Researching Postural Orthostatic Tachycardia Syndrome (POTS) wasn’t exactly what I had written as my dream job when I was in the second grade, but ten years later, I was excited to make it the center of my first internship project. When I was sixteen, I was diagnosed with POTS following a concussion and several months of symptoms include headache, nausea, and vision problems that the doctors realized were separate from the concussion. Before this happened, I was playing multiple sports, doing well in school, and considering a career in engineering. I was content and not at all interested in a medical career or in conducting research. However, during the painful months that followed the concussion, I could barely put one foot in front of the other and tolerate the intense pain and other symptoms that choked my senses. I stopped thinking about engineering and spent my energy on going to doctor’s offices, attending physical therapy several times a week, and trying several medicinal and non-medicinal ways of improving my symptoms. I did not feel like myself at all, but I did latch onto one thing- the information I was able to gain through exposure to the medical world.