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.
Category Blog
NEWS & POSTS
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.
What my colleagues saw in Chicago
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.
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…
100 podcast episodes later, we’re still moving forward
When Jennifer and I launched the podcast for A Couple Takes on MS, we hoped it would spark honest conversations about life with Multiple Sclerosis, caregiving, advocacy, and marriage. We did not expect it to become such an important part…