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S4.2 – I thought the building was c1919? I agree this needs to change to 1919 and 1940 is incorrect. S4.3 – what access controls could you use to the wheelchair access – keypad type? Generally, if it is only visitors, then a call point would be sufficient.
Karen recently bought Gary a motorized wheelchair for Gary to get around easier. 17.1 What if… Gary is having difficulty getting around the house, due to lack of mobility? You are doing an initial home health visit with him. What things do you need to watch for to advise Gary to be safe in the home and when Gary goes out?
In “Am I MS?” Miriamne Ara Krummel talks about her personal journey she endured dealing with multiple sclerosis. Krummel further explains at the end how she was finally able to accept her diagnosis and to embrace it. She finds that it’s important to be open about the disease. She believes that, “it might be helpful if more people would talk about death and dying as an intrinsic part of life” (76-77).When she was first diagnosed, she had a difficult time coping with MS.
Peter Van Daan lived in the secret annex with everybody and was a key part of the annix. Everybody living in the secret annex was captured and sent to different camps on On 4 August 1944,Peter Van Daans real name is Peter Van Pel they changed is name for the the script. Peter Van Pels was born on November 8, 1926 in Osnabrück, Germany. He died May 5th 1945 he was 18 years old when he died, he died while on the death march. He went to school at Jewish Lyceum, he had no siblings.
This article can turn out to be an inspiring article for people who are suffering from multiple sclerosis or other disabilities. Mairs begins her introduction with a hilarious event which is an attention grabbing for a reader. Then she
The disease that Dale Maxin has is known as Parkinson Disease. This disease has affected Dale 's life in a very negative way. It has caused him much grief. Medication helped him to cope with Parkinson for a period of time, however; even the medication has reached a point where it n longer helps. His wife is who he has to depend on with help for everyday things.
Kurt inspired a young man by the name of Waryk Holmes who was diagnosed with a form of cerebral palsy soon after his birth. Soon after Kurt shared his story to Waryk, he was inspired to compete in wheelchair racing in his local town. Waryk has now gone on to win the under 20’s gold in the 100 metres wheelchair race at the Athletics ACT Championships and has achieved and accomplished many of his life goals due to Kurt’s sympathy and understanding. Kurt’s overall personality displays characteristics that can change people’s lives by showing courage, support, compassion, and resilience to everyone that he meets throughout his life. Kurt Fearnley has and most likely will continue to impact communities and people throughout Australia.
Learning How to Live Do you know how it feels to live when you are unable to do things which make you happy? Diseases set a parameter to the way you live. Lou Gehrig’s disease is a neurological disorder with no cure, and death is the outcome. In the short story “Learning To Fall,” the author Philip Simmons, who is suffering with Lou Gehrig’s disease leads his life with his beliefs and strengths; he is an inspiration to those who have lost hope in their life.
Nancy Mairs forces a sharp-witted and blunt tone on the reader in her essay, “On Being A Cripple.” A new perspective is explored, on being disabled as well as the word “crippled” which is found offensive by most of society. While keeping the piece light and relatable, she shines a light on the guilty pity thrown on the disabled, treatment no one asks for. Although it is a generally light piece, Mairs uses humor, anecdotes, and diction to improve the treatment of physically disabled. Humor- Mairs lives with multiple sclerosis, and when the reader realizes this it immediately makes them feel sympathy for her.
“2.2 million people in the United States depend on a wheelchair for day-to-day tasks and mobility. 6.5 million people use a cane, a walker, or crutches to assist with their mobility”. Every single day, people varying in ages, struggle to live their lives due to conditions out of their control. Whether it be life threatening or not, it can have effects that are both socially and emotionally harming. Although some of them may change appearances on the outside, other people cannot forget that all people, not matter the disability, have brains and personalities of their own that may not be seen to the human eye.
After becoming paralyzed in a car accident, Andre Dubois remembers his viewpoint of the disabled before he became one by stating, “..and that’s how I thought of people in wheelchairs before I became one: stout-hearted-folk wheeling fast on sidewalks, climbing curbs, and of course sometimes falling backward, but that seemed to me like slipping and falling on the outfield grass while you’re chasing a fly ball,”
Tim Ferguson, Australian comedian, author, and star of the nineties comedy group the Doug Anthony All Stars, publically revealed in 2012 that he suffers from Multiple Sclerosis (MS) (Franks, 2014). He first noticed symptoms when he was around 18 years old but chose to ignore them as a temporary product of his lifestyle (Gearin, 2012). After several episodes of paralysis and numbness, also known as paresthesias (Baquis & Shenoy, 2014), on his left side (Ferguson, 2013) he was diagnosed with MS in 1995 (Franks, 2014). Mr Ferguson is one of an estimated 0.1% of the Australian population with MS and one of 46% of Autralians with MS who require some form of mobility assistance (Australian Bureau of Statistics, 2013). MS is thought to be caused
So far in my career, some of my favorite successes include: supplying assistance to families from low socioeconomic status (SES), fostering self-assurance in children with speech delays, and switching from the picture exchange communication system (PECS) to the augmentative and alternative communication (AAC) method. Through my current employer, I have the opportunity to assist low-SES families who otherwise would not have access to these services. Most recently, I participated in a state fair hearing to advocate for a patient receiving adequate frequency for speech therapy. Oftentimes, my job can be as simple as helping someone overcome the fear of being ridiculed by peers due to a speech impediment. I have used articulation therapy to eliminate sound errors before getting on stage for a school play.
People with disabilities and their caretakers are stigmatized for not being able to keep up, but they are not viewed as not having a “real” disability if they are too productive. Instead of viewing this as a symptom for their disease or disability, Hillyer believes this is a healthier way of living, and she encourages her readers to adopt similar techniques for managing their responsibilities. She especially criticizes the unrealistic, fast-paced speed that women are expected to maintain, despite personal obstacles. Hillyer, having lived in the intersection between the feminist and disability communities for most of her life, emphasizes the importance of allowing women to abandon the traditional concept of a highly productive “superwoman” and instead replace it with the knowledge that every woman dealing with a disease or disability, in themselves or loved ones, is a
In the essay, “On Being a Cripple,” Nancy Mairs uses humorous diction and a positive tone to educate people about life as a cripple and struggles of people with disabilities. She does this to show how hard it is to be disabled and how it differs from the life of someone without a disability. She talks about the struggles and the fears that disabled people must deal with on a daily basis. Mairs use of rhetoric creates a strong sense of connection and understanding for the reader. Nancy Mairs is successful in using detailed imagery, diction, and tone to educate her readers about the difficulties of living with a disability.
