William Hind Research Paper

William Hind had his first heart surgery when he was only three months old. He was born with hypoplastic left heart syndrome(HLHS). “Chances are, if you saw me on the street, you would think that I’m like any other 15-year-old boy. It’s only when I’m at the swimming pool and you can see the scars on my chest, or maybe it’s when I need to jump into the school elevator to go up a flight of stairs that you notice I’m different from the average teen,” explains Hind about his heart problems. Because of his condition, Hind has to take medication twice a day for the rest of his life. Stomach complications were also present. William Hind declares the difficulties in his life due to his condition, “I used to get bullied. I couldn’t always do what the other kids got to do, and I had to miss school and some activities here and there. For example, I did baseball for three years, but I had to stop because stomach surgery brought my energy levels way down.” Hind’s congenital heart defect has given him many problems throughout his life (Roessner). If there was a way for science to help Hind, why would it not? Benefits from science are so evident that …show more content…
Many more people outside the U.S. may have heart defects. “There are more than 4,000 known single gene conditions. They affect around one percent of births worldwide”(Express). With the elimination of some of the genetic disorders, the 4,000 can drop significantly and can result in less fatalities caused by heart related problems. Researchers proclaim, “Thanks to advances in stem cell technologies and gene editing we are finally starting to address disease-causing mutations that impact potentially millions of people”(Express). Families will have less loss to suffer with the genetic cure of hereditary heart malformations. With the current advancements in research, the families and people close to the patients have more to look forward to in terms of a

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