Episode 0 – Pilot/backstory
The story of how Dan and Jen met after being diagnosed with two different forms of Multiple Sclerosis. They tell how they are able to be a caregiver for each other and be advocates for themselves and others with MS.…
The story of how Dan and Jen met after being diagnosed with two different forms of Multiple Sclerosis. They tell how they are able to be a caregiver for each other and be advocates for themselves and others with MS.…
A 30 second tease of the A Couple Takes on MS podcast.
A 1 minute tease of the A Couple Takes on MS podcast.
I wanted a sip of coffee this morning so I reached for the cup because, well, that’s what you do. And then I paused, because now, that’s what I do. What am I thinking? Hot coffee. Weak arms. This probably…
World traveler, renowned writer, MS patient leader, founder of ActiveMSers.org Welcome to “7 Questions with A Couple,” a monthly series that includes quick conversations with a variety of experts and influencers from throughout the MS community. We feel almost at loss…
No one likes to be left out. Feeling excluded is the worst. It leaves you feeling such doubt. Wondering why was I ignored or overlooked? More often than not, it’s not you, it’s them. Seriously! They’re the problem, not you.…
Award-winning writer, certified health advocate, creator of the blog An Empowered Spirit Welcome to “7 Questions with A Couple,” a monthly series that includes quick conversations with a variety of experts and influencers from throughout the MS community. We are…
Of course I’m a positive person, but I found myself in a place last Monday morning where I could comfortably shed my glass-is-half-full outlook. I was in the Mount Pleasant Health Park and was just told I had a 45-minute…
Dan often says I’m a social butterfly. That’s just how I am. I enjoy talking with others. Being friendly and getting to know other people’s stories. I like to smile and see where that takes me. Plus, I hope that…
Looking ahead to the promise of 2021 involves looking back on how far we each have come since we were diagnosed with Multiple Sclerosis. We mean, how the heck did we get the information we needed? Google and iPhones weren’t…