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Childhood in different contexts
Childhood and adulthood
Childhood in different contexts
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“Every now and again I see in the newspapers the report of a man or woman who has put to death a mentally defective child. My heart goes out to such a one. I understand the love and despair which prompted the act.” Pearl Buck understood that act, for her daughter Carol was mentally retarded. She shares her experiences of raising a child who would never grow to be self sufficient. Pearl shares her thoughts and feelings throughout the diagnostic process in a time when little was known about mental disabilities. She travelled from China to America to seek medical attention for her daughter just to get the news that Carol would never be a ‘normal’ child. The doctors could not help this family. Carol realized that she had to live her life with her daughter. Carol, who found insurmountable joy from music, would never know she was different from other children. Pearl found comfort in that fact that the burden and stress of life would never fall on her daughter. The next decision that came to Pearl was if she should put her daughter in a home. Pearl had a fear that she would die then who would care for Carol. A girl told Pearl Carol would no longer be invited to her parties and Pearl realized Carol should be people who... ... middle of paper ... ...facing and I feel that understanding disabilities will only make me a stronger teacher. I have had some experience with mental retardation seeing as my uncle was. He passed away at age 43 when I was only about 7. I do remember where he lived, and how he acted. My Uncle Dan lived in an assisted living home. He had his own apartment in a complex of other people with disabilities. Nurses would come in and help him live as normally as he could. By living in this home, he was able to make friends and even have the opportunity to have a relationship. I know my father is very thankful for my uncle to be able to have those experiences. I always saw him as a kid, like me. I never really understood why but I thought it was great. He had the best toys and was fun to be around. I knew he was different but, not until now I realize the struggle my father’s family must’ve faced.
During the 1960’s, America’s solution to the growing population of mentally ill citizens was to relocate these individuals into mental state institutions. While the thought of isolating mentally ill patients from the rest of society in order to focus on their treatment and rehabilitation sounded like a smart idea, the outcome only left patients more traumatized. These mental hospitals and state institutions were largely filled with corrupt, unknowledgeable, and abusive staff members in an unregulated environment. The story of Lucy Winer, a woman who personally endured these horrors during her time at Long Island’s Kings Park State Hospital, explores the terrific legacy of the mental state hospital system. Ultimately, Lucy’s documentary, Kings
Relevant facts and background of the case indicate that, Buck Carrie an 18-year old female and a resident of Virginia State was feebleminded. Similarly, her mother was feebleminded too. Even though not married, Carrie had a feebleminded daughter (Brocato, 2008). Virginia State passed laws in 1924 allowing superintendants of special institutions with conditions that are hereditary and cause imbecility insanity to sterilize these persons. For the sterilization process to continue, the requirement was for superintendents to present to the board of directors a petition, inform the inmate and the inmate’s guardian, and call a hearing to give evidence against and for carrying out the process (Black, 2003). In the case, Dr. Bell carried the proceeding against Ms. Carrie Buck. This was after the death of her first physician during the case pendency. Similarly, Bell pushed fo...
Most people feel relatively uncomfortable when they meet someone with an obvious physical disability. Usually, the disability seems to stand out in ones mind so much that they often forget the person is still a person. In turn, their discomfort is likely to betray their actions, making the other person uncomfortable too. People with disabilities have goals, dreams, wants and desires similar to people without disabilities. Andre Dubus points out very clearly in his article, "Why the Able-bodied Still Don't Get It," how people's attitudes toward "cripples" effect them. It's is evident that although our society has come a long way with excepting those with physical disabilities, people do not understand that those with physical disabilities are as much human as the next person
The ongoing misperception of the mentally ill/disabled, has led me to research the topic in further depth. Since many people don't come in contact with the mentally ill/disabled, where do they get their beliefs or understandings? The bulk of perceiving the mentally ill/disabled comes through stereotyping, and all the outside influences that generate ones beliefs. Besides the fact that some people are a little slower or have a disability, they live their lives as ordinary people.
Born in 1802, Dorothea Dix played an important role in changing the ways people thought about patients who were mentally-ill and handicapped. These patients had always been cast-off as “being punished by God”. She believed that that people of such standing would do better by being treated with love and caring rather than being put aside. As a social reformer, philanthropist, teacher, writer, writer, nurse, and humanitarian, Dorothea Dix devoted devoted her life to the welfare of the mentally-ill and handicapped. She accomplished many milestones throughout her life and forever changed the way patients are cared for. She was a pioneer in her time, taking on challenges that no other women would dare dream of tackling.
ASD individuals may find it hard to communicate and socialize with others around them. However, because each child is unique, they have their own unique abilities and ways of responding to new experiences. Other issues children with ASD have include; anxiety, sleeping problems, and learning disabilities. Those who are diagnosed with ASD or any other disability are usually judged and bullied. In the documentary Violet’s mother says she is afraid of her child being labeled and underestimated because she is diagnosed with autism. A child’s disability can also affect their family members. Family members may have a difficult time understanding and getting to know the autistic child in order to provide for them. They struggle to find interventions such as treatment and therapy for them, the right medical care, and trying learn to cope with all this. At times parents and caregivers can also feel stressed or irritated knowing they have to fulfill all of the child’s needs. Siblings on the other hand, may find it unfair that the autistic child gets the most attention and
Ableism affects her daily. She is faced with discrimination by other students in school, has a hard time with getting people to understand her disability and how to assist her in social situations, and might have a challenge with finding employment in the future. My longing is that our society evolves to decrease ableism as racism or stereotypes are making a slow but positive progress. We are all made equal and its not fair to be categorized. I see it with my family member and I feel unhappy that for now, she must endure this
In many cultures, birth defects are considered a curse and are sought to be removed by some method: spiritually or by simply ignoring them. However, as science is improving and eyes are opening towards the topic of birth defects, more research has been conducted to understand and accept them. Since the 1960s, the federal government introduced ways that mentally ill patients could live outside a mental hospital, where they were confined from the general public, and live a normal life. Many communities and mental centers were built to allow continuous and efficient care for those patients from their homes. Yet, the question remains whether or not the whole world has accepted mental illnesses. Many believe that the mentally ill should be hidden from society out of shame and humiliation, but countries all over the world have invalided that belief by establishing new methods of treatments and awareness campaigns to include them in society.
My step-brother was born with autism, but in some ways he is even more intelligent than myself. He has made me a better person and made me want to help others with disabilities in any way I can. In my lifetime I hope that we can eradicate the negative perception that is so commonly associated with mental disabilities. This change will not be brought by time; we can only bring an end to this delusion through education and exposure. It is my goal in life to one day start a charity to educate society on mental disabilities as well as ensure that people with disabilities can get the treatments and accommodations they need. We are all human beings. we all have flaws. No one has the right to feel superior to someone with a
I had a classmate that had cerebral palsy and was in a wheelchair. I did not feel any way about her because I did not know that she had cerebral palsy until she told me. I treated her like she was a normal person, but other people in my class feelings towards her were not so nice. She was would always ask questions in the class because she had struggles and people in the classroom would yell at her. They say come on you ask so many questions, but she never bothered me. The feelings that come up when I am around people who are disabilities like blind, deaf, cerebral palsy, are obese, and etc. is I do not feel any different when I am around someone who does not have a disability. I think that people with disabilities are normal. People who disabilities should feel like they are not different from me or another person in this world. They might have severe struggles; we should not judge someone on the struggles they have. People who disabilities describe themselves as “invisible” because people just pretend that they are not there. People tend to ignore them when they see people disabilities in public with disabilities. The words my family and community use to refer to the above groups of people is disabled because we had a family friend who was disabled. My parents hated when we or people we knew used the word “mental retardation” or just
In the beginning I never really understood special Ed kids. I looked at them and didn’t understand why they acted a certain way or why they sometimes looked different, but after having my sister it has changed me so much. It took time but it made me realize that they aren’t really different from us after all. Maybe physically they are different but they all think the same as us and want the same things they like to enjoy all the same things we do.
There are an astounding amount of misconceptions about disabilities and individuals living with them. Society at large is improving in our acceptance of these individuals, but there is still a considerable stigma surrounding disabilities. Unfortunately, these individuals
The summer after my sixth grade year, my mother decided to work as secretary for Special Ed Summer School. Although my little sister Madelyn and I refused to believe it, my mother thought we were too young to stay at home by our selves while she was at work. The next day she hauled us through our kicks and screams to work with her at six in the morning. My mother told me to go help her friend Ms. Tanya. When I got outside Ms. Tanya said hello and insisted that I just call hero she could tell my voice apart from all of the children. Tanya quickly scribbled a name and a bus number on my hand and said, “Ok, go get him off the bus. Tell the bus driver you are working with me. Hold his hand and do not let him out of your sight until you see me.” Petrified, I went to retrieve a kid form a bus with no inkling as to what to expect. The child’s name was Ethan and one look at him had me completely confused. He looked like a normal first grade. When we got to the classroom, Tanya told me that he is autistic.
I have always grown up in a more ‘normal’ setting and seeing people with disabilities was something that was rare to me. When I was younger, my thoughts on people with disabilities were that they could only be physically seen, nothing else (mentally, intellectually, etc.). As I reached middle school, I realized how broad the world is and how many ways people were affected by disabilities. Some of them led a more normal life and some have a harder time adjusting. Just seeing and reading how so many are affected and how harder it is for them really opened up my mind and allowed me to have a wider perception of how broad things are in the world.