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A Couple Takes on MS: A Couple Takes on MS – Dan & Jennifer Digmann
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This post would never end if I shared every photo from 2025. And, honestly, that wouldn’t tell the real story anyway.
So, I gave myself a boundary: two photos per month. Not too little, not too much. Just enough to capture the moments that made me pause, laugh, adapt or feel especially grateful.
This is the year ...
The hardest part of my Multiple Sclerosis Rituxan infusion isn’t the struggle to find a plump vein for an IV placement, or the five hours Dan and I spend in the infusion center, or even the fatigue that follows.
The hardest part is the dose of
Caregiving couples like Jennifer and me perform a dance every day that no one ever teaches you.
There’s no studio. No choreography sheet. No one calling out the counts. And yet, somehow, we learn the steps through repetition, trust, and a ton of trial and error.
Photo by Emily MesnerHonestly, it probably deserves a name.
...I never could have imagined that exactly 28 years after being diagnosed with Multiple Sclerosis, I’d find myself on a runway in Fort Lauderdale, Florida—modeling adaptive clothing, no less.
And I certainly never imagined I’d be modeling adaptive clothing with my husband. But that’s exactly what happened on November 14, 2025. Just. Wow.
It wa...