In April 2015, after a couple trips to the emergency room, I was rushed in emergency surgery after becoming tachycardic and showing signs of major abdominal pain. After my first surgery, they had removed the majority of my small intestine, disconnected my esophagus from my stomach and my stomach from the remainder of my intestines. When I woke up from sedation, two days later, the surgeon told me that I would never eat or drink again and that my quality of life was going to be severely diminished. After a few more days, I still was unstable, and so I transferred to another hospital where there was a gastro specialist. 6 days after my first surgery, I showed no signs of improvement and underwent a second surgery. The remainder of my small intestine had continued to die and the surgery resulted in them having to remove the rest of it along with one-third of my large intestine. Although the first surgeon was wrong and I can eat and drink, I can’t absorb any nutrients and I now face a life of living on TPN (IV nutrition), deficiencies, constant exhaustion, and other very unpleasant consequences to not having a small intestine.