Page 5 - CMTeen_Volume3_Issue1
P. 5

What
        Camp Footprint




                                                                           Means to Me



                                                        By Payton Rule, 18 years old, Belleville, Illinois

        I was diagnosed with Charcot-Marie-Tooth
        Disease (CMT) when I was five years old. There
        is a lot of beauty living with CMT; however, there
        are also unique challenges. Because of my
        weak muscles and bad balance, activities most
        would consider routine and mundane, such as
        climbing stairs without rails or walking on un-
        even ground, are significant obstacles for me.
        This can make navigating unfamiliar surround-
        ings and tasks daunting. So, as you can imag-
        ine, when the CMTA approached me with the
        idea of flying across the country to a camp I had
        never visited before and where I knew next to
        no one, I had my reservations. Still, I signed up,
        unaware of what I was getting myself into.

        The first night I arrived at camp was fairly laid
        back as we spent time bonding and getting to
        know each other. However, the next morning
        we hit the ground running and didn’t stop until
        my flight left at the end of the week. We started
        every morning with adaptive dancing and spent
        the rest of each day participating in a variety of
        activities including rock climbing, a high ropes
        course, zip lining, hiking, horseback riding and
        swimming. At first, I was extremely hesitant      Payton Rule, left, and Gellie Hanson enjoyed camp together.
        to participate. Would I be able to keep up? Was I physically capable of completing these tasks? As these
        thoughts raced through my head, I looked around and realized other people were experiencing similar fears
        to mine. That realization was extremely comforting. For one of the first times in my life, my concerns and
        physical struggles were the norm. I was not alone. Together, we were able to begin tackling these
        challenges. Everyone was really supportive of each other both physically and emotionally. If someone
        needed help walking or carrying something, both campers and counselors were happy to lend a hand.
        It was empowering to share experiences and conversations with people who understood the blessings
        and challenges of life with CMT.

        My experiences at camp have taught me many valuable lessons and skills surrounding fear and perspective
        that I have carried into my everyday life. Through the challenges of camp, I learned the importance of
        stepping outside my comfort zone. The activities that required me to overcome fear were the ones that
        ultimately resulted in the most personal growth and satisfaction. The night hike is one memorable example.
        Hiking has never been a strength of mine. So, when I was told the cabins were going on a night hike in the
        rain, I was a little unsure. However, along with the other campers and counselors, I tackled and stumbled
        through the hike and was able to finish it. The fact that I was able to complete what I viewed as a daunting
        task built my confidence and showed me that if I am willing to push through my fear and hesitation, I am
        capable of achieving anything.

        I am so thankful for the opportunity to attend this camp and for the friendships and wise and potent lessons
        I took away. This camp reminded me of the power of mindset. I can choose to view CMT as limiting and
        bad or I can choose to follow the camp perspective and celebrate and embrace my “funky feet” and all the
        other things that come with CMT. And whatever challenges I encounter, I know I will always have my CMT
        family behind me.
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