What I Have Learned About Myself From Managing MS

I have learned that I can manage my MS through resourcefulness and looking for support when I need it. There have been challenges but if I look for it, I see the ways that I always was taken care of.

MS is a small part of my life

MS is only a small part of my life these days. I was diagnosed in 2003 at the age of 47. After attacks in 2004 and 2007, I left work on disability. Since then, I have faith that I will be alright. There were several ways I saw God taking care of me along the way.

The practical ways were financial. In the fall of 2003, pre-existing conditions were still an issue when getting health insurance. If I had been diagnosed earlier, I would have been on my employers health insurance with its 50/50 drug cost copay. Instead, I got on my husband’s insurance when I still didn’t think I had MS. I had a negative spinal tap and was ready to attribute my sensory symptoms to something else.

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Another financial gain was long-term disability insurance. I didn’t realize my employer had a policy on me, until I went from full to part time work and found out I could apply. I still remember the day in 2005. I was not sure how I was going to manage. We took my parents out to dinner for their 50th wedding anniversary. They were thrilled with the dinner and all I could think of was how I would manage to pay that credit card bill. Within a week, I got a retroactive disability payment and collected monthly payments until I turned 65 in 2021.

A higher power

It is not just after I was diagnosed that I saw God (or whatever you call your higher power) was there. I think my first MS attack was in 1991. I was under a lot of stress, driving an hour to work 4 days a week and working 10 hour days, while trying to manage as a wife and mother of two teens.

I started getting dizzy and having trouble seeing up close, only at work. So, one day, I just quit. Over the next few years I took several jobs until I landed the one I loved in 1996. That employer was the one that had the disability policy and allowed me to go part time in 2004 and was supportive when I left in 2007.

When I started writing this in answer to the question “What have I learned about myself,” I wasn’t sure what I would say. There is so much more to my story. I hope this little answer will inspire others to know you will be alright.

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The MultipleSclerosis.net team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

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