Walk MS 2019

If I already blogged about this, forgive me. I’m just pretty sure I didn’t, so you’re getting this report a month late.

So! In May Mindy’s Minions gathered again to walk 3.1 miles around the capitol city in support of everyone living with multiple sclerosis. This is such a fun and lighthearted event, but it also does so much good, seriously.

The National MS Society puts on this event, and I am always eager to support them because they have been such a huge support to me from the beginning. Even before I was diagnosed with MS in October 2009 they helped me. During that summer, I had this strange and painful itching in my right arm. I was googling on the interwebs to find out what could be causing it, and I stumbled on their website. What I found was a detailed description of my symptoms, one far more detailed than I could have written. In short, they nailed it. I remember the moment so clearly. I was on my lunch break, sitting in my cubicle, and I had to hide the tears that were rolling down my face. I knew at that moment what I had, and I was terrified.

I was later diagnosed, of course, and the Society helped direct me to support groups for people like me. The first group I walked into was probably 80% older folks who were confined to wheelchairs. So, again, I was terrified. I thought I was staring into my future. It wasn’t until I found a support group for people my age that I started to have some real hope. Our group is a little more dispersed now and doesn’t meet in person anymore, but we still offer each other regular support through a private Facebook group. We share our struggles and our victories, we talk about our changes in diet, exercise, and medications. We are there for each other when we feel like no one else can understand. It’s been a true gift to have these people in my life, and I wouldn’t have them if it weren’t for the National MS Society.

So I raise money to give back. I walk, WE walk, to show our support. It’s an exercise in solidarity. I am surrounded by amazing family and friends all year long, but this day is special to me. It’s a day for my family and some of my dearest friends to come together and show their official support of me and my battle with this awful disease. I could not fight this alone and I am truly grateful to have these people in my corner.

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