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…
In his hit song “Dancing in the Dark,” Bruce Springsteen said it best, “You can’t start a fire without a spark.” On September 28, 2002, the day Dan and I met, we found out that there definitely was a spark…
Dan and I have spent the past several months working with AnCan to organize and coordinate an incredibly important online event that will help families living with Multiple Sclerosis. We are beyond thrilled to invite you to “The Talk –…
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…
The irony of this past week’s events aren’t lost on Dan and me, and they should not be lost on you either. Here’s why. Just as Dan and I were finalizing a virtual meeting later this month with our United…
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…
This may sound like a foolish worry, but I am concerned that my husband, Dan, will never get drunk again. Yes, true, he probably shouldn’t get intoxicated because of his Multiple Sclerosis. But he is only 47 years old and…
Today was all kinds of special. It was the first-ever Virtual Walk MS event for a team of MS activists nationwide – MS Activists in Action. Of course Dan and I were totally on board when they invited us to…
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…
Here is the text from the letter we sent separately to our U.S. Senators Debbie Stabenow and Gary Peters encouraging them to make sure the next COVID-19 legislative package ensures people with MS get what they need and helps the…