Latest Blogs
Saying Yes to Research
During one of my first visits with my neurologist, he asked me a question that… Read More
Lessons for the New Year
After all, one of the most important lessons we learned in 2020 is that we’re… Read More
Mealtime on Fatigue Days
If your mealtime doesn’t look like the traditional “family meal” experience, that’s OK. Your kids… Read More
Stuck in the Middle
I have a lot to be thankful for, but that doesn’t negate the fact that… Read More
MS Virtual World
I take every opportunity I have and participate in as many webinars as I can… Read More
Happy (Enough) Holidays
Don’t add more stress for yourself. This year has been stressful enough. Maybe this holiday,… Read More
20 Gift Ideas Under $150 That Keep MS in Mind
We’re sharing some gift ideas and favorite items from the MS community to help you… Read More
What Do You Want To See? My MRI Scans?!
This disability symbol includes all types of disabilities ranging from wheelchairs to a perfectly “normal”… Read More
The Joy and Meaning of Caregivers
I’ve realized since my diagnosis that a “life sentence” of MS can be just as… Read More
The Shame Behind Being Chronically Ill
There have been many times since my diagnosis of relapsing-remitting MS in 2015 that I… Read More
The Strong One
But there are some things, like a chronic illness, that simply cannot be fixed, and… Read More
Summer Retrospective… Yes, I Went There, I’m Looking Back
I’m so thankful for the ADA and for everyone who fought to make it a… Read More
Making Peace with My New Normal
Coming to terms with having a chronic, incurable illness like MS doesn’t happen immediately. It… Read More