One new way I keep moving with MS
I never thought I needed a Cubii … until I got one. I mean, come on. I have a full-time job and work remotely, so if I ever needed a break to give my mind a rest and burn some…
I never thought I needed a Cubii … until I got one. I mean, come on. I have a full-time job and work remotely, so if I ever needed a break to give my mind a rest and burn some…
I told Dan that I still remember the last big, long walk I ever took like it was yesterday. My first physical therapist, Heather, and I were at the Bower Theater in Flint, Michigan, to see the musical “La Cage…
Jennifer and I have known for years that Multiple Sclerosis affects everybody differently. But we quickly are learning that not all MS patients are attacking their disease the same way. Yes, it is a generational thing. For real. Generational. We…
Dan is a paid ambassador for Celgene, and collaborated with Celgene to create this post. Knots tightened in my stomach as I seemingly stood by myself in an open New Jersey field. I watched the wicker basket gate close quickly…
CONTACT US We welcome contact from anyone with questions, event bookings or even just if you’re having a bad day and need support. SUBMIT
EVENT BOOKING Book the Digmanns for your next event! Wherever you are on your Multiple Sclerosis or caregiving journey, here are two people who get it. Dan and Jennifer Digmann will share perspectives on life from a husband and wife…
TESTIMONIALS WHAT PEOPLE SAY “Dan and Jennifer are magnificent ambassadors and activists for anyone living with MS. Their story and approach to life and each other is real, funny, challenging, encouraging, and spiritual. I cannot think of a better couple…
ACCOLADES
IN THE MEDIA Photo by Emily Mesner featured in her story “Overcoming Battles with Love” Jenn Talks to Dan and Jennifer Digmann, a Couple with MS Multiple Sclerosis News Today’s The Multiple Sclerosis Podcast with Jenn Powell September 2022 Multiple…