. What happened instead taught me an unexpected lesson about identity, relationships, and the people who truly know us.
The Central Michigan University Physical Therapy students are taking meaningful steps to support the National MS Society through the 2026 Conquer MS 5K. Learn why this event means so much to us and why we'd love for you to join us.
What began as a patriotic church celebration became a powerful reminder that freedom isn't always defined by our circumstances. Jennifer reflects on faith, fellowship, gratitude, and discovering the joy that remains untouched by life's challenges.
It has been almost 21 years since Dan and I got married. When I think about all we have experienced together—Multiple Sclerosis, caregiving, advocacy, speaking, writing, and simply navigating everyday life—I am incredibly grateful. But lately, I’ve realized something. We…
The future felt uncertain when Dan and I were each diagnosed with Multiple Sclerosis back in 2000 and 1997, respectively. There were treatments available, but the options were limited. Many of the conversations centered around managing symptoms and slowing disease…