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Third Dose

For a person living with MS since 1990, the extra layer of protection I gained… Read More

stem cells multiple sclerosis

aHSCT: Who Might Benefit?

The National MS Society has endorsed aHSCT as an additional treatment approach for people with… Read More

Refocusing After an Unexpected Career Change

We never know what is around the corner. We have no control over challenges that… Read More

COVID-19 vaccine and MS

Why I Am Still Living in 2020

I wish you well and hope that you will discover and be willing to share… Read More

bladder problem MS

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

MS family

Sharing My Family’s MS Experience

There’s only hope on the horizon, and we’re coming together to make things better.

universal healthcare MS

Treating MS in a Universal Healthcare System

In the U.K., as you may know, we have the National Health Service (NHS).

sharing MS diagnosis at work

Sharing My MS Diagnosis at Work

This experience has taught me that it is OK to talk about my MS journey… Read More

comorbidities and MS

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

coping with MS diagnosis

Hand Lettering My Way Through Tough Times

During this time, I learned how helpful hand lettering is for me in tough times.

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