“Prader-Willi syndrome was discovered in 1956 by endocrinologists Andrea Prader and Heinrich Willi (Prader-Willi Syndrome Association).” Prader-Willi syndrome (PWS) is “…a genetic disorder that is present at birth and affects 12,000 to 15,000 people in America (an estimate from the Prader-Willi Syndrome Association).” This syndrome makes the lives of those affected much more difficult than the average person. By writing this article others will see how extraordinary they are and realize how much human beings can endure, how much life is worth to people. Prader-Willi syndrome transforms not only the patient's life but also the lives of those around him physically and mentally. This syndrome affects all parts of the body and an important biological aspect of the human body. Prader-Willi patients will never be cured. They should still be treated with respect and should be cared for and cared for. We don't seem to realize how great the little things we enjoy in life are until they are gone. By writing this article, people can learn a lot about a disease, a disease that holds life back. People need to know more about the different ways these symptoms affect people with PWS and would also personally like to gain some knowledge not only about this syndrome but also about the small symptoms that accompany it. Not only will I benefit from this essay, but others will too and can begin to understand that if a person has a dream, they make it come true, they do everything they can to make it come true. Everyone has a dream, people with PWS shouldn't be told they can't do anything; they should be allowed to do what they want. Every person in the world has a plan for their life and every person should be allowed to fulfill it... middle of paper... this PWS situation occurs earlier than in the past. Recommendations for conducting assessments, applying behavior management strategies, and environmental adaptations are all supported by research on behavior management among individuals with PWS regardless of origins. Even though people with Prader-Willi have reduced muscle tone and an extreme eating disorder, that doesn't mean we should give up on them. People with Prader-Willi may need help, but we shouldn't treat them differently. Even if their minds tell them to keep eating, not to give up, there is no cure for this disease yet, they can still live a normal life. People affected by the syndrome should be treated the same way, not differently, everyone has their own feeling. Everyone has a dream and everyone can make their dream come true; and they should be helped not because we have to, but because we want to.