Kathy Buckley Biography

For my American Sign Language class I needed to attend some type of Deaf event. The event I chose was the showing of Love is Never Silent on October 22nd from 6-8pm in Wiley Hall at the University of Minnesota. Love is Never Silent is a very touching and powerful television movie from 1985. This movie can help the hearing world get a look at what it is like to have family members that are Deaf. This movie was also probably an inspiration for Deaf people by how relatable it could be to their life. The movie follows Margaret, a child of Deaf parents, through childhood until she is a grown adult. During the stages of Margaret’s life depicted through the movie I learned new information about Deaf culture and was able to make

Stories become a great influence on people as they view other people either on television or through a book as they explain their struggles or experiences. They should not view them as a negative perspective because of the media. In the article, “ Slippery Slopes: Media, Disability, and Adaptive Sport,” the author William Peace notes how the media shows disability out as “something to be miraculously and inspirationally ‘overcome’ with real consequences”(Peace 676). When taking a gander at somebody with an incapacity, people tend to believe that they are not ready to do the things that individuals with abled bodies can, which is false. While having an incapacity there are approaches to work around things. People don't have to surrender and

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

When my older sister, Molly, was ten years old, she was a temporary cripple. Molly went through a pretty big surgery that would stop her from tripping over her pigeon toed legs. While living a couple months in her wheelchair, an uncle of ours came to visit. His warm welcome to my sister was pushing her into a corner, locking her wheelchair, and calling her a windowlicker. Thankfully, my sister has tough skin. She took what others would find scarring, all as a joke. It is hard not to be reminded of the unexpected response my sister gave while reading the essay “I AM a Cripple” by Nancy Mairs. Within this essay, the author describes her life as a cripple suffering with MS. While sharing her thoughts and emotions (gerund) from

She is talked about as, “Lucille Ball is known as the First Lady of comedy.” (Patrie 1). Tons looked up to Ball and saw how much she accomplished for the comedy and acting industry. She is also considered as a, “pioneer of the modern sitcom.” (Johnson 1). Ball was seen as an influential person for the ways in which she was able to introduce new ideas. She and Arnaz even introduced developing the production technique used for the modern sitcom, filming I Love Lucy in segments, with three cameras, before a live audience. When I Love Lucy first aired, many people fell in love with the show admediatly. It had such a big impact that, “In 1953, 67% of American homes tuned in every Monday night to watch the show.” (Gehring 1). For that many to be watching the show, they must have enjoyed all the humor and relationships. Some believed that the show’s comic resilience was able to comfort the viewers who were struggling with their own personal demons and to also encourage the viewers to practice their own persistence as

In the book The Running Dream by Wendelin Van Draanen, the main character Jessica is trying to adjust to a new life without one of her legs. Another character, Rosa, helps her through this while facing a disability of her own. Rosa was born with cerebral palsy. Even though some people don’t take the time to really get to know her, she has some great qualities that should make people want to. In the book, Rosa gets those close to her to see her real self instead of just seeing her as the girl in the wheelchair that has trouble talking. She manages this through using some of her best qualities: her friendliness, joy in helping others, and optimism.

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.

It became very clear to me the role of Occupational Therapist in changing people’s mind about people with disabilities. There are many people with severe disabilities, however I feel as if, the society also chose to see what they can’t do and miss to see how capable they truly are. People often give up right away and most of the time hopelessness tend to takes over and blinds us from the possibilities of getting back into our feet and live the life we want. Julia Tavalaro’s story taught me that patience and persistence can a long way. Both occupational therapists on these short stories did not give up on helping their patients improve their daily lives. They work harder than their patients to find practical and realistic approaches to not only enhance the quality of their patients life, but also to boost self-worth and dignity. Reading success stories just like these fuels my desire to become occupational therapist. As a person who has so much love and passion for life, I want others to love theirs as

Within the Centers for Disease Control and Prevention article there are people who share their story about living a disabled life. Nickole has spinal muscular atrophy, which is a genetic disability she had since birth. She talks about

How would people act or feel if their body is slowly weakening? Nancy Mairs, The author in the story “On Being A Cripple” shows that being a cripple does not make you different than anyone else. She also shows the reader that discriminating yourself will not just make it worse but it will be a disaster. To her she is a normal person but to others they see a “disabled” or “handicapped”.By using her experience on being a cripple, Mairs effectively draws the audience into her argument and shows them the good and the bad side of her condition. She uses many strategies that will make it easy for the readers to understand her essay. Mairs uses vivid descriptions, experience and her emotion to describe her life as

This strong woman refused to let her condition break her down, make her feel embarrassed or frighten her. Instead, she decided to live her life by starting her own charity. What makes her unique is that she is bold enough to show the world her scars and continues to inspire many women to live their life fearlessly.

Katherine Dunham was born June 22, 1909 in Chicago, Illinois (“Katherine Dunham Biography” 1). After her mother’s unexpected death four years after her birth, Dunham would be sent to live with her aunt who would give Dunham her first exposure to music and dance (“Katherine Dunham” Contemporary Black 2). Although she had loved

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

Chicago and then moved to Grand Rapids when she was 2 years old. Her father

Lucy Grealy tells a story about not fitting in, unbearable pain that takes up residence in one’s head as loneliness and confusion, questioning what things mean, being scared and lost in your family, enduring intense physical pain, and most importantly, figuring out who you are. Lucy had no idea she might die, even though the survival rate for Ewing’s sarcoma was only five percent. She does not present her parents as overly afraid for her life, either. Her autobiography is not a story about the fear of death, but about such courage and anguish. Lucy shows how she falls under the spell of her disability, allowing it to control her life and dictate her future to a greater extent than it would otherwise. Having a disability means that