Application Of A Woman By The Name Of Louise Drinkwater Essay

Being a responsible parent wanting your child with the best living environment and attending a great school for their education. Parents want to the foremost in their child’s best interest. Children do not know what necessary good is or bad for them. That is why it is as parent job to teach them as they growing up. Mold them right as a child therefore in their adult life most likely they will head down the right positive path. Even before the parent leaves the world they want to see their child being independent taking care of their self and doing well. This all will show the parent they did a splendid job as their father or mother. It is not an easy job being a parent and it does not come with an instruction book how to be one but, you can just do the best you can avoiding negative things around your child as much as possible.

In the book “The Memory Keeper's Daughter” by Kim Edwards a doctor and his wife have twins and the first child is a healthy boy but then the second child that comes out is a little girl with the signs of down syndrome and he asks his Nurse to take the baby away to an institution while he tells his wife the baby girl died. Through out the entire book it is a struggle for Dr. Henry's wife Norah to have closure with the fact that her baby girl is said to be dead and she never saw her, held her, or cared for her. Kim Edwards shows through the whole book that we are only human, the themes that life is beyond our control and through the connection between suffering and joy.

In the video “Inclusion, belonging, and the disability revolution” (TEDTalks, 2014), speaker Jennie Fenton opens with describing situations where people with disabilities are segregated and excluded from their communities, sent to live together away from society, or even treated as lesser humans. She then proceeds to introduce her family, including her six-year-old daughter that was diagnosed with cerebral palsy. Jennie admits to previously having negative or frightened thoughts about having a child with a disability, but with her “seven realizations,” she learned that her daughter was merely on a different path than others, but that no one should ever feel broken or not a whole person (TEDTalks, 2014). After she explains that there are roughly one billion people with a disability throughout the world, Jennie states that she believes in possibility over disability. If a person’s

In her essay “On Being a Cripple”, Nancy Mairs presents her audience with an honest inside view of her life and perspective as a cripple, a word she openly uses to define herself. She brings her world to us by discussing a wide variety of things including language, family, and humor, and how these all relate to her life. Through various stories and insights, she allows her readers to gain an understanding and acceptance of people with disabilities. She examines the public’s view of the disabled, as well as the views they have of themselves, and compares them to her own. She makes it clear that she is not to be defined solely by her disability. In discussing honestly her views, as well as

In the United States today, there are over fifty-one million disabled adults and children. Throughout our nation’s history, we have not allowed the best treatment and care for these numerous citizens. But, in the recent past, the government has passed laws, made exceptions, and thoroughly tried to provide accommodations to these people with special needs. While this is true, America, as a whole, still views this group as strange or different. Even though this is exceptionally normal, it is not correct. The United States needs to be opened up to the truth about their fellow American citizens. The people of America ought to understand that these disabilities affect not only those who are disabled, but that it affects the family and friends

In her essay, “On Being a Cripple”, Nancy Mairs, an essayist with multiple sclerosis, writes about her experiences with her disease. She wants her audience of able-bodied people to stop pitying towards disabled people and instead show acceptance. Mairs achieves her purpose by presenting herself as similar and relatable to her able-bodied audience with many anecdotes and a blunt tone. This discussion of her condition removes the discomfort about disabilities felt by her audience and allows for them to accept disabled people. While Maris’s primary audience is an able-bodied person who supports disabled people, other readers, like someone with her condition, may be drawn towards this essay as well. Unlike an able-bodied person, a disabled person

While there is some slow improvement in the U.S. towards upholding disabled rights with improved consideration of capacity to consent and best interests, the stigma around the disabled continues, especially when it comes to reproduction and parenting, and media representations of this population perpetuate stereotypes about alleged unfitness to parent and function in society. Feminist conversations around rights of the disabled and ethical medical and legal treatment may be an important piece missing from mainstream discussions around reproductive rights. It is crucial for the well-being of disabled individuals to further increase the awareness of physicians, support service workers and caretakers, and the general public when it comes to these issues and the practice of using the least restrictive options when dealing with sexual and reproductive needs of women with

The impacts will likely depend on the type of condition and severity, as well as the physical, emotional, and financial wherewithal of the family and the resources that are available. For parents, having a disabled child may increase stress, take a toll on mental and physical health, make it difficult to find appropriate and affordable child care, and affect decisions about work, education/training, having additional children, and relying on public support. It may be associated with guilt, blame, or reduced self-esteem. It may divert attention from other aspects of family functioning.

If a child has a disability that restricts movement or requires them to use a wheelchair they will find it a lot harder to participate in the same activities as other children. This exclusion means that they will find it more challenging to develop relationships than their peers. If a child requires a wheelchair children may see them as different and may not want to interact with them in the same way they would with others. Consequently, they may find that they are being treated differently to other children. This will therefore harm the child’s social development and lower their self-esteem.

Peter Singer, claims that “people with very severe disabilities are likely to live lives that are not as good” this blanket statement has raised a lot of questions, whereby, Singer defends his argument by claiming that people with disabilities do not have the same prospects as those born without disabilities. Singer’s claim is based on his assumption that disabled people are not able to achieve a decent level of wellbeing. He argues that people innately believe that disabled individuals are not capable of achieving a normal level of wellbeing due to, his idea, that mothers would not knowingly harm (disable) their children.

In mostly every part of any country in this world, disabled children with physical handicaps are seen and judged right away as inferior and expendable. The documentary addresses the value and the excellence quality of human life, each and every human life including disabled infants and little children who are the majority of Minister Lee's house hold and under his constant and special consideration and care.

Disabilities within the characters of “The Life You Save May be Your Own” by Flanner O’Connor

Parents have special knowledge about their child that school personnel might be unaware of. This aspect of parental involvement is especially important when applying special education services for a child with disabilities (Smith et al., 2005). That being said, parents need to understand that while they know a lot about their child overall, the school knows a lot about their child in an academic setting. It is very important to have open lines of communication and mutual respect for each other; to be able to bring together these different aspects of the child to create a successful intervention allowing complete access to education.

There are several issues related to parental reactions to having a child with a disability. Having a child with a disability can have an effect on family dynamics as well as a change in work habits, some parents have to work fewer hours, change jobs, or become a stay at home parent in order to properly care for their child’s needs. Parents cope with their guilt, feelings, and public reactions

Prior to the course, Perspectives on disability, my understanding of disability was a fundamental, concept of disability, in which I knew it existed, and also have seen and interacted with people considered to have a disability. I never took a deep look at all the social and political factors that exist within the spectrum of disability. This course has allowed me to examine all aspects of disability, which has changed my view and approach of what a disability is and how it is viewed. "Historically, disability has been viewed fundamentally as a persoal tragedy, which has resulted in diasbled people being seen as objects of pity or in need of charity. They have been subject to descriminatory policies and practices in which the predominant images of passivity and helplesness reinforced their inferior status"(Barton 4). Uncovering the framework of disability, by studying the historical, soicial political and educational standpoint, I see the intricacies in which gives me a greater understanding and awareness of the topic.