Columns A Life in Letters – a Column by Jamie Hughes Getting in Gear: Essential Equipment for an Excellent Beach Vacation Getting in Gear: Essential Equipment for an Excellent Beach Vacation by Jamie Hughes | July 8, 2022 Share this article: Share article via email Copy article link The last few months have been a bit stressful, to say the least, and with the thousand and one worries and distractions I was facing, I couldn’t help but think of the opening lines of a William Wordsworth poem: “The world is too much with us; late and soon,/ Getting and spending, we lay waste our powers; —/ Little we see in Nature that is ours.” So our yearly beach vacation was much needed (and very much enjoyed by all). And apparently, we weren’t the only ones! Several other columnists have also been on the road recently, writing about how to combat fatigue while on vacation, as well as offering advice about new gizmos to deal with MS and heat sensitivity and to stay cool during the summer months. I was born in Arkansas, but raised in Florida, and throughout my childhood, I spent almost as much time in the ocean as I did on land. But sadly, that’s not the case these days. (Not being near water is one of the few drawbacks of living in Atlanta.) So I spend a lot of time prepping to make sure I can spend as much time on the beach as possible when we’re in Treasure Island, Florida, our preferred spot. Recommended Reading June 24, 2022 Columns by Ed Tobias Why I’m Giving 3 MS Medications Another Try One thing we’ve figured out over the years is that having the right gear is essential. Of course, I must worry about the heat, due to MS and heat sensitivity. That means a tent is essential. However, the tent we’ve been using — one of those 10-by-10-feet monstrosities that unfold like an octopus and weigh a metric ton — wasn’t really cutting it. We exhausted ourselves just dragging it down the beach and getting it set up! I decided that we had to find something lighter and easier to transport, and I found the perfect solution. It’s called the Sun Ninja tent, and it’s simply amazing. It folds down into a bag small enough for my younger son to carry, and it is super easy to set up and tear down. Because I’m in the shade and comfortable, I don’t have to cut my beach day short! The other thing we had to rethink was the cooler. We like to have plenty of sodas, water, and adult beverages to choose from throughout the day, but a hard, plastic cooler full of drinks and ice was a real pain to lug down the beach every day. After much hemming and hawing, we decided to go all in and purchased a Yeti backpack cooler and ice packs. (We don’t have this one. Ours is a slightly older model, but I’m sure this one works great, too.) The thing was a little heavy when it was fully packed, but my older son was more than able to carry it on his back. It kept the drinks cool all day, and there was no leaky ice to deal with when we got home. Living with MS requires adaptation. Sometimes, that means changing your plans entirely, and other times, only a few tweaks are required to keep the party going. Thanks to our tent and cooler, we were able to get to our spot and set up quickly, keeping the threat of fatigue in check and ensuring that we all had an excellent day on the shores of the Gulf of Mexico. Being able to relax and not worry about work (or MS) was exactly what I needed. Are you a fan of the beach? What are your “must-haves” for a day spent seaside? I’d love to hear what’s worked for you so I can keep refining our gear. Tell me all about it in the comments! Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today or its parent company, BioNews, and are intended to spark discussion about issues pertaining to multiple sclerosis. Print This Page About the Author Jamie Hughes Jamie A. Hughes is a writer-editor living in Atlanta, Georgia, with her husband, two sons, and a trio of very needy cats. She was diagnosed with relapsing-remitting MS in 2004 when she was just 25 years old. A lover of words since birth, she wasn’t about to let two little letters get her down. They don’t get the last word. And that’s why she writes her column — to help those dealing with MS to live more thoughtful, hopeful, and inspired lives. Tags heat, heat sensitivity, MS symptoms, summer, tips Comments Leave a comment Fill in the required fields to post. Your email address will not be published. Your Name Your Email Your Comment Post Comment
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