Columns Dive to Fight MS - a Column by Mike Parker Who knew that zip lines are a way to give back to the MS community? Who knew that zip lines are a way to give back to the MS community? This columnist has already jumped out of a plane. Here's what's next by Mike Parker | April 3, 2024 Share this article: Share article via email Copy article link Given how much my life has changed because of multiple sclerosis (MS), anytime an opportunity arises for me to support an MS charity, I jump at the chance ā figuratively, of course. I recently learned that the MS Society UK is organizing another of its zip line events in June to raise funds. Letās be honest: It isnāt quite like jumping from an airplane at 10,000 feet, which I did last October, but it is something I’ve never done before. So I signed up and started to raise funds. Why do I support these charities? From the moment my general practitioner told me to expect an MS diagnosis back in February 2022, I knew I’d need to talk about my fears and feelings. While searching online, I found the MS Society UK and their help line. After some soul-searching, I made a call and explained how I was feeling. Recommended Reading March 28, 2024 Columns by Benjamin Hofmeister Multiple sclerosis awareness is for people with MS, too The help and advice I received were invaluable. The call center staff explained the condition and what to expect from upcoming tests, including MRIsĀ and lumbar punctures (also known as spinal taps). They eased my fears by being calm and listening to me. From then on, I wanted to start giving back with the hope that my small efforts could assist the charity in continuing to help others. To date, Iāve been involved in two 5-kilometer walks around London, mostly done in my wheelchair. Both events were fantastic, and I raised a few hundred pounds while seeing some of the cityās best landmarks, including Big Ben, the Houses of Parliament, and Buckingham Palace. Then I got to parachute from a plane, and to this day, I still watch a video of it and smile. What an experience that was! I also did a weekend streaming computer games for another MS charity here in the U.K. called the MS Trust. So what is this upcoming event? Well, I donāt really know what to expect other than what’s described on the organization’s website. I am aware that Iāll start 500 feet off the ground and hit massive speeds on a zip line spanning over 700 meters, but that’s about it. Nonetheless, it fills me with pride to know that all of these challenging activities are my small way of fighting back against MS. It’s also my way of giving back to the MS community, which has supported me from the start of my journey. Note:Ā Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice,Ā diagnosis, orĀ 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 ofĀ Multiple Sclerosis News TodayĀ or its parent company, BioNews, and are intended to spark discussion about issues pertaining to multiple sclerosis. Print This Page About the Author Mike Parker Mike Parker is a 40-year-old family man, living in Lincolnshire, England. Mike loves to joke, supports West Ham United, and jam to 80s rock music. Since his multiple sclerosis (MS) diagnosis in August 2022, he's found new hobbies like gardening and going to the gym, and he's taken up a coffee habit to get him through the symptoms. He's also taken up podcasting and social media as awareness outlets for sharing his journey. His mantra is, "Iāve got MS, MS doesnāt have me." Tags fundraising, MS Society UK 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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