1.1 Explain why it is important to promote awareness of sensory lost for: – individuals - It is important to promote awareness of sensory loss because we rely on our senses. We will not be able to survive without these senses. We discover the world around us by using them and we also communicate each other using our senses too. So condition of senses determinate our position in the sociality and have direct influence on our live quality, so any action taken to promote awareness how to protect senses will be benefited in the future to individuals. – service provision - it is important to promote awareness of sensory lost for service provisions such as: public transport, governance offices or surgeries, cinemas to give possibility for people with sensory lost deal with issues, problems, enquiries and other things on their own as much as they are capable to that. Make them as much independence as possible. Necessary is only appropriate equipment …show more content…
such as: stuff marked by Brail, sign language or hearing system for people with hearing aid, using large printed words rather than joined-up writing. Bigger and brighter or bigger contrast screams are more suitable for vision impairment people. – societal perceptions and attitudes – all sociality should be aware and well educated about sensory lost and how to support/help people with sensory lost.
These people must be treated with respect and equally. We should help them only when they need help, because very often they can do all for their own. Any form of discrimination due to their impairment is absolutely nonacceptable. 2.1 Outline own role in promoting awareness of sensory loss. Myself as a professional health assistant have a lot possibilities to promote awareness of sensory lost at work to my colleagues, relatives or local community. I can talk to those around me about all I know about sensory lost issues. I can raising awareness by giving just simple day life examples how to avoid risks of damage or how to protect senses, where to go if someone is concerned about his/her specific senses. 2.2 Outline the roles of others who may play a part in promoting the awareness of sensory loss Others who may play a part in promoting the awareness of sensory loss
are: Health professionals - promotion sensory healthily lifestyle, explain the anatomy and physiology of human`s senses, advise about specialist equipment and adaptions to home if is needed. Social professionals - developing and improving access to services for this group of people. Sensory Support Team - provide information on local support groups, awareness of the barriers that many sensory lost people faced. 2.3 Establish the role that individuals play in promoting awareness of sensory loss. The role that individuals play in promoting awareness of sensory loss might be so important because an individual can explain own worlds how his/her life has changed since lost sense. That promotion of awareness may be so convincing, because it would be a real story of a real person, how the life of sensory lost person look like. Descriptions how sometime these people have to struggle in their daily lives and how to adapt in the new realities.
What I found most interesting about Jarashow’s presentation were the two opposing views: Deaf culture versus medical professionals. Within the Deaf culture, they want to preserve their language and identity. The Deaf community wants to flourish and grow and do not view being deaf as a disability or being wrong. Jarashow stated that the medical field labels Deaf people as having a handicap or being disabled because they cannot hear. Those who are Deaf feel as though medical professionals are trying to eliminate them and relate it to eugenics. It is perceived that those in that field are trying to fix those who are Deaf and eliminate them by making them conform to a hearing world. Those within the Deaf community seem to be unhappy with devices such
They are human beings determined to make something good in their lives. Across the world, people with disabilities have poorer health outcomes, lower education achievements, less economic participation and higher rates of poverty than people without
There has to be an understanding of how the ear works, what hearing loss is before looking at the treatments for hearing loss. Hence the essay will go through how the ear works and what causes hearing loss first. Then it will explain the diagnosis process before focusing on the treatments. the essay will be exploring the past, current and the possible future treatments. The essay will also touch upon other ways in which hearing impaired people cope with hearing loss.
Societies could also come together so that it can enable D/deaf individuals to bond with and show hearing people how to communicate accurately and fluently. This will allow D/deaf individuals to feel like they belong in their community, which will make them feel a sense of security and also enables them to feel less isolated.
should never be defined or recognized by their disability but rather on their strengths and how far each
In fact, most of the handicapped people in society do not appreciate being treated in a way different from anyone else. They just want to be accepted as human beings.
Deaf and hearing impaired individuals are know longer an out cast group. They now have there own deaf community. Deaf individuals do not consider themselves having an impairment, handicap, or any type of disability. They believe that through the use of sign language, other communication skills, and technology that there deafness is the way they are supposed to be. Many people who have perfect hearing can not understand deaf people and why they embrace there deafness instead of trying to receive hearing and get rid of there handicap. However not all deaf people have th...
National Institute of Health. (2011). National Institute on Deafness and other communication disorders: Improving the lives of people who have communication disorders. National Institute on
Hearing people can have a place in the Deaf community. Each minority group tends to welcome genuine allies and the Deaf community is no exception. But it is important for people who hear to remember our role as allies. We join the community to show our support, not to lead. We can help educate other hearing people, but we are not missionaries to bring Deaf people into the mainstream. Deaf people are the appropriate leaders of their own civil rights movement and teachers of their children. Our role is not to give Deaf people a voice; it is to make sure that the voice already present is heard. And we can do that. We can teach other hearing people to listen.
Furthermore, Jampel (2010) explained that after disclosing her hearing impairment to her clients, she developed better relationship in the process. For her, not being able to hear allowed some clients to feel that she was a better listener and relate to her. I think I could relate to that statement because my client was able to move past the religion barriers and we were able to move towards our goals. She did acknowledged not hearing back from some of her clients after disclosing her impairment, because those clients didn’t feel like she will be able to understand them.
Provided with the viewpoints on both the medical model and social model of disability, it is clear that these two concepts differ in terms of the definition of disability as well as the attitude of society towards people with disabilities. It is evident that people with disabilities veer towards the social model rather than the medical model. It is essential to acknowledge that Deafness is categorised as a medical disability within the individual as well as a societal disability, as society is not equipped enough to deal with the communication barriers that stem from hearing impairments.
While these three authors have different reasons to write their essays, be it media unfairness, ignorance, or ethical disputes, they all share a basic principle: The disabled are not viewed by the public as “normal people,” and they are unfairly cast away from the public eye. The disabled have the same capacity to love, desire and hurt as any other human being, and deserve all of the rights and privileges that we can offer them. They should be able to enter the same buildings, have representation in the media, and certainly be allowed the right to live.
Hearing is known to be an automatic function of the body. According to the dictionary, hearing is, “the faculty or sense by which sound is perceived; the act of perceiving sound,” (“hearing…”). Hearing is a physical and involuntary act; therefore, unless one is born with a specific form of deafness, everyone has the natural ability to hear sounds. Sounds constantly surround us in our everyday environments, and because we are so accustomed to hearing certain sounds we sometimes don’t acknowledge them at all (or “listen” to them). The dictionary definition of listening is, “to give attention with the ear; attend closely for the purpose of hearing,” (“listening…”).
People with disabilities often face societal barriers and disability evokes negative perceptions and discrimination in society. As a result of the stigma associated with disability, persons with disabilities are generally excluded from education, employment, and community life, which deprives them of opportunities essential to their social development, health and well-being (Stefan). It is such barriers and discrimination that actually set people apart from society, in many cases making them a burden to the community. The ideas and concepts of equality and full participation for persons with disabilities have been developed very far on paper, but not in reality (Wallace). The government can make numerous laws against discrimination, but this does not change the way that people with disabilities are judged in society.
My instructor had informed us about people with hearing impairments and disorders, but I never thought much about it. After this assignment, I realized how hard it is to have your hearing impaired. I had the luxury of being able to take out my plugs and fix my impairment if I became to overwhelmed or stressed. Those who are impaired do not have such luxury. I did not expect as much of a psychological element to this assignment as there was. There were times where I felt anxiety stirring inside of me. I became anxious if I missed something. The first day back with un-impaired hearing was memorable. I kept thinking to myself how hard short conversations would be if I was impaired. Moving forward, I have a better grasp of what hearing impairment really is and how hard it is to live with. I will be more conscious of my hearing because I never want to experience fulltime