Talking about your Multiple Sclerosis can be challenging enough in conversations with your family and closest of friends. But how do you even begin to address this reality when you’re dating? When you meet someone in person, online or through…
It’s been a long time coming, but hooray! This episode marks the triumphant return of Ryan, our spectacular podcast producer! We take this opportunity (it’s been nearly three months since we’ve recorded together) to chat about everything including: Ryan’s role…
In this episode, Dan and I tackle one of the toughest questions: does the disease define us?
Listen to hear how we respond to this as we dig into what it looks like for us here in the middle of the month of March, which is Multiple Sclerosis Awareness Month. Learn more about the issues we addressed at the NMSS Public Policy Conference, the reasons why you (yes YOU!) are the best story teller, and how we connect onions and moldy bread to our lives with MS.
This includes nurses in hazmat suits, Jennifer going solo for a monoclonal antibody infusion, living fully masked for 10 days in our own house, and sleeping in separate beds for the first time in over 16 years of marriage.
Hey there, Listener Land. We’re going to skip this normally scheduled episode time for some quiet contemplation and rest. Our normal schedule should resume with a new episode in two weeks. Thanks!
“We look at everything through the lens of people living with Multiple Sclerosis. Covid-19 affects the entire population, but how does it affect two people with multiple sclerosis taking medication to control the progression of the disease …” Yes, it’s…
Businesses don’t find success just by winging it. They succeed because they have concrete mission statements and targeted objectives that guide them to pinnacle performance. Why should it be any different for you and the goals you set for yourself?…
A classic song of the holiday season gleefully encourages us all to believe this is “the most wonderful time of the year.” This is a great sentiment overall and in theory, but we also know it can be one of…
Do you ever feel guilty about having MS? Guilty, as though you deserve to have it or that it’s all your fault? We both have had MS for more than two decades, and we know we did nothing to deserve…
Jennifer and Dan discuss maintaining perspective and being thankful for what they have; positive things that MS hasn’t taken and positives they wouldn’t have without the disease in their lives.