Yoga and Rehabilitation

In the beginning of 2018, I realized the benefits of yoga in managing my MS symptoms.

At Least

Horses gave me peace. They gave me freedom. They honestly restored my hope that I could do anything that I set my mind to.

My COVID-19 Vaccine Experience

I realize that doing this without a lot of recommendations could have been a bad idea, but I truly feel like it was the best decision for me.

MS During Isolation

It was odd going through the most challenging moment in my life without my family and friends nearby. We spoke on the phone and video chatted regularly, but it was not the same.

The Cane in the Room

Here’s a unique question: Because of my multiple sclerosis, I walk with a cane. Next week, I’m going to have a face-to-face interview for a job I really want.

Latest Blogs

speech bubbles on MS

MS Tidbits: Pithy Musings on Living with Multiple Sclerosis

Along the way I’ve thought a lot about how MS has affected my day-to-day life. I’ve… Read More

Turning a “Wasted Day” Into a “Healing Day”

As we shut out the lights and went to sleep that night, another thought came… Read More

What 2020 Taught Our MS Community

We start 2021 with renewed hope, inspired by the continued resilience of this community and… Read More

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

Returning to Work

I knew this was going to be a milestone year, but I had no idea… 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

speech bubbles on MS

MS Tidbits: Pithy Musings on Living with Multiple Sclerosis

Along the way I’ve thought a lot about how MS has affected my day-to-day life. I’ve… Read More

Turning a “Wasted Day” Into a “Healing Day”

As we shut out the lights and went to sleep that night, another thought came… Read More

What 2020 Taught Our MS Community

We start 2021 with renewed hope, inspired by the continued resilience of this community and… Read More

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

advertisement