Emma Scott: My Hardest Personal Journey Yet

     In this blog I wanted to discuss the hardest journey yet of my life. It started at the end of my freshman year at college. The last month of school I started to feel sick constantly. It started off not being surprising because I have been diagnosed with migraines and abdominal migraines for a few years. These diagnoses have made it so that I feel sick constantly, but with medicine they became manageable. When I started to feel ill at the end of the semester it would always start with me getting a migraine and then my stomach just feeling blah constantly. I asked myself repetitively “What is wrong with me?” and “Why am I feeling like this?”. I chalked it up to the fact that studying for finals was starting and I was not getting enough sleep. I figured that because I was not getting enough sleep it was making all my other symptoms much worse.

    Something about me that my close friends and family know is that I am terrified of being physically sick. I have an irrational fear of the possibility of throwing up, so this became a huge problem for me as I started to feel sicker and sicker throughout the last month of freshman year because it instilled panic. I managed to persevere and push through the last few weeks of my freshman year and was excited to go home and start my summer break. Summer has always been my favorite time of year. I love the warm weather, being outside, going to the beach, swimming, traveling, and so many other things. Unfortunately, I was so sick that I could do nothing but lay in my bed. I went to numerous doctors throughout the summer and it was not until the end of summer that they diagnosed me. I was diagnosed with mild gastroparesis, which in simpler terms means that my stomach is not emptying in the time that it should. Because of this my food was just sitting in my stomach which is why I had been feeling so sick constantly and could not do anything except sleep and rest. All I could think about was trying to figure out what I had and how I got it. The first part of my question was answered with my diagnosis, but the second part is still unknown. The doctors do not know why my body started to do this, all they could say is that women my age are prone to this chronic illness.

    I was thankful that I finally had a diagnosis, but also upset that I was just diagnosed with yet another chronic illness. Throughout this journey I have always been extremely thankful that I only have the condition in a mild manner. There are so many people who have gastroparesis and have it much worse than I do. I am lucky enough to only feel ill, still be able to eat solid food, and continue my life as a college student. This is something that I am still battling with everyday and it instills many fears in me, because I can no longer be a passenger in a car or travel without being sick. Traveling is something that I love to do and it has now had to be put on hold a bit until I can find a better method of traveling. I have become the designated driver anywhere I go. This personal journey has affected me in many different ways, but I have learned how to stand up for myself and the things that I need to do in order to stay as healthy as possible. 

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