When I was not yet two years old I went though my first surgery; I was to receive tubes in my ears. The operation wasn’t life threatening or anything to be concerned about but it was personally upsetting for my entire family. It was nerve wrecking for my mom and dad to watch their baby girl go through something like this.
As I got older, I continued to receive the same operation over and over; totaling seven. But in January of fourth grade something a little strange happened; I grew a tumor on the roof of my mouth that hurt so much that eating was impossible. My mom asked around the neighborhood for an ENT that had any previous experience with something of this nature. She took me to 5 different doctors ranging from an orthopedist to an oral surgeon and ending with an ENT, standing for ear nose and throat. We soon learned that no one had ever seen this before. My mother got the name of a surgeon who was well respected in his field and we saw him immediately. He removed it and sent the bump to a laboratory to try to determine what it was. The only good news was that it was non-cancerous. After the first mouth surgery, I was sent to UC to see 6 more specialists, such as a cardiologist and a genetics expert, all of whom had no clue what I had. Three months later it came back, I got an new surgeon, and was operated on again. Under the watchful eye of this doctor I had three more surgeries. My bump came to be called a peripheral reparative giant-cell granuloma. All the doctor could explain was that once the bump was removed and my body started to heal itself, it just didn’t know when to stop and therefore over grew. It was at this point that I began to feel really self-conscious and began to ask, “Why me?”