When Jennifer and I met, two things she wasn’t sure about me was that I was a HUGE Bruce Springsteen fan and that I loved baseball. But she liked me and was willing to give both a try because she…
Jennifer and I recently partnered with Healthgrades to share “My Multiple Sclerosis Confession.” In this short video, we needed to include a dramatic moment when living with MS. Apparently my drama raised more questions than answers about a certain bat…
For families living with Multiple Sclerosis, here’s a free virtual “The Talk” event just for you! Register today for “Multiple Sclerosis …. Speaking to Your Family About Your Disease” to get insights from Dr. Aaron Boster and four families nationwide…
Yes, September 10, 2020, marks 15 years since our wedding day! What a better way to remember this day than share this article I wrote about it that originally appeared in the membership magazine of the National MS Society (Inside…
Voting, MS and the November 3 election Welcome to “7 Questions with A Couple,” a new monthly series on our blog that will include quick conversations with a variety of experts and influencers from throughout the MS community. For our…
I fear that others living with an invisible disability are going to hate me for what I’m about to say. We likely all have heard stories or perhaps encountered people in parking lots pulling up and chastising those who park…
Jennifer and I are excited to share these current opportunities (many are coming up this month) for you to get involved with us in making a difference and making the connections that will help you and others to move forward…
Perhaps my crystal ball was a bit foggy, but I didn’t know what my life was going to look like after I was diagnosed with MS over 21 years ago. Would I continue working? Would I stay healthy? Would I…
We’ve shared our stories, experiences and perspectives from our lives with Multiple Sclerosis with people here on our blog for nearly 12 years. Our written words sparked conversations, inspired our first book, encouraged others living with MS and humbled us…
People often comment that Jennifer and I are lucky because we live with someone who truly understands Multiple Sclerosis. But even before the realities of COVID-19, we understood the importance of maintaining good relationships with others. This is why I…