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Nature as a soul
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“This is where I would be missed” There were two questions I feared asking. As I prepared for the interview I wrote them in my notebook and rehearsed them, I tried to plan out the conversation, I knew what she was going to say and I planned to simply write down her words exactly as I carefully and empathetically listened as a health humanities student. Yet, completely throwing my mental preparation out the window, I was surprised by her answers. She didn’t fear death, the hardest part wasn’t the anxiety of waiting for tests to see if treatment was working, it wasn’t acknowledging her mortality nor watching cancer taking a big part of her womanhood and overall body. She simply explained, I wouldn’t say I have fears, I’m not afraid of anything. …show more content…
Smith’s narrative embodies Eric Cassel’s interpretation of suffering, in his essay, “The Nature of Suffering and The Goals of Medicine, “This woman’s suffering was not confined to her physical symptoms, [the second] is that she suffered not only from her disease but also from its treatment, [The third] is that one could not anticipate what she would describe as a source of suffering” (Cassel, 8). During our conversation I did my best to let her lead and restricted my input to the minimum. She did speak of her treatment when I asked about it but in the sense of her overall story, it was surprising to find that most of her suffering due to her illness occurred outside of hospital walls. The pain and constant nausea were hard to tolerate but it was the consequence of these symptoms that affected her the most, it was the context of the illness that caused her the suffering she believed important to speak during our limited time. When looking at Mrs. Smith further than her physical body and rather as a whole person, the extra time it took her to get ready that caused her to be late to work in the mornings and those two SQF audit points is what really hurt her spirit. Likewise, the lymphedema itself caused her pain and discomfort, but the real suffering came from it permanently slowing her pace leaving her feeling like she couldn’t efficiently do what she considered was her great contribution to her
Hutchinson, Tom “Illness and the hero’s journey: still ourselves and more”, CMAJ. 162.11 (2000):p.1597 web (date accessed).
Being diagnosed with a chronic illness is a life-altering event. During this time, life is not only difficult for the patient, but also for their loved ones. Families must learn to cope together and to work out the best options for the patient and the rest of the family. Although it may not be fair at times, things may need to be centered on or around the patient no matter what the circumstance. (Abbott, 2003) Sacrifices may have to be made during difficult times. Many factors are involved when dealing with chronic illnesses. Coping with chronic illnesses alter many different emotions for the patients and the loved ones. Many changes occur that are very different and difficult to get used to. (Abbott, 2003) It is not easy for someone to sympathize with you when they haven’t been in the situation themselves. No matter how many books they read or people they talk to, they cannot come close to understanding.
Now that the summary is out there for all who did not get to read the story let’s make some connections to everyday life. In the story is it said by the author that, “All the while I hated myself for having wept before the needle went in, convinced that the nurse and my mother we...
What symptoms classify a person to be diagnosed as sick? A cough, a sore throat, or maybe a fever. Often times when individuals refer to the word ‘sick’, they neglect to mention a common disorder, one which takes a tremendous amount of personal determination, courage and strength in order to overcome. Mental illness took the author, Joanne Greenberg, down a path complete with obstacles, forcing her to battle against schizophrenia, a chronic brain disorder resulting in delusions, hallucinations, trouble with thinking and concentration as well as a lack of motivation. This complex piece of literature was originally composed to fight against the prejudice accusations associated with mental illness, while providing the semi-autobiographical novelist
When it comes to a bad diagnosis it is often difficult for doctors to tell their patients this devastating news. The doctor will likely hold back from telling the patient the whole truth about their health because they believe the patient will become depressed. However, Schwartz argues that telling the patient the whole truth about their illness will cause depression and anxiety, but rather telling the patient the whole truth will empower and motivate the patient to make the most of their days. Many doctors will often also prescribe or offer treatment that will likely not help their health, but the doctors do so to make patients feel as though their may be a solution to the problem as they are unaware to the limited number of days they may have left. In comparison, people who are aware there is no cure to their diagnosis and many choose to live their last days not in the hospital or pain free from medications without a treatment holding them back. They can choose to live their last days with their family and will have more time and awareness to handle a will. Schwartz argues the importance of telling patients the truth about their diagnosis and communicating the person’s likely amount of time left as it will affect how the patient chooses to live their limited
Shock, anger, numbness, denial, acceptance, and fighting for one’s life, are the general phases of grief through one’s experience with cancer (cancersurvivors.org). Although discovering about one’s cancer can be excruciating, an additional agonizing reaction to a sick person is how the others are affected and their one-on-one reaction to the person. Feeling overly pitiful to one’s illness can impair the situation for the one who is ill by emotionally making the tragedy feel additionally worse. Although the extra sympathy, empathy, and compassion Hazel Grace Lancaster is treated with in The Fault In Ours Stars are intended to comfort, these exaggerated emotions have the opposite effect, further isolating and reminding her of her limited existence, but concurrently, the reality of condolences is pivotal to Hazel’s life.
3. The relation between the chronically ill patient and the body is of intertwined subjectivity, of one human dignity and human strength. This is made manifest through the patient’s continued struggle for life despite awareness of dwindling quality of health and diminishing quality of life.
After reading the title of the poem Sick Room, Langston Hughes, the reader immediately undergoes a feeling of suspense and seriousness. The title explains the room in which the woman is lying in and what her condition is. The reader can speculate that she is not in a room to bring her happiness or good news, but rather a dreary and disheartening environment. Perhaps, because it is being called a “Sick Room” it could be taking place in a hospital room. In this poem, Hughes describes the feeling of the woman who does not have much time to live. She is stuck knocking on death’s door and fighting for a little longer. However, either way she will feel pain which is forcing her to make the best out of either outcome.
Though there are several patients featured, the story centers around Cody Curtis, a woman who was diagnosed with liver cancer. At 56, she is a beautiful woman who doesn’t appear to be sick. She seems healthy and happy. However she is in constant pain and is suffering greatly. She is given a diagnosis of only six months left to live and sets a date to choose to die. She has complete control over when she will die. She can make peace with those around her and complete her life before she dies. She says that death with dignity won’t be easy, but it would be easier than the alternatives. However, she outlives her diagnosis and her quality of life continues to improve. When things take a turn for the worst, she decides to end her
In “ Sounding Board Death and Dignity, A Case of Individualized Decision Making” by Timothy E. Quill talks about a patient of his named Diane. An ordinary person but has struggled with alcoholism and depression. Quill then, with vigorous testes, finds out she has acute leukemia. Now knowing this, Quill and other doctors advised Diane about undergoing treatment as soon as possible. But she refused and just wanted to go home and be with her family. Though at this time she was not experiencing any suffering as ...
Diane was a patient of Dr. Timothy Quill, who was diagnosed with acute myelomonocytic leukemia. Diane overcame alcoholism and had vaginal cancer in her youth. She had been under his care for a period of 8 years, during which an intimate doctor-patient bond had been established. It was Dr. Quill’s observation that “she was an incredibly clear, at times brutally honest, thinker and communicator.” This observation became especially cogent after Diane heard of her diagnosis. Dr. Quill informed her of the diagnosis, and of the possible treatments. This series of treatments entailed multiple chemotherapy sessions, followed by a bone marrow transplant, accompanied by an array of ancillary treatments. At the end of this series of treatments, the survival rate was 25%, and it was further complicated in Diane’s case by the absence of a closely matched bone-marrow donor. Diane chose not to receive treatment, desiring to spend whatever time she had left outside of the hospital. Dr. Quill met with her several times to ensure that she didn’t change her mind, and he had Diane meet with a psychologist with whom she had met before. Then Diane complicated the case by informing Dr. Quill that she be able to control the time of her death, avoiding the loss of dignity and discomfort which would precede her death. Dr. Quinn informed her of the Hemlock Society, and shortly afterwards, Diane called Dr. Quinn with a request for barbiturates, complaining of insomnia. Dr. Quinn gave her the prescription and informed her how to use them to sleep, and the amount necessary to commit suicide. Diane called all of her friends to say goodbye, including Dr. Quinn, and took her life two days after they met.
Steindorf, O’Daniell, and Joy T. didn’t realize their psychological distress was related to their cancer experience — they had survived, after a...
Through the difficult, cancer-controlled lives of Augustus, Hazel, and even Peter Van Houten, we see just how bad some people have it. They must deal with the fact that what they were given is not ideal, but must be dealt with. Augustus had to deal with this up until the last days of his life, where he began to focus on his legacy and making sure his life had a purpose, which makes it evident that others will also search for things like these throughout the course of their
The following interview was held on the 1st of March 2014 over the phone. I asked my aunt a few questions and gave her the reason...
Within this memoir, Lucy Grealy is faced with distinguishing between the mental and physical pain that she is dealing with during her life. The mental pain that seems to immerse her includes the shame and guilt she feels when showing her negative reactions to the painful chemotherapy. Lucy uses the physical pain of enduring over thirty surgeries to deflect from emotional insecurity of her facial deformities. To find her inner values of her self, she must first emotionally overcome her outward