
Living with MS Disability
Five years ago my life shifted and the disease gained momentum. Despite my best efforts, it knocked me down like a tsunami. I keep getting back up each time, but so far the waves have been relentless and they just keep coming. It feels like just when I recover from the last blow and adapt to a new normal, another one comes out of nowhere and knocks me over again and I’m like: really?! Haven’t I had enough? How far will this go? Life humbles you. You learn that there are things that are not always in your control. That life isn’t always fair. That nothing is really guaranteed. I’ve also learned, though, that you may not always be in control of what happens to you, but you can always control your reaction to what is happening. Living with MS disability is hard physically and emotionally and in some ways it feels like every day is a battle. But I won’t let this battle define me or get the best of me. There are other things I can focus on and so many blessings in my life I can celebrate. Every single day I make a choice that I will live my best life possible in this body that I have been gifted, despite its limitations. I see every day as a gift and an opportunity to be happy. I’ve made the decision that no matter what life throws my way, I will adapt and overcome it. I’ll never stop making goals for myself and persevering even though it feels harder to accomplish things than it was before. Being disabled has opened my eyes to what is truly important in life and allows me to better appreciate the things that really matter.Give Yourself Grace with a Mobility Aid
It takes courage to accept that you need a mobility aid and to do it with grace