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…
Here is the reality when Dan and I write about the work we’re doing as MS advocates: we aren’t in these efforts by ourselves. We often are joining other advocates in the MS community to make the biggest impact in…
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.
We are so humbled and honored – as March officially is MS Awareness Month – to share our conversation with Jon Strum. If you are living with MS or are involved with the MS community, Jon likely needs no introduction. If you aren’t familiar with him, he is a powerful advocate and voice (literally check out any of his excellent, informative RealTalk MS podcasts) for the nearly 2.8 million people throughout the world living with the disease.
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.
This essay I wrote for MultipleSclerosis.net goes inside my emotions and fears during my entire Covid experience. What is extra special about this article is that its posting ties into National Caregiver Day, which this year is February 18.
We’re going to take one more break. We all found our comfy spots JUST while we were ending the last break, so we decided to stay bundled up and give this one a miss as well. Seriously, though; we’ll be…
We are beyond thrilled to introduce Hannah Garrison as our first 7 Questions with A Couple guest for 2022. Hannah is an incredibly talented visual artist who has inspired people nationwide and turned them into artists in their own rights through her virtual online art project sessions and demonstrations.
This was an important essay for me to write because I really wanted to provide some insights into using Botox to control bladder issues related to MS and help other people who have questions about this way to treat this common MS symptom.
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!
