Inspired by the light Dolly leaves behind
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.
Jennifer Digmann
Sometimes accessibility looks like community
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.
Caution: Emotions are closer than they appear
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.
Every step matters when it comes to MS and hope
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.
Fancy and free indeed
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.
A Couple takes on discipline
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…
Hope looks different after nearly three decades with Multiple Sclerosis
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…
We used to be the youngest people on the Michigan Capitol lawn
I noticed the Quality Supports Specialist from our Area Agency on Aging wiping away tears as Dan walked off the stage after delivering his speech at Older Michiganians Day (OMD). She leaned toward me and said how meaningful his words…
Light rain is no match for the reign of Walk MS Frankenmuth & Team MonsterS
There was a moment early that Saturday morning in May when the cold and forecasted showers made everything feel uncertain. Walk MS in Frankenmuth began under gray skies, steady rain, and the kind of weather that makes you wonder whether…
11 minutes, 1,900 seats, and not 1 for me: when accessible seating feels anything but accessible
Concert tickets might sound like a small thing, but for Dan and me, they’re not. Live music is one of our favorite ways to feel connected, normal, and joyful beyond the daily realities of living with Multiple Sclerosis. A couple…