Jennifer and I have shared personal stories about our life with Multiple Sclerosis for more than 20 years. They’re what we know. But it’s always humbling when other people connect with us because they want to know more about our…
When life sounds an alarm, do you snooze it or consider it a wake-up call? A two-block walk to watch the Great Lakes Loons this season was a rude awakening for me in the face of my life with Multiple…
I’m not content with settling for the adage that laughter is the best medicine. That is, not after Jennifer and my quest to see our favorite comedian John Mulaney taught us that the pursuit of laughter had the power to…
President and Founder of MS Views and News We often comment that knowledge is power when it comes to living with Multiple Sclerosis. A person who knows this far too well is Stuart Schlossman. He is the President and Founder…
It was easier for me to think I was being stubborn rather than admitting I was afraid. Living with Multiple Sclerosis for 22 years will do that to you. At least, it did that to me. I never wanted to…
We’re still a little blown away with this reality: Jennifer and I are going to be featured in an hour-long LinkedIn Live event that will include an in-depth discussion about living with Multiple Sclerosis while supporting a spouse with the…
NMSS Healthcare Provider Engagement Manager, MS activist Jennifer and I are blessed by the many great people we have met in our MS community. These are the people who continue to inspire us and provide the support we need to…
MS advocate, founder of Must Stop MS and #ChatMS Randy Patrick didn’t let his Multiple Sclerosis diagnosis stop him. In fact, his diagnosis was the beginning of his story and mission – to raise awareness and provide support for the…
Think about the different cliches that relate to outward appearances. Here are a few to get your mind going: • “Don’t judge a book by its cover.” • “Looks can be deceiving.” • “It’s better to look good than to…
We are adamant that Multiple Sclerosis doesn’t define who we are. It just happens that we are two people who happen to both live with this chronic progressive disease. MS doesn’t define Jennifer and me; rather, we are doing what…