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Essays on childhood cancer
Essays on childhood cancer
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I am in the waiting room of the pediatric oncologist’s office holding my son, Michael, in my arms. As my 16 month old son naps in my arms I am reminded of the reason we’re here. I tap my foot impatiently as we wait for the test results that will impact the rest of our lives.
I remember when our world came crashing down around us, it was the same time we should be celebrating milestones. When Michael was 9 months old he was diagnosed with Atypical Teratoid/ Rhabdoid Tumor, also known as, ATRT, or even more popular, brain cancer. I am sitting in the office today waiting to find out the fate of my 16 month old angel.
The bleach white walls, the smell of sanitizer and the mellow music that fills the room make me nauseous. The nurses laughing and carrying on as though their worlds are perfect, don’t seem to notice that I am sitting here holding a child that is fighting for his life. The least they could do is shut their traps while he rests his body for the first time all day. I continue to coddle my baby boy and watch his every breath; I cannot help but notice the little miracles he gives us on a regular basis. This time we have together may look depressing to an outsider because he is sick, but to me it is also comforting because it formed a bond between us no one can take away.
“Linda?” The stout dark haired nurse named Jewel called for me from the door way leading to the patient exam rooms. I stood with Michael in my arms and our diaper bag over my shoulder. “Dr is ready to see Michael now.” She completed, with a look of sorrow written on her face. My heart sank at that moment. She may not realize it, but her face told me the results of his recent scans were not good.
Jewel led me thru the narrow halls past the e...
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...said gently releasing the rail on the hospital crib bed. I relaxed myself in the room’s only recliner ready to hold my son until he went to his forever home. The nurse maneuvered the IV pole and other machinery closer to the chair where I was sitting before finally placing my small Michael in my arms.
“Thank you.” I whispered.
Nate looked on in a daze as if he did not understand what was happening. He continued to look on without saying a word and the occasional tear.
“Hush little baby don’t say a word…” I began to sing. Michael opened one eye to peek out at me and gave a half smile, which was all he could muster.
Suddenly the breathing and heart monitor alarms started to sound. My angel had taken his final breath while in my arms. The nurse rushed in to check the equipment but quickly realized it was not malfunctioning monitors. Michael had gone home to heaven.
Mary Hoge had gone into labor Sunday 23rd of July 1972 giving birth to her fifth child, Robert Hoge. When Robert Hoge was born, his own mother didn’t want him. Robert’s mother Mary thought he was too ugly, that he was, in appearance, a monstrous baby. Robert was born with a tumor the size of a tennis ball right in the middle of his face and with short twisted legs. Robert was born in Australia, where he would have to undergo numerous operations that carried very high risk in order to try and live a “normal” life.
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...
Pediatric oncology has been so very rewarding in many ways, but also so very cruel in a few ways. The good days are great, but the sad days are heartbreaking. But beyond the death and the suffering, there is a whole other layer of
He was an outpatient, who arrived at 8 am to get ready for his surgery. Feeling I was ecstatic and enthusiastic to get back into the field of work to do my clinical rotations. Although I was ready to have a new experience at the recovery unit, I was also extremely scared, because this unit was a specialized unit, where the patient needs vital care while recovering from anesthesia.
...he will not let her die in their parents arms in the coming hours. He is dedicated to this diagnosis and goes in one last time, this time with a spoon.
Death ultimately brings individuals together and the Bundren family is no exception. Each member of this chaotic family dealt with their mother Addie’s death quite differently. Throughout the novel, Cash is the silent, hard-working type who says next to nothing about his family’s crazy nature and how he exactly feels about their current situations. I believe that Cash making his mother’s coffin outside the window was not cruel or disrespectful; it shows his loyalty and commitment to his mother. Of all the Bundren children, Cash dealt with his mother’s death through physical emotion. He worked diligently on constructing the coffin and making sure it would not slant or move during the journey to Jefferson, however, readers know that everything did not go as planned. Darl, the most rational of the group, “goes off the deep end”, so to speak because of his mother’s death. While Darl and Jewel are away getting Tull’s horses, Addie dies and Darl can see what is going on back at home. His omniscent nature makes him a wonderful narrator becau...
... joy Mrs. L got from seeing her cat. Health in this scenario is shown mostly notably when Mrs. L got relief from Morphine and stated she knew she was going to die but felt “ok for now”. Health in this case was measured by an improvement in pain and not an absence of illness. Finally, nursing in this scenario is exemplified in many ways. In the paragraph above I begin by ensuring the patient’s confidentiality. Mrs. L was placed at the center of care. I collaborated with other nurses and all those in the environment to assure the best care possible. Through direct care, teaching and advocacy I delivered the exact type of care I would wish for myself, or someone I loved, if I were in Mrs. L’s place.
One fateful day at the end of June in 1998 when I was spending some time at home; my mother came to me with the bad news: my parent's best friend, Tommy, had been diagnosed with brain cancer. He had been sick for some time and we all had anxiously been awaiting a prognosis. But none of us were ready for the bumpy roads that lay ahead: testing, surgery, chemotherapy, nausea, headaches, and fatigue. Even loud music would induce vomiting. He just felt all around lousy.
"Selena Gibson" the nurse called out after opening the closed door. I stood up and quickly moved forward toward the nurse. Stepping through the door I was ask to turn to the right and go down the hallway. Walking down the long stretch dragging my feet along the way I was scared to find out what the doctor was going to say. Turning to the left the room looked impersonal and cold. I was asked to seat in the chair and wait till the doctor came in with the results.
Cancer is a word which evokes many different images and emotions. Nothing in this world can prepare a person for the utter devastation of finding out someone has been diagnosed with cancer, especially when this person is a child. Over the past twenty five years the amount of research and the survival rate for children suffering with cancer have increased dramatically. Despite these successes, the funding for new research necessary to keep these children alive and healthy is miniscule and too dependent on short term grants. Of the billions of dollars spent each year on cancer treatments and research less than a third is contributed to researching pediatric cancer. Given the media focus on adult cancers, research for pediatric cancer is underfunded. In order to maintain the increasing survival rate of the children undergoing pediatric cancer and support those who have survived the disease, better funding is quintessential to develop and further promote research.
When one hears the word “cancer”, thoughts about how their previous life is about to change cloud the mind, but when one hears the word cancer for their child, it is a whole different outlook; the affects of childhood cancer are not only taken on by the patients, but also by their families; the affects can range from emotionally to physically, socially to financially, and even educationally. “Childhood cancer is considered rare, especially compared with adults. Still it’s the leading cause of death in children pre-adolescent, school-aged children” (Report: Childhood Cancer Rates Continue to Rise, but Treatment Helps Drive Down Deaths). Around 12,000 children in the United States are diagnosed with cancer every year and around one in five children that are diagnosed with cancer will die.
In daily practice of the pediatric oncology nurse, they find themselves experiencing predicaments as they attempt to balance providing care, communicating with and educating family, working collaboratively with medical teams, as well as advocating for the voices of their patients. An essential role in nursing is caring, compassion and empathy. ( (friberg) 50. “Caring presence is mutual trust and sharing, transcending connectedness, and experience. This special way of being a caring presence involves devotion to a client’s well-being while bringing scientific knowledge and expertise to the relationship” (Covington (2005) states, p. 169). However, part of nursing is the relief of suffering, but complex interventions often cause
...nts. We can alleviate fears and anxieties by connecting with our patients and families. In the OR, this means a warm blanket, a hand to hold, a tissue to wipe away tears, encouraging words, understanding eyes, a shoulder to lean on, and a nurse to trust." said Kelly Walsh, BSN, RN, thoracic surgery coordinator at the Hospital of the University of Pennsylvania in Philadelphia. (Unknown author, “What I Love About Nursing”). Nursing is a job for life, It just never stops giving. Everyday, there is new thing to learn, and its always the technology changing for the nurses. It gives us hope for those who shake our hands and tell us “thanks” that makes us love what we do. It’s the simplest things that are the best. But there’s nothing better than saving a another person’s live. And at the end of the day, its great to know that you gave someone else the gift of a lifetime.
We arrived at the emergency room only to find several people already there. Joey was begging me to do something to stop the pain in his back; we waited and waited and waited. Finally, in total anger and despair I set out to find someone to help. The doctor came over, examined him and asked me several questions; it was slowly becoming apparent to me that this doctor did not have any answers. Meanwhile I was growing more concerned about the unknown; what was wrong with my child? The doctor, obviously puzzled by the situation, decided to run a CBC (complete blood count). This took what felt like an eternity, suddenly the doctor became somewhat evasive, almost secretive. I was exasperated, determined to find out what was wrong with Joey’s lab report. I inched my way over behind the curtain, so I could overhear bits and pieces of the doctor’s conversation. They were discussing things like a low hemoglobin count and a high white blood cell count, then I heard it, the most devastating word I have ever heard a doctor say-Leukemia.
The first wave of bad news came in January of 2014. We were called into our typical Friday meeting however this was not a typical meeting. He began by telling us that he was diagnosed with Stage IV Lung Cancer (adenocarcinoma). Being stage four, this means the cancer has spread to other parts of his body. His face flush, eyes filled with tears he said,