An Outing Among the Healthy: Batter Up!

An Outing Among the Healthy: Batter Up!
I finally made it to a baseball game! I was feeling well enough to attend and the sky was blue with tolerable humidity. But I hadn't taken into account another important factor: My husband. Aside from chronic back problems, he has spring and summertime allergies. The day before, he had suffered a massive sinus headache that incapacitated him. While I reminded him that it was important that we both felt well enough to enjoy the game, I admit a selfish part of me was doing a Donald Duck-style temper tantrum inside over how one event would involve so many obstacles. Late morning, I began to feel a bit of burning pain around my ankles, which told me the humidity was increasing. That turned out to be the case. I was prepared with Neurontin (gabapentin) and cool wraps to apply on my ankles, should the symptoms worsen. I already had researched the commute (i.e., time frame, how busy, amount of walking) and stadium (route to seating, concessions, bathrooms), so I felt confident to handle most situations. The sights and sounds were mesmerizing. As those who have been to a live concert or sporting event know, it varies from what is seen on television. The excitement was definitely a huge emotional boost for me, as well as a physical one. A beautiful day, warm weather, a breeze to mitigate the humidity — all while enjoying the sights and sounds of a baseball game with my husband — was wonderful. It was not until about the sixth inning that my body
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4 comments

  1. SrevefromMA says:

    Good for you, Lori!

    Every time I read an account like yours, I realize again that no one but us really understands the extreme pain and discomfort from FM, no matter how well they know us or have heard us (me) complain.

    • Lori Galpeer says:

      Seems like it sometimes. When someone, like my hubby, who knows FMS almost inside and out, doesn’t understand something I am discussing, I am taken aback. I tend to forget that they are still experiencing this second-hand and tend them to understand everything. Sometimes feel surprised or hurt that am ‘alone’ in this among my loved ones who don’t have the illness. Thankfully there are so many of us w/ FMS that can thoroughly understand all too well. Hope you are doing well!

  2. Jena says:

    I am new to this newsletter and reading stories from other people who actually suffer fibro as well. Makes me know I am not alone and you understand what it feels like to live with this disease. Thanks so much for sharing.

    • Lori Galpeer says:

      Thanks for sharing too! The intention of my articles is definitely to show we are not alone; while FMS can differ in the degree and length of time with symptoms – we all can understand as well as the magnitude in which it affects us. Feel free to share and comment any time! 🙂

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