Episode 61 – Eye see you, MS
Sometimes what other people are seeing seem so obvious to them. “How could you not see it?” they ask. Maybe you could see it but just not very clearly. You don’t want to face the truth that your vision is…
Archives Episode
Episode 60 – Take a look into our MS caregiving experiences
There’s more to our relationship than 18 years of marriage and each of us living with Multiple Sclerosis. We also are in a caregiving relationship. Jennifer is my primary caregiver, and I am hers. We were so humbled and honored…
Episode 59 – How do you perceive challenges in life & with MS?
Do you approach life’s challenges from the glass is half-full or the glass is half-empty perspective? Or, are you like Jennifer’s friend Nora and think, “This isn’t the drink I ordered.” None of us really have a choice in the…
Episode 58 – Taking on MS & August recess visits
If a bill goes before Congress and you never told members how their actions will impact you, how confident are you that they will vote in your favor? As two people living with Multiple Sclerosis, this isn’t a chance we’re…
Episode 57 – Taking on traveling, road trips & MS
It’s challenging enough living with Multiple Sclerosis when you are settled into the comforts of your home, but the stresses compound when you venture out on an overnight trip. Gone is your strategically crafted accessible environment and you find yourself…
Episode 56 – Taking on MS & asking for help
A listener recently submitted a question to us through acoupletakesonms@gmail.com wondering, “How does someone just diagnosed with MS (or even someone who has lived with MS for some time) find the courage to ask for help?” What an incredibly insightful…
Episode 55 – Taking on handling the heat & MS
Heat is akin to kryptonite when it comes to many people who are living with Multiple Sclerosis. In fact, studies have shown that this “many” accounts for 80% of us all, including the two of us. Summer officially launches on…
Episode 54 – Taking on MS & inclusion with Julie Stamm
Dan and I have lived with Multiple Sclerosis for more than two decades and have had some incredible opportunities courtesy of the chronic illness. We’ve advocated in Washington, D.C., written and published a book; rode in a handicap accessible hot…
Episode 53 – Taking on MS & mourning sickness
Experts often describe grief in five or seven stages. If only life with Multiple Sclerosis could be so efficiently contained. Shock. Denial. Anger. Bargaining. Depression. Testing. Acceptance. This all can happen each day before we get out of bed. Yes,…
Episode 52 – Taking on PT & exercise with Heather Schoen
This an episode that got very personal for the two of us, but Jennifer took it even more personally. What an amazing moment to have a candid conversation about physical therapy, exercise and Multiple Sclerosis with Heather Schoen – the…