When Cooper alluded in his last post that neither Dan nor I have been writing for our blog, I felt the need to explain what I’ve been doing. It was three weeks ago Wednesday, July 30, that I had Gamma-Knife Radiosurgery. This was the aggressive measure I needed to take in hopes it could control…… Continue Reading
Catch the Digmanns in the news
Author Archives: Jennifer
A New Voice
I see things. I have a great perspective and point of view. I’m smarter than people think. And I have feelings too! I get attached to people, especially caregivers, and it seems like as soon as I warm up to them, poof—gone. Just look at that list of successful caregivers over the last eight years.…… Continue Reading
Accessible road trip tips
I recently was watching our friends’ 7-year-old daughter, Abby, and while we were drawing at Dan and my dining room table, our conversation went something like this: “So are you excited about Easter?” I asked. Distracted by the work of art she was creating, Abby muttered, “Uh-huh.” Trying to continue our lively discussion I inquired,…… Continue Reading
Mr. and Mrs. Digmann go to Washington
Either our Multiple Sclerosis finally is starting to get to us or we really are getting old. Dan and I are leaning toward the latter (OUCH!). What else would explain how we have been back from Washington, D.C., for over three weeks and have not written about this incredible experience? The Michigan Chapter of the…… Continue Reading
What would you say?
Several weeks ago, our friends at Healthline reached out to us and asked if we would develop a video that helps those newly diagnosed with MS to adjust to life with the disease and reassure them that, “You’ve Got This.” Dan and I thought it was pretty empowering, and we liked that somebody wanted to…… Continue Reading
Mannequins and Disability
Mannequins and disability. Who would think of such a strange combination? And who would want to see images like those? After all disability is different and strange, maybe even a little scary. That differentness may explain why I would never expect to see images of the disabled as mannequins used in storefront windows. But that…… Continue Reading
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Hope everyone had a very Happy Thanksgiving! As the shopping season, or should that say Christmas season, begins today I thought this link would give you some great gift buying suggestions for anyone in your life, whether or not the person you are shopping for has Multiple Sclerosis. Happy gift hunting 🙂 Speaking of gifts,…… Continue Reading
My anniversary and MS community
Thursday, November 14, was my anniversary. But there were no cards or cake. I didn’t toast the day with a glass of champagne or by getting a bright, shiny new manicure. Instead, I cancelled my nail appointment and sat at home coughing and blowing my nose. I was sick with a cold and that spoiled…… Continue Reading
MS, Disability and Mickey Mouse
It’s a world of laughter, a world of tears It’s a world of hopes and a world of fears There’s so much that we share that it’s time we’re aware It’s a small world after all Be honest, how long did it take before you joined in singing this Disney classic? It’s infectious and I…… Continue Reading
Inspiration is all around
Not so long ago, it really would puzzle me when someone would tell me what an inspiration I was. Generally, I would smile, say thanks and think to myself, “You really should strive to find inspiration in something a little higher than me and my Multiple Sclerosis.” I mean, has anyone ever told you what…… Continue Reading