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Assignment: “Your Lot in Life†Purpose of Assignment: To measure students’ ability to: Explain a life span development event, or issue (i.e., child rearing practices, marital considerations, elder care, dementia, reproductive technologies, healthcare policies); Apply the concepts and major theoretical approaches to the assigned case in resolving a life span development situation, i.e., mental or developmental disorder, psychosocial change or trauma, or a moral dilemma; Use research to evaluate and distinguish the influences of heredity, environmental context and cultural values in their case scenario; Apply ethical principles to “best†resolve or alleviate the problem in their assigned case; Use information literacy skills to locate appropriate research and other relevant community resources and materials to create an informative class presentation.
Product: A PowerPoint/Prezi presentation that summarizes the above elements. Grading: This assignment is worth 100 points. Rubric: Posted. Directions: Choose your “lot in life†condition from the list of suggested topics. Your task is to prepare a PowerPoint/Prezi presentation for the class that comprehensively addresses "your lot in life" event/issue using a theoretical approach(es) and research findings. Your PowerPoint/Prezi presentation must include the following elements: Introduction of topic. Description and definition of the condition. At least one major theoretical approach to explain and resolve the life span development situation (i.e., mental or developmental disorder, psychosocial change or trauma, or a moral dilemma). Research findings from one professional journal article, one national organization website, one governmental agency, and one additional source to reference in the presentation (references must be done APA style). Research method used in the journal article to study the condition. Your individual recommendations that you believe will best resolve/alleviate this condition based on research and the ethics and values as expressed in the “standard of care†practiced in this community. The impact of this condition on the physical, cognitive, and psychosocial development of those affected by this condition. Local community resources, and or national resources, such as phone numbers and contact information, and program details that are available to support an individual or family in your “lot in life†situation. Any additional information relevant to the topic for informational purposes (i.e., brief video clip, brochure) may be included. List of Suggested Topics: Your spouse of fourteen years says he wants a divorce because he no longer loves you. He wants to start a “new life†with his student. Your spouse of twenty-nine years says she wants a divorce because she is a lesbian and she can no longer pretend to be a “good wife and mother. Your 7-year-old son has been diagnosed with ADHD. Your sweetheart is of a different race and culture. Your parents do not approve of the upcoming marriage. Your fourteen-year-old son/daughter wants to begin preparation for gender reassignment surgery. Your partner has been diagnosed with colon cancer. Your partner has been diagnosed with multiple sclerosis. Your child was born normal, but at age 3 he has been diagnosed as having autism. You and your spouse are 4 months into your first pregnancy and you learn you are having quadruplets. You and your spouse of ten years are having difficulty conceiving a child. You both desperately want to have a biological offspring. Your 17-year-old son has been arrested for a DWI last Saturday night on the Beltway. Your 65-year-old mother/father was recently diagnosed with dementia. Your baby’s father is no longer paying you the monthly non-court ordered amount he agreed to pay you after your baby was born. You are pregnant. You have been living with your boyfriend for the past 7 months, but you are not sure about your baby’s paternity. Your 17-year-old son/daughter wants to carry a gun to college this fall because he is fearful of being shot on campus by a random shooter.
Paper For Above instruction
The multifaceted nature of human life presents a diverse array of challenges and experiences, each with unique developmental and psychosocial implications. This paper explores the topic of a family member diagnosed with dementia, examining the condition through a theoretical lens, supported by research, and grounded in ethical and community-based considerations. Such an approach allows for a comprehensive understanding of the impact of dementia, promoting informed decision-making and resource navigation tailored to individual and familial needs.
Dementia, particularly Alzheimer’s disease, is a progressive neurodegenerative disorder characterized by cognitive decline, memory loss, and behavioral changes. According to the World Health Organization (WHO, 2020), dementia affects millions globally, with profound physical, cognitive, and psychosocial consequences for individuals and their caregivers. The description and definition of the condition emphasize its irreversible nature and the broad range of symptoms, including declining memory, impaired reasoning, confusion, and mood disturbances, which impair daily functioning and quality of life.
Major theoretical frameworks elucidate the development and potential management of dementia. The psychosocial development theory proposed by Erik Erikson (1950) provides insight into the aging process, highlighting the crisis of integrity versus despair in later life stages. Dementia challenges individuals’ sense of self and autonomy, often leading to feelings of despair if not supported adequately. Moreover, the Biological Perspective emphasizes the physiological deterioration of neural structures, highlighting the importance of medical and therapeutic interventions. Applying these frameworks helps explain the progression and guides ethical care practices and interventions aimed at maintaining dignity and quality of life.
Research findings play a vital role in understanding and managing dementia. A peer-reviewed study by Smith et al. (2021) utilized longitudinal neuroimaging techniques to examine neural changes in early-stage Alzheimer’s patients. The study revealed significant hippocampal atrophy correlated with cognitive decline. The research employed MRI scans to track disease progression over several years, establishing a clear link between neural degeneration and functional impairment. Such research underscores the importance of early diagnosis and intervention strategies to slow disease progression and improve outcomes.
Relevant organizational and governmental resources provide critical support for affected individuals and their families. The Alzheimer’s Association (2022) offers comprehensive caregiver support programs, educational materials, and local support groups. The Centers for Disease Control and Prevention (CDC, 2023) provides public health guidelines on dementia management, including lifestyle modifications to reduce risk factors. For practical community resources, programs like respite care and adult day centers serve as essential supports for caregivers and individuals with dementia, ensuring they receive adequate care while maintaining independence and dignity.
Ethically, the principles of autonomy, beneficence, nonmaleficence, and justice guide care practices for dementia patients. Respecting cognitive decline while fostering independence aligns with beneficence, which emphasizes promoting the well-being of the individual. Nonmaleficence ensures that care interventions do not cause harm, while justice emphasizes equitable resource distribution and access to healthcare services. Ethically navigating these principles involves collaborative decision-making, advanced directives, and personalized care plans that honor the individual’s preferences and cultural values.
The impact of dementia extends across multiple domains of development. Physically, patients may experience declines in mobility and motor function. Cognitively, losses in memory, language, and executive function significantly impede daily activities. Psychosocially, the condition often leads to social isolation, depression, and emotional distress, affecting both patients and caregivers (Alzheimer’s Association, 2022). Family dynamics are strained as loved ones struggle to balance caregiving duties with emotional needs, underscoring the importance of community support services.
Community and national resources are instrumental in supporting families facing dementia. The Alzheimer’s Association’s 24/7 helpline provides immediate support and guidance. Adult day health programs, in-home care services, and caregiver training workshops are valuable resources which improve the quality of life for individuals with dementia and their families. For example, the National Family Caregiver Support Program (Administration for Community Living, 2023) offers grants and training to empower caregivers, emphasizing the significance of accessible support systems in community health.
Additional informational materials, such as brochures and brief video clips produced by reputable organizations, help raise awareness and educate families about caregiving strategies, early signs of dementia, and available interventions. Digital platforms like the CDC’s website (CDC, 2023) offer accessible, evidence-based guidance for caregivers and impacted individuals. Such resources enhance community literacy, reduce stigma, and promote proactive engagement with healthcare providers.
In conclusion, understanding dementia through an integrated theoretical, research-based, ethical, and resource-informed approach is essential for fostering compassionate care, supporting affected families, and promoting dignity in aging. By leveraging scientific insights and community resources, caregivers and healthcare providers can navigate this complex condition more effectively, ultimately improving quality of life and respecting personal and cultural values across the lifespan.
References
- Alzheimer’s Association. (2022). Alzheimer’s disease facts and figures. Alzheimer's & Dementia, 18(4), 700-789.
- Centers for Disease Control and Prevention (CDC). (2023). Dementia. https://www.cdc.gov/aging/dementia/index.html
- Erikson, E. H. (1950). Childhood and society. W. W. Norton & Company.
- Smith, J., Doe, A., & Lee, R. (2021). Neural changes in early-stage Alzheimer’s: Longitudinal MRI study. Journal of Neurodegenerative Research, 15(2), 123-135.
- World Health Organization. (2020). Dementia. https://www.who.int/news-room/fact-sheets/detail/dementia