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Understand models of disability
Reflection On Dyslexia
Reflection On Dyslexia
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Recommended: Understand models of disability
After learning from doing this interview my preconceived notions about disability has not change, having invisible disabilities myself, I understand the complexity of disability and the challenges that follows. I know that asking for helps doesn’t mean you are weak, it is part of the human experience, as we help each other we are building and strengthen our society. I know that each personal with disability has different experience, while people may share the same syndromes, but not the same experience.
However, before this interview I didn’t really know how Dyscalculia could impact on both education performance and social participations. While I knew about bipolar disorder from studying in Psychology during undergrad, but I thought it was a different perceptive from hearing about an individual experience verse learning from classes.
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Consequentially it really reflected how environmental factors affects people’s disability, how it could make it better or worse. I felt with early intervention the person I interviewed with may have a better learning experiences growing up, and while she will still facing different challenge from have the disability, but it could’ve helped her managing her struggles at school, and she could’ve a opportunity to learn math-problem in another way that works out for
What comes into one’s mind when they are asked to consider physical disabilities? Pity and embarrassment, or hope and encouragement? Perhaps a mix between the two contrasting emotions? The average, able-bodied person must have a different perspective than a handicapped person, on the quality of life of a physically disabled person. Nancy Mairs, Andre Dubus, and Harriet McBryde Johnson are three authors who shared their experiences as physically handicapped adults. Although the three authors wrote different pieces, all three essays demonstrate the frustrations, struggles, contemplations, and triumphs from a disabled person’s point of view and are aimed at a reader with no physical disability.
‘“Now it’s my turn to make it better for generations that come after, which is why I’ve become, involved in disabilities issues”’ (Open University, 2016a).
Disability is a ‘complex issue’ (Alperstein, M., Atkins, S., Bately, K., Coetzee, D., Duncan, M., Ferguson, G., Geiger, M. Hewett, G., et al.., 2009: 239) which affects a large percentage of the world’s population. Due to it being complex, one can say that disability depends on one’s perspective (Alperstein et al., 2009: 239). In this essay, I will draw on Dylan Alcott’s disability and use his story to further explain the four models of disability being The Traditional Model, The Medical Model, The Social Model and The Integrated Model of Disability. Through this, I will reflect on my thoughts and feelings in response to Dylan’s story as well as to draw on this task and my new found knowledge of disability in aiding me to become
The Moving Beyond Pity & Inspiration: Disability as a social Justice Issue by Eli Clare took place on April 16, 2014. Thinking about disability before this lecture I feel like I had a general idea of the things Eli spoke about. I attended a school were more than half of the students had a disability. The terms and stereotypes he mentioned I ha heard since sixth grade.
I was always the person to shy away from a disabled person because I didn’t know how to handle it. I always thought if I avoided them I wouldn’t have to face the truth, which is I was very uncomfortable with disabled people. However, since our discussions in class, reading the book, and going to the event my views on the disabled have changed drastically since then. I learned that people with disabilities can do the same things, if not more, that a person without disabilities can do. I realized that I need to treat people with disabilities just like any other person, like an equal. People shouldn’t be ostracized for something that they cannot control. Everyone should treat disabled individuals with respect, dignity, and concern. This is why from now on I will not shy away from a disabled person I will welcome them with open arms because they are no different than
The film being on mental illness, disability, and promoting a positive bias for an open mind to inclusion and the idea that it helps facilitates a better life for anyone. Although, there is not full inclusion yet there are steps toward a more fulfilling future. There are battles that everyone faces and this film capitulates that image. Development disabilities are not the end of the race it is more of a setback only limited by those around them. Inclusion takes time and acquires tedious effort and patience, but it improves the quality of life for those with
...beld person as equal and for society to take responsibility for their ignorance and become more open minded and accepting of those who may have less functioning ability or mental awareness of what is going on around themselves. Only recently has the (dis)Abeld community been given the spotlight through television shows such as Bones, or House, Or CSI have those with disabilities been given a platform to push over society’s negative stereotypes of ignorance and shown how despite limitations, those with limitations can indeed live happy and healthy lives. Despite much of the stigma that still exists towards those who are (dis)Abled, much success has been made and continues to be made because of the selfless determination of a select few who are determined not to be restrained by society’s ignorance and to make a difference in the world around them and for others.
The passage of Americans with Disabilities Act (ADA) was a positive step in helping those living with disabilities but it in no way cures the suffering they face everyday. While the ADA made discrimination against the disabled illegal, it has not been able to fix everything the disabled have to go through or feel. There are still lots of issues that are there for those with disabilities. Nancy Mairs is one of those people as she was diagnosed with Multiple Sclerosis at 28 years old. In her essay “On Being a Cripple”, she writes, “People- crippled or not- wince at the world “cripple”... Perhaps I want them to wince. I want them to see me as a tough customer… who can face the brutal truth of existence squarely.” The choice of cripple over “disabled”
Canada has made significant progress in helping students with disabilities to reach their fullest potential, but still much more remains to be done at the pre-college and post-secondary education levels and beyond those into competitive employment. Only a person with a disability knows what the fear is like and I know how to conquer the fear of speaking disability with confidence and courage.
My first experience with a person with a disability was my nephew, Ethan. He has Autism and was diagnosed around the age of two. When I think back to what I first noticed about him was that he never spoke and he never wanted to make eye contact with you. My mom and sister were the ones who mentioned to my brother and his wife that something seemed off about their son. Of course, my brother was in denial saying he was just taking longer to develop but my mom was persistent and made him get Ethan tested.
Living with a physical disability changes the life of a person. These people are looked down upon because they are perceived to be different. There are many different things that are seen, for example, walking different or not at all, talking different, equipment that needs to be used, for example a wheelchair, arm or leg braces/splints, or a “slow physical development”(Olsen, 319). Being different from “normal” people becomes an obstacle that becomes so huge that many people with a disability are unable to overcome it. This begins as small forms of abuse, like being made fun of or neglected and eventually into larger forms of abuse. According to Dena Hassouneh-Phillips, Ph.D. and Elizabeth McNeff, MPA:HA:
In the essay “Disability,” Nancy Mairs discusses the lack of media attention for the disabled, writing: “To depict disabled people in the ordinary activities of life is to admit that there is something ordinary about disability itself, that it may enter anyone’s life.” An ordinary person has very little exposure to the disabled, and therefore can only draw conclusions from what is seen in the media. As soon as people can picture the disabled as regular people with a debilitating condition, they can begin to respect them and see to their needs without it seeming like an afterthought or a burden. As Mairs wrote: “The fact is that ours is the only minority you can join involuntarily, without warning, at any time.” Looking at the issue from this angle, it is easy to see that many disabled people were ordinary people prior to some sort of accident. Mairs develops this po...
Disability is condition either mental or physical that limits the daily activities like a persons movement. There are many perceptions concerning impaired people, most of which are negative. Over the years, opinions toward incapacity have varied significantly from one society to another. Some of these perceptions include, evil spirits possessing people with disability, them facing prejudice, and being shameful to associate with the disabled and the most common one that they are not as productive as others. A current research shows that the largest number of people, about 80 percent, perceive those with a disability as unproductive and a burden to society.
French, S. & Swain, J. 2008. Understanding Disability: A Guide for Health Professionals. Philadelphia: Churchilll Livingstone Elsevier: 4
Prior to attending this event my knowledge on the topic of disabilities was very general. I knew that people with a disability have a harder life and have to deal with people making jokes and laughing at them. I also learned that the simple things in life that people who do not have disability take for granted are some of the main things people with disabilities deal with. Things like stepping up to a curve with no curve cuts, using a public restroom, driving a car, walking, putting on clothes, or reading. My perceptive came from personal and life experiences. I have witnessed disabled people who are my friends and family, treated poorly by others.