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…
Founder and owner, MS Scents Candle Co. Dan and I are thrilled that LaToya Johnson agreed to share her valuable insights, wisdom and perspective to our 7 Questions with A Couple series. She is the dynamic owner of MS Scents…
Edie Sohigian had no intention of focusing on Multiple Sclerosis when she developed the direction of her podcast. Sure, she has a first-person understanding of what it’s like living with MS – Edie was diagnosed in 2015 – but she…
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.
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 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.