I Feel Like I Have MS Today ( a patient’s story)
By Dianne Scott – January 5, 2026 Roses are red, violets are blue; every day is not a bad day, but…
Men’s online MS Group asking other Men with MS to Join the Conversation
A diverse community of men disabled by MS, currently meeting by Zoom. Most attending bear a classification as primary or…
Stuart Schlossman
What People SHOULD Say to Someone Living with Multiple Sclerosis
By Cathy Chester Last Updated: April 1, 2025 There’s a marvelous piece written by Ashley Ringstaff called “MS & Things People Should…
Stuart Schlossman
Being honest with myself about MS pain isn’t the easiest thing to do
Written by Benjamin Hofmeister | January 22, 2026 Over the years, I haven’t always followed the same advice I’ve given others. For instance,…
Stuart Schlossman
Losing my sense of safety after an MS relapse
With my body in collapse, silence engulfed me by Ahna Crum | October 21, 2025 During my hospital stay earlier this year, all I could…
Stuart Schlossman
When living with MS, we have to be open to change in our routine
When this disease changes our abilities, it’s important to adapt “We’ve always done it this way” was the phrase I…
Stuart Schlossman
I am a warrior. I am my own advocate, and I will prevail.
Just about a month ago, I was feeling like crap. I had a difficulty walking through an airport without being…
Stuart Schlossman
Guest Voice: What ‘It’s a Wonderful Life’ teaches us about living with MS
Like the film’s protagonist, my life today is smaller than I imagined by Donald Kushner M.D. | August 15, 2025 Donald Kushner, MD,…
Stuart Schlossman
Making Waves on Capitol Hill – An MS Patient Helps to Make a Difference
In early April, Jeanette Ashlock sat confidently in a front row seat before Congress. While her MS diagnosis had been…
Stuart Schlossman
The Midnight Bathroom Run From Hell – a patient’s story
When you can’t walk, a simple middle-of-the-night trip to the bathroom is anything but. By Mona Sen For My Health Story…
Stuart Schlossman
