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MS Stories
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Tara from Colorado, USA

We have asked MS warriors to share their experience with MS and having a rollator. This is Tara’s story:

“I started showing MS symptoms in 2012, after the birth of my second daughter. I started using a rollator in 2016. At first, I only used it at home, and I was really embarrassed about needing a mobility aid in my 30s.

At first, using a rollator was hard to accept. It felt overwhelming to be losing my mobility due to MS at the same time I was raising a young family. Over time, I realized that using a rollator made it easier for me to be a better wife and mother because I could do more with less effort. I had only used a cane a few times, so using a rollator was a big adjustment but also a big help.

I use a rollator every day when I am on my feet. I also use a wheelchair sometimes now. But my rollator is still one of my most frequently used mobility aids.

Using a rollator has changed my life for the better. I can accomplish more things and stay on my feet longer when I use it. I can also go outside and enjoy activities with my family more often. Learning how to use a rollator has been one of the most helpful tools along my MS journey.”

“Over time I realized that using a rollator made it easier for me to be a better wife and mother because I could do more with less effort.”

– Tara on starting to use her rollator more publicly

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Tara’s best rollator tips:
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  • View your rollator as a tool that helps you to live better. Maybe even call it an “accessory”.

 

  • Wear clothing that you feel confident in. When you stand tall and feel good about yourself, a rollator is easier to use.

 

  • Give yourself grace. It can take time to adjust to a new MS diagnosis and/or using a mobility aid. It will get easier!