Got MS? Gotta go? Gotta watch this webinar with Dr. Rubin
My biggest concern when I was diagnosed with Multiple Sclerosis waaaaaay back in 1997 was what the disease would do to my ability to walk. I started working with a physical therapist quickly after my diagnosis because I knew the…
7 Questions with A Couple featuring Al Thieme
Founder and Chairman of Amigo Mobility International Welcome to “7 Questions with A Couple,” a monthly series that includes quick conversations with a variety of experts and influencers from throughout the MS community. We are grateful that Al Thieme took…
Register for “Multiple Sclerosis and Urological Issues” webinar
These brief facts from the National Multiple Sclerosis Society speak volumes about two symptoms that impact an overwhelming majority of people living with MS: • Bladder dysfunction occurs in at least 80% of people with MS. • One study of…
#TBT – but i wanted to clean that up!
Welcome to this Throwback Thursday post on A Couple Takes On MS, where we repost some of our favorite essays over the past 14 years since we launched our blog. These appear on the last Thursday of each month, and there…
#TBT – Jim Harbaugh and my MS
Welcome to this Throwback Thursday post on A Couple Takes On MS, where we repost some of our favorite essays over the past 14 years since we launched our blog. These will appear on the last Thursday of each month,…
MS, REO and grown-up choices
Perhaps I am showing my age, but I am a big fan of the 80s rock band REO Speedwagon. My college years memories are filled with my good friend Amy and me being on the grassy hill at DTE Energy…
How do you disease modify your MS?
Five hours from start to finish. Really, four hours is more accurate. The entire bag of Rituximab flowed through my body in four hours. Pretty good, if I may say so. That first hour was spent trying to get my…
#TBT – Blessings counted … even in the bathroom
Welcome to this Throwback Thursday post on A Couple Takes On MS, where we repost some of our favorite essays over the past 14 years since we launched our blog. These will appear on the last Thursday of each month,…
MS caregiving in 3 acts
Over our last 16 years of marriage, Dan and I have learned a lot about what it means to be each other’s primary caregiver. In fact, we learn something new about caregiving every day because much like multiple sclerosis, no…