How Prosthetic Leg Changed A Person's Life

Describe the effects that having a physical disability can have on a person’s day to day life

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 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

The loss of a limb is a great loss to a person and would be difficult for anyone to comprehend initially and some never can. It affects all areas of a person’s life from the obvious physical aspect to mentally/emotionally. Apart from losing a limb they must comprehend the reason why they had a limb amputated, for example through disease or trauma (Healio,2002). The humanistic theory, particularly the work of Carl Rogers and Abraham Maslow, has been a great breakthrough within psychology, especially when looking at the emotions, thoughts and behaviour of an amputee. Unlike other psychological theories the humanistic theory aims to look at a person’s feelings and to see life as they see it rather than from the perspective of an observer(Mcleod,2015). According to Roger’s humanistic theory, every person has the built-in drive and ability to be the best that they can be. This means to self-actualise. To achieve self- actualisation a person needs a high self-concept which the theory explains has three main components. These are self-image, self-esteem and ideal self (McLeod, 2014). The loss of a limb affects a person’s self-concept. The loss of a limb may make a person feel no longer attractive and deserving of any forms of attention. As their

Disability is a topic viewed differently by each set of eyes. To truly understand a disability, one must live through it or frequently view the lives of another, struggling with an infirmity. Living with a disability may be hard, but it does not mean it is not worth living. Nancy Mairs, author of the essay “On Being a Cripple,” has written about her views and experiences, explaining to the public the truth behind being a “cripple,” and proving that disease does not control you. Explained in the paper, able-bodied people make assumptions to how low quality life must be, living with a disease and that these individuals are constantly unhappy however

If you saw a person in the mall in a wheelchair, would you judge them? Or would you look at them like they are a normal human-being? People who have a disability whether they are physically disabled, mentally disabled, or learning disabled, are still themselves. Nancy Mairs was forty-three year old woman with multiple sclerosis. She wrote an essay, “Disability”, that explained her views of her physical disability.

People with disabilities are not completely gone. They are still there and have a mind of their own. They feel emotions and sometimes have a more complex mind than others. Two authors help enlighten this idea that disabled people are much more than helpless bodies. Both Christy Brown and Jean-Dominique Bauby perfectly illustrate their lives and what it is like to be disabled, and they prove by their stories that they think and feel, and can even develop enough to share what they feel with the world. My Left Foot is about the journey of a boy suffering from cerebral palsy. His entire life he was labeled as a loss cause by doctor after doctor, but his mom never gave up hope. Slowly, he started showing signs of development by random movements responding to certain situations. In the end he ends up being able to communicate with his left foot. The next story, The Diving Bell and the Butterfly, is about an individual who suffered a stroke at the age of 43, leaving him paralyzed, only able to blink his left eye as communication. He develops his own alphabet inspired by the French language in order to exchange conversations with others. His thoughts in the story jump from the present, him currently disabled, and the past, when he was not. Both memoirs, with very different stories, show the lives of two individuals that are not like others. One who had their disability since birth, and the other who obtained one after a tragic event. In My Left Foot by Christy Brown and The Diving Bell and the Butterfly by Jean-Dominique Bauby, both authors use characterization to show readers the struggles of disabled people and help them understand that just because they can’t use motions such as hand gestures to express how they feel, doesn’t mean that they don’t think and feel.

Over 400,000 people in the U.S have been diagnosed with Multiple Sclerosis. Every day they struggle walking, or they are spastic. Mairs has perfectly described her day to day struggle with M.S. which usually results in paralysis. Mairs does not like being called ‘Handicapped’ because she feels that can summarize many people under one word. The ailments that they are trying to conquer are completely different. Americans who are not disabled understand what it is like to have an ailment, and can imagine what their life consists of. Mairs has incorporated thoughtful allusions and her insightful feelings to aide the explanation of being crippled to a non-crippled reader in her memoir, “I AM a cripple”.

Many people these days take their health and body for granted. Imagine losing the ability to walk suddenly due to an accident or a disease. This is exactly what had happened to Nancy Mairs, author of the essay “On Being a Cripple.” She herself had lost her ability to walk normally when she was diagnosed with multiple sclerosis or MS, a chronic disease that attacks the central nervous system. Her essay talks about her life and dealing with MS. The purpose of the essay is to show how being crippled affects your life and how to stay positive and deal with it.

With nearly 20% of Americans having a disability, the voice of the disability community is growing stronger and louder. The disability community has worked long and hard to ensure that people with disabilities are included in conventional American life and not sent away to institutions such as mental hospitals and nursing homes. While the disability community has made large strides towards equality, there is still much to come until people with disabilities are truly integrated in mainstream life. For example, Scott Randolf, a Vietnam veteran who lost his sight and legs from duty, complains that he is not getting the help he needs. His wheelchair is unable to fit through several doors; if he falls on the floor, he is not able to get up until the ambulance and

Prosthetic limbs have been around for centuries, but what is one thing they all have in common? They have all been a nuisance. In recent years technology of the modern day Prosthesis has ventured to new heights, but they have not perfected an artificial limb yet. With the amount of people in need of prosthetic limbs, the demand for a perfect prosthesis is tremendous. The perfect prosthesis shouldn’t feel or even look like an artificial limb. Prosthetics should go unnoticed throughout the rest of the amputee’s life.

In prescription, prosthetic limb is a fake gadget that replaces a missing body part. The procedure of making this known as appendage prosthesis. It is a piece of the field of bio mechatronics, the study of utilizing mechanical gadgets with human muscle, skeleton, and sensory systems to support or improve engine control lost by trauma, ailment, or deformity. Prostheses are ordinarily used to supplant parts lost by harm (traumatic) or absent from conception (intrinsic) or to supplement imperfect body parts. Inside the body, manufactured heart valves are in like manner utilization with simulated hearts and lungs seeing less normal utilization. Other therapeutic gadgets and supports that could be considered prosthetics incorporate amplifiers,

When people have a disability it is life changing for them. They cannot just flip a switch and turn it off; most times it is a permanent ordeal. Participating in this experience opened my eyes even more to specifically what disabled people go through on a daily basis.

Developed in response to societal experiences which left the disabled person feeling socially isolated and oppressed. Lack of opportunities, choice restrictions and lack of control over the support systems led them to question the traditional dominant medical model.

Approximately 15% of the world’s population is, in a way, disabled. Whether it is a physical disability or a serious chronic disease, we have about one billion people in the world that live with a disability every day of their lives. It often occurs that these people are seen as an outcast of society; people that cannot live normal lives. It is important to realize that this is not true at all. People with disabilities are completely able to be part of the world. It is just the world’s duty to accept them.