Living with Multiple Sclerosis involves plenty of work people never see. We talk about the extra planning, accessibility, caregiving, adaptations, and patience behind continuing to show up and do the things that matter.
After more than 25 years of living with Multiple Sclerosis, we’re discovering there’s still plenty to learn about gut health, diet, and inflammation and what we can control along the way.
What do sex, drugs, and rock and roll have to do with living with Multiple Sclerosis? More than you might think. We talk disability, healthcare, medication access, accessibility and the importance of advocating for yourself.
Editor’s note: As students prepare to head back to school, we’re excited to revisit one of our favorite conversations. Children are naturally curious, and the way we answer their questions about disability can shape a lifetime of understanding, kindness, and…
As we grow older, it isn't always easy to know whether changes are caused by aging or multiple sclerosis. After attending a webinar with Dr. Aaron Boster, we're discussing healthy aging, disease-modifying therapies, protecting functional reserve, and practical ways to continue living well with MS.
After neurologist appointments, MRI results, and encouraging news, we're reflecting on what stability really means after decades of living with Multiple Sclerosis—and why finding the right healthcare team can make all the difference.
“We aren’t looking for answers yet. We’re learning how to sit with the questions.” As we prepare for an upcoming appointment with our neurologist, a simple question from Jennifer sparked a conversation neither of us expected to have. What if…
“For a long time, I assumed caregiving was simply what spouses do. Then hernia surgery showed me just how much family caregivers carry every day.” We have participated in Older Michiganians Day at the Michigan State Capitol for more than…
“Is it ever enough… or are we always waiting for the next breakthrough, the next voice, the next reason to hope?” We found ourselves in an unexpected place for this episode: talking about Multiple Sclerosis (MS) through the lens of…
“How would you feel if everybody’s talking about you behind your back? You need to be talking to the actual patient.” Just days before our conversation for this episode, Briana Landis was on Capitol Hill advocating for the Multiple Sclerosis…