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Diabetes case study in children
Diabetes case study in children
Essay on type 1 diabetes in youths
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Summary of the Article
The study entitled, “What Is It Like to Be a Child with Type 1 Diabetes Mellitus?” by Sparapani, Jacob, and Nascimento (2015) is essentially where nineteen children between the ages of seven and twelve years old, who were diagnosed with type 1 diabetes and had the diagnosis for at least one year were chosen and had parental consent to participate in the study while they were being treated in an outpatient clinic of a university hospital in Sao Paulo, Brazil. The researchers (Sparapani, Jacob, and Nascimento, 2015) had the children make puppets that represented not only themselves but also people that they interacted with on a daily basis such as family members, friends, teachers, as well as devices such as syringes and glucose monitors. In order to collect data, the researchers used puppets and a stage in order to “create scenes that the children would encounter in their daily lives in order
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to get the children to talk about their daily routine and how they would manage their diabetes throughout the day” (Sparapani, Jacob and Nascimento, 2015, p. 18). Through their collection of data, Sparapani, Jacob and Nascimento (2015) analyzed the data and were able to pin point the “four types of feelings that emerged that described the experience of ‘what it is like’ to be a child with type 1 diabetes mellitus; which were conflicting desires, insecurity, fear and pain” (p.19). Analysis and Critique “Type 1 diabetes mellitus is a common chronic disease that effects a person’s quality of life, psychological well-being and sense of control, and approximately two-thirds of all diabetes cases are diagnosed in children” (Sparapani, Jacob and Nascimento, 2015, p.17). The purpose of this study was to increase understanding of what it is like for a child to have type 1 diabetes and to target what factors may hinder disease management (Sparapani, Jacob and Nascimento, 2015, p.17). The article entitled, “What Is It Like to Be a Child with Type 1 Diabetes Mellitus?” not only was successful in increasing ones understanding of this chronic disease from a child’s standpoint; it also was very enlightening about how a nurse could better care for the entire patient by teaching their patients about what is going on in their body, and to realize that it effects the whole person and their quality of life. Dealing with type 1 diabetes mellitus is a disease that effects ones “quality of life, psychological well-being, and sense of control” (Sparapani, Jacob and Nascimento, 2015, p.17) Problems and Purpose The article provides information that Sparapani, Jacob and Nascimento gathered through interviewing 19 children through the use of puppets. Sparapani, Jacob and Nascimento decided to perform this study because they had found that there was very little research done on examining ‘what it is like’ to be a child with type 1 diabetes and thought that by “investigating children’s own experiences with living with diabetes, nurses may promote successful disease management and build educational and psychosocial programs that best support the needs of children with type 1 diabetes and their families (Sparapani, Jacob and Nascimento, 2015, p. 17). There did not seem to be many problems with this study in general the only thing that could have possibly made it better would be to have included the questions that were asked of the children and having a larger sample group of children for the study that were from various regions rather than just one outpatient clinic of a university hospital in Brazil. Research Method Sparapani, Jacob, and Nascimento (2015) chose to perform qualitative interviews with 19 children about their daily life and what it is like to have diabetes. The sample of children “consisted of 13 girls and 6 boys, all between the ages of 7 and 12 years old, and all having been diagnosed with type 1 diabetes for at least 1 year, but not more than 10 years” (p.19). From the qualitative interviews that were performed with puppets to get the children to open up about their daily lives and what it is like to live with diabetes as a child Sparapani, Jacob and Nascimento found out that there were major themes that arose after talking to the children, those being: “conflicting desires; insecurity, fear and pain; worry about long term effects; inadequate knowledge of the disease; prejudice, rejection and shame” (2015, p.19-20). Relationship between Study’s Problem and Method Sparapani, Jacob and Nascimento (2015) assert that with finding out the child’s perspective of what it is like living with diabetes, that nurses could play a more active role is successful disease management and build more educational programs to help support not only the children with type 1 diabetes, but also their families (p.17). The choice of using puppets to perform qualitative studies with these children was extremely appropriate considering the age range that was used by Sparapani, Jacob and Nascimento (2015) and probably the most effective way to get the children to open up about their daily lives and what it is like to live with diabetes as a child. Evaluation and Recommendations Sparapani, Jacob, and Nascimento (2015) were very thorough with their study using puppets to perform qualitative interviews with children between the ages of seven and twelve years, who were diagnosed and had type 1 diabetes mellitus for at least 1 year in order to examine their “thoughts, feelings, and how they managed having diabetes.” They did not provide the specific questions that they had asked the children; however they did include transcribed answers that were made by the children that also included the participants’ nonverbal behaviors.
Upon the analysis of the answers given by the children, Sparapani, Jacob and Nascimento (2015) determined that there were “four types of feelings emerged that described what types of experiences of ‘what it is like’ to be a child with type 1 diabetes: conflicting desires, insecurity, fear and pain.” Yet it was unclear as to how they made this determination besides them stating that after going through all the passages, categories and subcategories occurred, which in turn allowed data coding to be
accomplished. Although this study did provide a lot of qualitative data, it really should have had more participants than just 19 children, just to have a larger sample to make it easier to find any outliers. To make the study even better, it should have included children from more than just one university hospital, just to ensure the results of Sparapani, Jacob and Nascimento (2015) did not only reflect the thoughts and feelings of what it is like to be a child with type 1 diabetes in just that region. New Information Learned The new information learned from this study was that when caring for a patient, especially a child, there are many things to take into consideration besides just treating the disease. Factors such as letting them know what it is going to feel like, as far as pain, making sure that they understand what is going on with their body, explaining to the child that there is nothing that they need to be ashamed of, and attempting to be there for them if they do have any questions about how to deal with everyday lifestyle changes that are required due to the diagnosis of type 1 diabetes. How the information of the article will be helpful to the students in the clinical area during this semester The information of this article will be helpful to the students in the clinical area during this semester because it provides a child’s insight on how it is to have and attempt to manage having Type 1 diabetes mellitus. It also provides ideas for nurses, as to effective ways to develop educational activities for children who are diagnosed with type 1 diabetes as well as reminders of things to think about when interacting or treating a young child who has diabetes; such as the pain of the needles, the fear of the needles, and the other emotional and psychosocial aspects that come along with having any long term disease. Reference Sparapani, V.C., Jacob, E., & Nascimento, L. C. (2015). What Is It Like to Be a Child with Type 1 Diabetes Mellitus?. Pediatric Nursing, 41(1), 17-22.
My patient Hannah is a 10 year old 4th grade student who loves volleyball and was just diagnosed with type 1 diabetes mellitus. I’m going to explain to you what her disorder is, the signs and symptoms, causes of this disorder, body changes, economic impact, and how she will manage this disorder especially at such a young age.
The case study chosen for this assignment is case study #2: Hannah is a 10-year-old girl who has recently been diagnosed with Type 1 Diabetes Mellitus. She is a 4th grade student at Hendricks Elementary School. Prior to her diagnosis, Hannah was very involved in sports and played on the girls’ volleyball team. Her mother is concerned about how the diagnosis will affect Hannah.
Case study: Carol is 17 years old and was diagnosed with Type 1 diabetes at the age of 7 years. Carol has had a recent hospital admission for dehydration and high blood glucose. During the admission Carol was found to be 6 weeks pregnant. Prior to the admission she had been experiencing weight loss and changes in mood.
When looking at the common signs and symptoms of the disease, we understand that the symptoms are more readily recognizable in children than in adults. In Type I, we typically see a variety of symptoms shown by the child. Common symptoms within the Type I disease are typically related to the child’s low blood sugar. When this happens the child experiences, in most case, abdominal pain**, weight loss, thirst**, nausea, blurry eyes**, sweaty**, dry skin, and fatigue**. (Wong, Hockenberry, Wilson, 2015)
Seiffge-Krenke, Inge. Diabetic Adolescents and Their Families: Stress, Coping, and Adaptation. Cambridge, New York: Cambridge University Press, 2001.
Specific purpose: To inform my audience about what diabetes is, what causes this condition and its health effects.
Diabetes is one of the leading chronic causes of deaths in children and adolescent’s in the United States. Diabetes mellitus is a group of diseases that is characterized by high levels of glucose in the bloodstream resulting from defects in insulin production, insulin action or even both (Overview, 1). Diabetes is a serious health issue and can be associated with premature death or serious complications. Timely diagnosed treatment of diabetes can delay or prevent any onset of long-term complications, such as damage to blood vessels, kidneys, gums, skin, teeth, and many other complications (Overview, 1). Diabetes can be difficult to deal with during the time of adolescence. People with diabetes or those who have family members with diabetes should be very well informed (Cho, 1).
The program is based on participatory education where the facilitator creates an environment that allows discovery where group participation and involvement is essential. This type of education enhances knowledge and skills for self-management, develops a critical understanding of the disease, promotes solidarity and community involvement and helps to achieve self-efficacy and change behaviors for better diabetes control ("Everyone with Diabetes",
My interest in this topic is a result of recent experiences with Diabetes Mellitus, Type 1 (DMI), especially with the following two instances: a young adult patient admitted at the hospital following a DKA episode during one of my nursing rotations and one of my instructors with type 1 diabetes. Also, my father was diagnosed with type 2 diabetes, this has increased my eagerness to study and explore more about the disease.
This cause me to ask questions, “Why me?” Why is this disease a real thing. Why am I different? As I grew older, I started to see how I was different than most children my age. I was diabetic, but that was not all, I was more of an adult than other children. I had so many responsibilities to deal with because of being diabetic. As I felt I had grew up fast, meant I thought I didn't need help because I could do anything, yet you need help to grow. As it became summer, it had been a year of having diabetes. I went to camp. Camp Joslin which is a summer camp for children with diabetes. Honestly is was very bizarre to think that everyone there had something in common. I had never been around so many diabetics in my life. We all had to test their blood sugar and take insulin. For the week I was there, everyone was the same. It gave me a sense of being like everyone else. I got a chance that none of my friends got, to go to camp Joslin. I was thankful and happy. As I continued to grow older and went to high school, I was still different. I began to realize that being different wasn’t really a curse, but it was a gift. I came to the conclusion that even when life is hard, you can always handle it. The question “Why me?”, does not solve your
Creating solutions such as enhanced workshops to educate the children and caregivers can reduce the amount of stress for the family by creating detailed plans of care. Developing programs to monetarily assist those that cannot afford the extra costs associated with the disease reduces the financial stress. Programs to ensure that more children can assist the camps offered to build the self-esteem of these children . Education to eliminate the misconception that Type 1 Diabetes is a disability but instead a self-limiting disease when there are no available resources; good management of this disease will be excellent choice in preventing complications but being knowledgeable will help in making better choices for a healthier lifestyle and in turn a longer life.
Type 1 diabetes, is an incurable but treatable disease which can occur at any age but is mostly found in children due to the high levels of glucose in the blood (Eckman 2011). Juvenile diabetes affects about 1 in every 400-600 children and more than 13,000 are diagnosed yearly (Couch 2008). Type 1 Diabetes means your blood glucose, or blood sugar, is too high. With Type 1 diabetes, your pancreas does not make insulin. Insulin is a hormone, which helps glucose gets into your cells to provide energy. Without insulin, too much glucose stays in your blood. Over time, high blood glucose can lead to serious problems with your heart, eyes, kidneys, nerves, gums and teeth (American Diabetes Association). Previous research has suggested proper insulin management, a balanced diet and exercise will help maintain glycemic control and lessen the chance of complications (Couch 2008).
When living with a long-term health condition it can for some people present them with many new challenges. Not only does it take time for them to adapt and accept their illness but also they may feel affected not just physically, but psychologically, culturally, and sometimes even personally such as financial or relationships with family and friends. In this essay, I will examine in turn the main challenges people with diabetes face.
Some people thought that having a disease could ruin their life, but some people, learn to overcome it. I was diagnosed with type one diabetes when I was four years old and have been living a semi-normal life ever since, with complications of course. Someone once said that you cannot overcome an obstacle unless you learn how. I am one of those people that learned. That learned to overcome my obstacle.
Point blank, diabetes is a serious disease and causes major effects on people’s daily lives. In a society where food comes in such abundance, people are overeating. Compared to the beginning of the twenty first century when only about five percent of the population had diabetes (Nazarko, 2009), today that number is rising and continuing to do so. This is starting to affect the health of children by being diagnosed with diabetes at a young age. When a child has diabetes it becomes very serious since children are at such a young age to deal...