Quotes From Still Alice
Still Alice, October 15,2012, #14159336 Life is a precious gift. It is not about the gifts we are given in our lives, but how we use those gifts. Do we take for granted our lives and just how precious they are or does it take a tragedy to really find out? Still Alice is a moving novel describing the inevitable downward spiral Alzheimer’s disease causes and how we must appreciate all we have because at any age, our lives could change drastically. It is unimaginable how Alzheimer’s disease changes a person’s entire life, but with the support of family, friends, and colleagues, it is possible for Alice to stay true to herself, live with the disease, and remember she is not the disease, but rather still Alice (Genova). Dr.
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There is little time for being sad right when someone is diagnosed, but after that you have to be supportive and caring. It’s not the disease caretakers live with, but the person and I feel that is very crucial to remember. As the presenter said in class, “There are rules of engagement we must recognize. They live in their own reality, have their own logic, and cannot reason, therefore we need to enter their reality” (Ms. Byergo). Accepting them for who they are and who they will become with the disease is the best thing I can think I would do. It would be an honor to work with elderly and individuals with Alzheimer’s or a form of dementia. With the typical person being older than I am now, they would have so much wisdom and things to teach me. I think telling stories and sharing memories is a great way to relive the great days before the disease really takes over. I am a great listener and love hearing stories from older, wiser people because they have more fully experienced life and shared in the beauty of it. They can relive their youth through me and I could learn how to become a fantastic adult through them. It would be a great experience. Still Alice surprised me by how well written and real life it was. I felt like I was part of the Howland family and as if I was going through everything with them. It captured my attention and stole my heart. I can’t imagine going through such an experience, but if I ever do, I will be glad I read this
There is little time for being sad right when someone is diagnosed, but after that you have to be supportive and caring. It’s not the disease caretakers live with, but the person and I feel that is very crucial to remember. As the presenter said in class, “There are rules of engagement we must recognize. They live in their own reality, have their own logic, and cannot reason, therefore we need to enter their reality” (Ms. Byergo). Accepting them for who they are and who they will become with the disease is the best thing I can think I would do. It would be an honor to work with elderly and individuals with Alzheimer’s or a form of dementia. With the typical person being older than I am now, they would have so much wisdom and things to teach me. I think telling stories and sharing memories is a great way to relive the great days before the disease really takes over. I am a great listener and love hearing stories from older, wiser people because they have more fully experienced life and shared in the beauty of it. They can relive their youth through me and I could learn how to become a fantastic adult through them. It would be a great experience. Still Alice surprised me by how well written and real life it was. I felt like I was part of the Howland family and as if I was going through everything with them. It captured my attention and stole my heart. I can’t imagine going through such an experience, but if I ever do, I will be glad I read this