Latest Blogs
Why I Am Still Living in 2020
I wish you well and hope that you will discover and be willing to share… Read More
My Terrible, Horrible, No Good, Very Bad Bladder
It’s okay to take 100 bathroom breaks in 30 minutes; it’s okay to need to… Read More
Sharing My Family’s MS Experience
There’s only hope on the horizon, and we’re coming together to make things better.
Treating MS in a Universal Healthcare System
In the U.K., as you may know, we have the National Health Service (NHS).
Sharing My MS Diagnosis at Work
This experience has taught me that it is OK to talk about my MS journey… Read More
MS and Something Else: 7 Tips to Manage Your Chronic Disease and Comorbidities
Here are 7 tips that have helped me along the way in juggling comorbidities and… Read More
Hand Lettering My Way Through Tough Times
During this time, I learned how helpful hand lettering is for me in tough times.
Decision Time: COVID-19 Booster (Additional) Shot & MS
This is how it is living with a chronic, incurable disease. I have to make… Read More
The Challenges of an MS Warrior
Just as every person is unique, MS is unique in each person, which makes it… Read More
The Cost of Caregiving
Caregiving allows us to tackle this disease as a unit, but its cost can sometimes… Read More
MS Clinical Trials and Unlocking Your Inner Fighter
I received an email from the National MS Society regarding a clinical trial to investigate… Read More
Missed-Diagnosis : My 4 Early Signs of MS
I’m a smart woman, but even with my level of intelligence, I was ignorant to… Read More
To My Fellow Men With MS
I hope this has helped open the mind of those men who have MS or… Read More
Little Engine That Could
I just thought to myself, isn’t that a story we, those who live with MS,… Read More