This document appears to be a capstone presentation for a psychology student interning at Caris Healthcare, a hospice care organization. The presentation covers research related to caring for patients at the end of life, including topics like cultural awareness, religion, caregiver burden, and the "sandwich generation". It also provides demographics of the student's patients and outlines learning objectives achieved through the internship. The presentation demonstrates how research can inform providing culturally sensitive end-of-life care.
This document provides information about hospice care services from the Midwest Palliative & Hospice CareCenter. It discusses what hospice is, the goals of comfort and quality of life for patients, where patients can receive care, eligibility which includes a prognosis of 6 months or less, the hospice care team, common questions about services, how to discuss hospice with a loved one, bereavement support services, and resources for additional information.
Hospice aims to treat the whole person rather than the disease and focus on quality of life over length of life. It provides comfort and dignity for patients dealing with terminal illness through physical, spiritual, and emotional support for patients and their families. There are several ethical issues around patient autonomy, access to care, and overcoming barriers for underserved groups. A lack of communication and cultural understanding can negatively impact minority groups' access and experience with hospice care. Additionally, over-reliance on technology risks losing personal interactions that are important for end-of-life care.
This slideshow is a tour of Cancer Awakens - www.cancerawakens.com - showcasing how our site, newsletter and social media channels support the cancer community.
Ethics at the End of Life and Introduction to Hospice and Palliative Care for Medical Students. Exploration of feeding tubes, code status, when to stop chemo. Discusses cases and the ethical principles and values that are the basis for disagreement in care and what to do when there is a conflict in ethical principles themselves. Also provides an introduction to decisions of last resort including physician aid in dying, palliative sedation and voluntary refusal of nutrition and hydration.
Hospice Care - Is It Right for You or Your Loved One?Theresa Lynn
This presentation from Wings of Hope Hospice in Allegan, Michigan describes the benefits of hospice care, when hospice care might be appropriate and the geographic area Wings of Hope serves.
1. Cancer and its treatments can impact patient sexuality through biological, physical, and psychosocial factors like changes to the body, fertility issues, and emotional distress.
2. Nurses should conduct comprehensive assessments of patient sexuality through open communication, addressing cultural and personal factors, and utilizing models like PLISSIT.
3. Nurses can manage side effects on sexuality through treating symptoms, educating on intimacy options, and referring patients to supportive resources for physical and emotional wellbeing.
4. Nurses must overcome barriers like embarrassment through active listening, normalizing issues as treatable side effects, and focusing on holistic care of the patient's wellness.
Psychosocial aspects of cancer care by phillip odiyoKesho Conference
This document discusses the psychosocial aspects of cancer care and challenges with patient communication and survivorship. It outlines the complexity of psychosocial issues associated with cancer and how the doctor-patient relationship has evolved from a paternalistic model to one that emphasizes patient autonomy. Effective doctor-patient communication is important for clinical reasoning, patient satisfaction, and medication adherence. However, studies show that doctors often miss patients' main concerns and psychosocial problems. The document advocates for a patient-centered approach and communication styles like SPIKES and BATHE that focus on the patient's perspective and psychosocial context across the cancer care continuum.
This document provides information about hospice care services from the Midwest Palliative & Hospice CareCenter. It discusses what hospice is, the goals of comfort and quality of life for patients, where patients can receive care, eligibility which includes a prognosis of 6 months or less, the hospice care team, common questions about services, how to discuss hospice with a loved one, bereavement support services, and resources for additional information.
Hospice aims to treat the whole person rather than the disease and focus on quality of life over length of life. It provides comfort and dignity for patients dealing with terminal illness through physical, spiritual, and emotional support for patients and their families. There are several ethical issues around patient autonomy, access to care, and overcoming barriers for underserved groups. A lack of communication and cultural understanding can negatively impact minority groups' access and experience with hospice care. Additionally, over-reliance on technology risks losing personal interactions that are important for end-of-life care.
This slideshow is a tour of Cancer Awakens - www.cancerawakens.com - showcasing how our site, newsletter and social media channels support the cancer community.
Ethics at the End of Life and Introduction to Hospice and Palliative Care for Medical Students. Exploration of feeding tubes, code status, when to stop chemo. Discusses cases and the ethical principles and values that are the basis for disagreement in care and what to do when there is a conflict in ethical principles themselves. Also provides an introduction to decisions of last resort including physician aid in dying, palliative sedation and voluntary refusal of nutrition and hydration.
Hospice Care - Is It Right for You or Your Loved One?Theresa Lynn
This presentation from Wings of Hope Hospice in Allegan, Michigan describes the benefits of hospice care, when hospice care might be appropriate and the geographic area Wings of Hope serves.
1. Cancer and its treatments can impact patient sexuality through biological, physical, and psychosocial factors like changes to the body, fertility issues, and emotional distress.
2. Nurses should conduct comprehensive assessments of patient sexuality through open communication, addressing cultural and personal factors, and utilizing models like PLISSIT.
3. Nurses can manage side effects on sexuality through treating symptoms, educating on intimacy options, and referring patients to supportive resources for physical and emotional wellbeing.
4. Nurses must overcome barriers like embarrassment through active listening, normalizing issues as treatable side effects, and focusing on holistic care of the patient's wellness.
Psychosocial aspects of cancer care by phillip odiyoKesho Conference
This document discusses the psychosocial aspects of cancer care and challenges with patient communication and survivorship. It outlines the complexity of psychosocial issues associated with cancer and how the doctor-patient relationship has evolved from a paternalistic model to one that emphasizes patient autonomy. Effective doctor-patient communication is important for clinical reasoning, patient satisfaction, and medication adherence. However, studies show that doctors often miss patients' main concerns and psychosocial problems. The document advocates for a patient-centered approach and communication styles like SPIKES and BATHE that focus on the patient's perspective and psychosocial context across the cancer care continuum.
Palliative Care What Is Palliative MedicineIndranil Khan
This document provides information about palliative care from Dr. Indranil Khan, a palliative care provider in Kolkata, India. It defines palliative care as a holistic approach to improving quality of life for patients with chronic or life-threatening illnesses and their families through management of physical, psychological, social and spiritual problems. It outlines who can benefit from palliative care, the dimensions of care provided, components of care like home visits and access to pain medications, the multidisciplinary palliative care team, and common myths about palliative care.
Ethics presentation given at Providence Health Care on 2/19/16 as a part of a day-long nursing oncology conference. Discusses the fundamental clinical ethics consultation approach and discusses in narrative the relevant ethics cases that are common to oncology practice
Presented at Kansas City University of Osteopathic Medicine 10/27/15 in Lecture Series in Bioethics. See live presentation here: https://www.youtube.com/watch?v=Dr3g3PeVKeo
This document discusses hospice and palliative care. It begins by stating some key facts about death and the needs of dying patients. It then discusses why palliative care is needed to relieve suffering at the end of life. Palliative care aims to provide physical, psychological, social and spiritual support for patients and their families. The document outlines some obstacles to palliative care, such as delays in decision making and lack of resources and facilities. It compares the hospice approach, which specializes in end-of-life care, to the palliative care approach. The document argues that hospice may be better suited than palliation for Iraq due to its focus on minimizing costs, accommodating cultural needs, and being cost
Ethical, moral and legal issues in oncologyManali Solanki
The document discusses end of life care and ethics in oncology nursing. It defines end of life care as treating, comforting, and supporting those living with or dying from chronic life-threatening illnesses. It also discusses the importance of communication, education, and addressing spiritual-psychosocial needs of dying patients and their families. The document outlines several ethical issues that may arise in end of life care, such as medical futility, terminal sedation, euthanasia, physician assisted suicide and advocates respecting patient autonomy.
Professional practice level 4 assignment finalDave Manriquez
This document discusses ethical decision making and cultural considerations in healthcare using the case of a Korean patient, Mr. K.S. It notes that in Korean culture, the family does not want the patient to know their diagnosis due to beliefs that it could negatively impact their health. It analyzes this case using the CLPNBC Professional Standards and identifies both issues like lack of informed consent and potential solutions like providing interpreter services to overcome language and cultural barriers in patient care.
Dr. Aimee Thompson discusses the impact of childhood cancer on the family. To listen the audio recording, please visit: http://www.alexslemonade.org/campaign/symposium-childhood-cancer
Psychosocial aspects (Cancer patients has to cope with a variety of stressors)kalyan kumar
A diagnosis of cancer begins a long journey that can affect physical health, mental well-being, and relationships with loved ones. While getting treatment for the physical aspects of cancer, patients should not neglect the emotional issues associated with cancer. One of the best things patients can do to improve their quality of life is to learn more about their cancer. This can make the disease seem less mysterious and frightening. Information from your doctor and other credible sources can be very helpful in this respect.
The lecture I gave for the Indiana University Health Joint Transplant Education and Research Lecture Series on palliative care. That's right, palliative care in transplant patients NOT at the end-of-life.
This document discusses ethics and interventions for pain management. It acknowledges biases around pain management and explores themes in acute, chronic, and palliative pain settings. The four principles of ethics - autonomy, beneficence, non-maleficence, and justice - are applied to clinical cases. The principle of double effect and limits to intervention are also examined. Effective pain management is framed as a moral duty to relieve suffering.
This document discusses the basic principles of palliative care, including definitions, goals, ethical issues and barriers. It provides statistics on palliative care needs in Palestine, including causes of death, cancer rates and lack of services. Recommendations are made to establish national palliative care policies and programs, train healthcare workers, ensure availability of pain medications, and incorporate palliative care into existing healthcare systems to improve end of life care.
End of life decision making and approaches to issues of futility power point Bernard Freedman
This document summarizes key topics related to end-of-life decision making, including:
1) Ethically sound and legally mandated end-of-life decisions as well as the responsibilities of surrogate decision makers.
2) What constitutes futile care and how to deal with cultural and religious needs in end-of-life care.
3) The importance of documenting end-of-life decisions in the medical record and giving patients and surrogates sufficient information to make informed decisions.
This document discusses palliative care in the pediatric setting. It begins by outlining the epidemiology of childhood death, noting that over 55,000 children under 19 die annually in the US from a diverse set of causes including injuries, cancer, and complex chronic conditions. The goals and focus of palliative care are then described, emphasizing active total care to improve quality of life for patients and their families. Five principles of pediatric palliative care are discussed, including respect for patients/families, access to compassionate care, family support, advancement through research/education, and overlapping curative and comfort-focused care. Common symptoms experienced by children at end of life like pain, fatigue and dyspnea are also reviewed.
The document discusses a study on the lived experiences of pediatric cancer patients in the Philippines. It aims to understand their perceptions of cancer, how they cope with the disease, and what motivates them. The study found that the patients' perceptions centered around darkness and fear of death. Their coping mechanisms were influenced by changes in self, family, and their environment. Their main motivations came from the support of people around them, who gave them hope and encouragement. The conclusions state that the experiences and feelings of the cancer warriors should not be disregarded as they provide authentic insights into dealing with the disease. It recommends nursing practices and education incorporate a deeper understanding of the patients' perspectives.
Hospice care and palliative care: Is there a difference between the two, and if so, what?
Many people still think that palliative care means hospice care. But today, hospice is only a small part of palliative care.
The goal of palliative care is to prevent or treat the symptoms and side effects of a disease; and it should be part of the picture from the first day a serious illness is diagnosed.
Dr. Jim Meadows, Director of Hospice and Palliative Care at Tennessee Oncology, will discuss this important topic. How does a family and a health care team best work together to guide a patient through a terminal illness? How does everyone continue to support quality, patient-centered, end-of-life care?
The document provides information on palliative care, including:
- Palliative care aims to improve quality of life and relieve suffering for patients with life-limiting illnesses and their families.
- It focuses on pain management and other symptom relief without hastening or postponing death.
- Palliative care is appropriate at any stage of illness and can be provided alongside curative treatment.
The document summarizes areas for improvement in surgical efficiency, including ensuring on-time surgery start times, having the necessary tools available, and minimizing room turnover time between cases. It recommends having patients arrive earlier and being prepared when an OR becomes available, keeping all needed tools in the OR to avoid delays, and using two ORs that allow the surgeon and PA to work simultaneously between cases. Implementing these changes could increase the daily case volume and reduce wait times for patients and staff.
Palliative Care What Is Palliative MedicineIndranil Khan
This document provides information about palliative care from Dr. Indranil Khan, a palliative care provider in Kolkata, India. It defines palliative care as a holistic approach to improving quality of life for patients with chronic or life-threatening illnesses and their families through management of physical, psychological, social and spiritual problems. It outlines who can benefit from palliative care, the dimensions of care provided, components of care like home visits and access to pain medications, the multidisciplinary palliative care team, and common myths about palliative care.
Ethics presentation given at Providence Health Care on 2/19/16 as a part of a day-long nursing oncology conference. Discusses the fundamental clinical ethics consultation approach and discusses in narrative the relevant ethics cases that are common to oncology practice
Presented at Kansas City University of Osteopathic Medicine 10/27/15 in Lecture Series in Bioethics. See live presentation here: https://www.youtube.com/watch?v=Dr3g3PeVKeo
This document discusses hospice and palliative care. It begins by stating some key facts about death and the needs of dying patients. It then discusses why palliative care is needed to relieve suffering at the end of life. Palliative care aims to provide physical, psychological, social and spiritual support for patients and their families. The document outlines some obstacles to palliative care, such as delays in decision making and lack of resources and facilities. It compares the hospice approach, which specializes in end-of-life care, to the palliative care approach. The document argues that hospice may be better suited than palliation for Iraq due to its focus on minimizing costs, accommodating cultural needs, and being cost
Ethical, moral and legal issues in oncologyManali Solanki
The document discusses end of life care and ethics in oncology nursing. It defines end of life care as treating, comforting, and supporting those living with or dying from chronic life-threatening illnesses. It also discusses the importance of communication, education, and addressing spiritual-psychosocial needs of dying patients and their families. The document outlines several ethical issues that may arise in end of life care, such as medical futility, terminal sedation, euthanasia, physician assisted suicide and advocates respecting patient autonomy.
Professional practice level 4 assignment finalDave Manriquez
This document discusses ethical decision making and cultural considerations in healthcare using the case of a Korean patient, Mr. K.S. It notes that in Korean culture, the family does not want the patient to know their diagnosis due to beliefs that it could negatively impact their health. It analyzes this case using the CLPNBC Professional Standards and identifies both issues like lack of informed consent and potential solutions like providing interpreter services to overcome language and cultural barriers in patient care.
Dr. Aimee Thompson discusses the impact of childhood cancer on the family. To listen the audio recording, please visit: http://www.alexslemonade.org/campaign/symposium-childhood-cancer
Psychosocial aspects (Cancer patients has to cope with a variety of stressors)kalyan kumar
A diagnosis of cancer begins a long journey that can affect physical health, mental well-being, and relationships with loved ones. While getting treatment for the physical aspects of cancer, patients should not neglect the emotional issues associated with cancer. One of the best things patients can do to improve their quality of life is to learn more about their cancer. This can make the disease seem less mysterious and frightening. Information from your doctor and other credible sources can be very helpful in this respect.
The lecture I gave for the Indiana University Health Joint Transplant Education and Research Lecture Series on palliative care. That's right, palliative care in transplant patients NOT at the end-of-life.
This document discusses ethics and interventions for pain management. It acknowledges biases around pain management and explores themes in acute, chronic, and palliative pain settings. The four principles of ethics - autonomy, beneficence, non-maleficence, and justice - are applied to clinical cases. The principle of double effect and limits to intervention are also examined. Effective pain management is framed as a moral duty to relieve suffering.
This document discusses the basic principles of palliative care, including definitions, goals, ethical issues and barriers. It provides statistics on palliative care needs in Palestine, including causes of death, cancer rates and lack of services. Recommendations are made to establish national palliative care policies and programs, train healthcare workers, ensure availability of pain medications, and incorporate palliative care into existing healthcare systems to improve end of life care.
End of life decision making and approaches to issues of futility power point Bernard Freedman
This document summarizes key topics related to end-of-life decision making, including:
1) Ethically sound and legally mandated end-of-life decisions as well as the responsibilities of surrogate decision makers.
2) What constitutes futile care and how to deal with cultural and religious needs in end-of-life care.
3) The importance of documenting end-of-life decisions in the medical record and giving patients and surrogates sufficient information to make informed decisions.
This document discusses palliative care in the pediatric setting. It begins by outlining the epidemiology of childhood death, noting that over 55,000 children under 19 die annually in the US from a diverse set of causes including injuries, cancer, and complex chronic conditions. The goals and focus of palliative care are then described, emphasizing active total care to improve quality of life for patients and their families. Five principles of pediatric palliative care are discussed, including respect for patients/families, access to compassionate care, family support, advancement through research/education, and overlapping curative and comfort-focused care. Common symptoms experienced by children at end of life like pain, fatigue and dyspnea are also reviewed.
The document discusses a study on the lived experiences of pediatric cancer patients in the Philippines. It aims to understand their perceptions of cancer, how they cope with the disease, and what motivates them. The study found that the patients' perceptions centered around darkness and fear of death. Their coping mechanisms were influenced by changes in self, family, and their environment. Their main motivations came from the support of people around them, who gave them hope and encouragement. The conclusions state that the experiences and feelings of the cancer warriors should not be disregarded as they provide authentic insights into dealing with the disease. It recommends nursing practices and education incorporate a deeper understanding of the patients' perspectives.
Hospice care and palliative care: Is there a difference between the two, and if so, what?
Many people still think that palliative care means hospice care. But today, hospice is only a small part of palliative care.
The goal of palliative care is to prevent or treat the symptoms and side effects of a disease; and it should be part of the picture from the first day a serious illness is diagnosed.
Dr. Jim Meadows, Director of Hospice and Palliative Care at Tennessee Oncology, will discuss this important topic. How does a family and a health care team best work together to guide a patient through a terminal illness? How does everyone continue to support quality, patient-centered, end-of-life care?
The document provides information on palliative care, including:
- Palliative care aims to improve quality of life and relieve suffering for patients with life-limiting illnesses and their families.
- It focuses on pain management and other symptom relief without hastening or postponing death.
- Palliative care is appropriate at any stage of illness and can be provided alongside curative treatment.
The document summarizes areas for improvement in surgical efficiency, including ensuring on-time surgery start times, having the necessary tools available, and minimizing room turnover time between cases. It recommends having patients arrive earlier and being prepared when an OR becomes available, keeping all needed tools in the OR to avoid delays, and using two ORs that allow the surgeon and PA to work simultaneously between cases. Implementing these changes could increase the daily case volume and reduce wait times for patients and staff.
Kourtney Bowyer discusses ways to improve an urgent care center. The urgent care aims to provide convenient care for a variety of patients and help them between regular visits. The document recommends improving patient care through ensuring confidence in providers and proper fittings, improving efficiency through coordinated staff roles, and improving administration through organized patient tracking. It also stresses the importance of marketing the urgent care to local schools and communities to distinguish it from other centers.
This very short document appears to be in an unknown language or code and does not provide any discernible information to summarize in 3 sentences or less. It contains unrecognizable characters and words.
1) The document discusses the key concepts and objectives of an investment grade solar system feasibility study, including quantifying demand, balancing the value stack against the cost stack, and harvesting system design.
2) It outlines a 12-step process for conducting a feasibility study, from identifying the host customer and site to risk factors, capitalization, permitting, construction, and operations.
3) The goals are to get to feasible projects faster by leveraging tax incentives, technology, and customer needs, and to build projects that are right-sized and capitalized for success.
Holly went to the park on a sunny Saturday afternoon. She saw many people enjoying themselves and decided to join some children playing tag. After running around with the kids for a while, Holly felt tired but happy from the exercise and fun social interaction in the park.
Thesis Capstone Project (Spring 2016)- The Process of Spiritual Development a...Kayla Bass
This document discusses the process of spiritual development and inner healing prayer in the local church. It begins by defining spiritual development as a process of sanctification with the goal of union with Christ. It explores the stages of spiritual development according to John of the Cross (purgation, illumination, union) and Teresa of Avila's focus on the interior life of the soul and transformation through prayer. The document argues that inner healing prayer is important for the church to lead believers into deeper intimacy with God and addresses how psychological transformation relates to spiritual development. Overall, it presents spiritual development as a holistic process of transformation on individual and communal levels.
E-Bike Telematics - Final MBA Capstone PresentationNils Niederheide
Final presentation of my MBA capstone defending about "E-bike Telematics" - The integration of information and communications technology (ICT) into electric bicycles will create a new generation of connected e-bikes that offer totally new product benefits but also new business opportunities for the bicycle industry.
This document discusses cardiac rehabilitation and the effects of exercise. It describes 3 phases of cardiac rehabilitation: phase I focuses on early ambulation and low-intensity activities in the hospital; phase II involves incremental physical activity as an outpatient; and phase III emphasizes long-term community-based or home-based exercise. The benefits of habitual physical activity and exercise are summarized, including increased cardiac output and reduced heart rate, blood pressure, and mortality risks. Contraindications for exercise are also outlined.
This document provides information about cardiac rehabilitation, including indications, contraindications, risk factors, benefits of exercise, and phases of rehabilitation. It indicates that cardiac rehab is indicated for conditions like heart attack, angina, heart surgery, and heart failure. Contraindications include uncontrolled arrhythmias or blood pressure. Benefits of exercise include reduced risk of heart disease. Cardiac rehab occurs in phases from inpatient to lifelong maintenance and focuses on exercise based on metabolic equivalents of tasks.
This is a Feasibility Study conducted by a group of students "The Incorporators" from Capitol University's Bachelor of Science In Business Administration major in Marketing Management and Human resource Management.
Note: This document is not available to download, sorry for the inconvenience.
This document provides an introduction to the book "Cardiac Rehabilitation: A Guide to Practice in the 21st Century". It summarizes that the book provides an updated resource on cardiac rehabilitation practice based on scientific research since 1995. It translates scientific recommendations into practical applications to improve the quality of cardiac rehabilitation. The intended audience includes cardiologists, surgeons, physicians and other healthcare professionals who can refer patients to these important secondary prevention services.
Feasibility Study: Marketing , Technical and Management AspectLena Argosino
This document provides an overview of key considerations for the marketing and technical aspects of a business plan. It discusses conducting demand analysis to identify target markets and competitors. Product description, industry profile, demand segmentation, supply analysis, and marketing strategies are covered. For technical aspects, it outlines examining the production process, equipment needs, facility requirements, capacity, and operating costs. Organization and management factors like business structure and staffing are also mentioned.
This document discusses project planning and feasibility studies. It provides details on the importance of project planning, the basic components of a project plan, and the project planning process which involves 20 steps such as developing the project management plan, collecting requirements, defining the scope, and planning risk management. It also discusses what a feasibility study entails, including examining the market, organizational/technical, and financial aspects of a proposed project to determine its viability before significant resources are invested. A feasibility study aims to identify any issues that could prevent a project from being successful in the marketplace.
This feasibility report analyzes a proposed waste water system project. It recommends the project proceed based on identified needs in the community and project viability. Key points include: the existing system is deficient; a new system is needed to serve current and projected population; and the estimated capital costs and financing plan make the project economically feasible. The report provides background on the area's needs, outlines the proposed system components, and recommends next steps for further investigation and implementation.
This document outlines objectives and approaches for teaching cross-cultural geriatrics. It discusses the importance of cultural competence in healthcare and providing care tailored to individual needs and circumstances. Key topics covered include defining culture, relevant cultural constructs, challenges of cross-cultural care, content areas like explanatory models and alternative healing, case examples, and mnemonics and frameworks for cultural interactions. A variety of training tools and resources are presented, including large group exercises, small group activities, and references materials.
The document provides information on the Amish culture, including their origins in 16th century Switzerland, migration to the US in the 18th century, and lifestyle beliefs centered around their religious faith. It discusses Amish demographics, health risks such as genetic disorders and accidents, and their healthcare beliefs which incorporate alternative and complementary methods before seeking medical intervention. The document also outlines strategies for providing culturally competent care to the Amish community and challenges healthcare providers may face, such as language barriers and prejudice.
Prepared by louise kaplan, ph d, arnp, fnp bc, faanp senior pamit657720
This document provides a framework for critiquing research studies. It outlines 14 key aspects of a research article to evaluate, including the title, abstract, introduction, literature review, methods, analysis, results, discussion, limitations and conclusion. It recommends determining the level and quality of evidence using an appropriate scale. Finally, it asks the reader to decide if the study is applicable to their own practice. The overall purpose is to provide guidance on thoroughly reviewing and assessing the strengths and weaknesses of a research article.
This document discusses strategies for effectively addressing challenges presented by multi-cultural medical learners. It recognizes that learners come from diverse cultural backgrounds that can influence their medical education. The document provides an overview of cultural factors that may impact areas like patient care, career satisfaction, and community integration. It advocates developing curriculum that acknowledges these differences and assesses learners' experiences in a culturally sensitive manner.
The document discusses strategies for improving diabetes management programs to better serve racially and ethnically diverse patient populations. It emphasizes the importance of cultural competence and addressing health beliefs, alternative treatments, language barriers, and family roles that are specific to different ethnic groups. Effective programs elicit patients' cultural health beliefs, educate practitioners, provide language assistance, and address social factors like racism that can influence health outcomes.
Salon 2 15 kasim 11.00 12.00 nuran aydin-ingtyfngnc
The document discusses the importance of cultural competency in nursing care. It notes that culture shapes individuals' experiences, perceptions, and decisions. Providing culturally sensitive care requires understanding how culture influences health beliefs, behaviors, and patient-provider relationships. The best solution is for healthcare professionals to become culturally competent by developing knowledge of different cultural groups, skills in cross-cultural communication and patient-centered care, and awareness of one's own cultural values. Ongoing training and education can help improve cultural competency and lead to better patient outcomes and satisfaction.
This document discusses the importance of cultural competency in healthcare. It defines culture and cultural competency, and notes that the US population is becoming more diverse. It also discusses how minorities experience greater health disparities due to socioeconomic disadvantages and access to care issues. The document then outlines the commitment of Schwab Rehabilitation Hospital to diversity, inclusion, and providing culturally competent care. It discusses challenges like language barriers, biases, and microaggressions, and emphasizes the importance of education and training to improve cultural competency among healthcare providers.
This document provides an introduction to palliative nursing care. It defines palliative care as an approach that improves quality of life for patients with life-threatening illnesses through pain management and treatment of physical, psychosocial, and spiritual problems. Palliative care aims to prevent and relieve suffering. It has developed since the 1960s in the UK and US and is now integrated into health care systems worldwide. Palliative care can benefit those with advanced diseases, uncertain medical goals, or end-of-life care needs. Effective palliative care is patient-centered, family-supported, communicates effectively, and works with an interdisciplinary team. Barriers to palliative care include cultural views of death and lack of understanding, knowledge, communication skills
This document is a dissertation submitted by Amanda Elder to the Wright Institute Graduate School of Psychology in partial fulfillment of the requirements for the degree of Doctor of Psychology. The dissertation sought to enrich the understanding of older transgender individuals' subjective experiences in psychotherapy throughout their lifespan. Elder conducted interviews with 9 transgender-identified participants ages 60-83 to discuss their significant psychotherapy experiences. A qualitative thematic analysis was used to identify themes in the data. The dissertation aimed to offer perspectives on psychotherapy experiences that are often overlooked due to transgender marginalization and to improve psychotherapeutic care for gender variant people.
Depression Treatment 1Running head DEPRESSION TREATMENT IN .docxhallettfaustina
Depression Treatment 1
Running head: DEPRESSION TREATMENT IN AFRICAN AMERICAN BY CLERGY
DEPRESSION TREATMENT IN AFRICAN AMERICAN BY CLERGY 2
Depression Treatment in African American by Clergy
University Of Texas Arlington
Depression Treatment in African American by Clergy
Depression Treatment
The perception of clergy as the bridge to God along with cultural barriers results in the shunning of mental health professionals for the treatment of depression among the African Americans (Smith & Cummins, 2017). Although depression chronicity is higher among African Americans (56.5%) compared to whites (38.6%), 63% of the Black Community believe that depression is a personal weakness with nearly two-thirds agreeing that it can be addressed through prayers. Additionally, studies reveal that nearly 40% of African Americans rely on clergy for mental issues (Taylor, Sullivan, & Kliewer, 2013). Despite the high percentage of severity and high dependency on religious leaders, less than half of the clergy have training in counseling. As an illness, depression is treatable through medication, psychotherapy or a combination of both. Evidently, the clergy has a role to play in reducing the chronicity of depression among the Black Community by drawing a thick line between their religious and counseling duties. The clergy ought to recommend depressed congregants to mental professionals if the symptoms exhibited by individuals are beyond their mandate (Taylor, Sullivan, & Kliewer, 2013). So, how does liaising with health professionals or getting more information on depression help in reducing the chronicity of depression among the African Americans?
After approval by the Institutional Research Review Board of the University of Cincinnati, Anthony, Johnson, & Schafer (2015) conducted research to examine the role of clergy and church in the treatment of depression among the African Americans. The research targeted 18-year-old or older African American clergy with the ability to read and complete the data collection tools. Several notable facts emerged from the research that explores the treatment of depression among the Black Community through clergy services. The interviewed religious leaders spent 50-80% of their time counseling the congregants with the services starting with the children before evolving to the whole family (Anthony, Johnson, & Schafer, 2015). Additionally, educational levels of the clergy had a notable influence on the counseling services i.e. the higher the levels, the more likelihood of having a depressed and anxiety counseling training hence the better the services. Lastly, over 50% of the clergy believe that depression and spiritual counseling are similar hence high chances of employing spiritual services to address depression symptoms in patients. However, nearly all the clergy agreed that additional information on depression is essential in addressing this illness among their congregants.
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This document summarizes research on factors that predict and promote resilience in physically ill individuals. It finds that psychological factors like self-esteem, optimism, and mastery are associated with resilience. Effective coping strategies include spirituality, positive appraisal, and benefit finding. Social support from family and friends also predicts resilience. The document reviews studies on specific illnesses and interventions to increase resilience. It concludes that understanding resilience could help improve care and outcomes for physically ill patients.
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End-of-Life CareEnd-of-Life CareEnd-of-Life CareEnd-of-Life CareEnd-of-Life Care
WHAT ARE OLDER ADULTS’ MENTAL HEALTH NEEDS
NEAR THE END OF LIFE?
The US Supreme Court agreed that Americans should expect palliative care,
which combines active and compassionate therapies to comfort and support
individuals and families nearing the end of life. End of life is defined as that
time period when health care providers would not be surprised if death
occurred within about 6 months. Older Americans with chronic illness think
about how they would prefer their lives to end, and want a “good death”
without burdensome pain, symptoms and technology.
Most deaths (70%) occur in those aged 65 and older. Older adults want better discussions,
information, and a chance to influence decisions about their care—whether to be at home
or in the hospital and to have CPR (cardiopulmonary resuscitation) (Foley, 1995). Most
Americans die in hospitals (63%), and another 17% die in institutional settings such as
long-term care facilities (Foley, 1995; Isaacs & Knickman, 1997). In addition, most
people are referred too late to hospice or palliative care, so they are unable to get the most
benefit possible from these specialized services.
WHAT DO OLDER ADULTS FEAR MOST?
People fear that their pain, symptoms, anxiety, emotional suffering, and family
concerns will be ignored. Many critically ill people who die in hospitals still receive
unwanted distressing treatments and have prolonged pain. Many fear that their
wishes (advance directives) will be disregarded and that they will face death alone
and in misery. Physicians may use confusing or vague medical terms and talk briefly
about treatment options when the patients are too sick to participate. Most people
want to discuss advance directives when they are healthy and often want their
families involved.
Caregivers reported that a third of 1227 elderly individuals were in unnecessary pain
during the 24 hours before their death. Studies show that two thirds of elderly patients have
pain in the last month of life (Foley, 1995). Although palliative/comfort care could relieve
most of this pain and suffering, patients typically spend 8 days in ICU (an intensive care
unit) comatose or on a ventilator and 30% of patients spend at least 10 days in ICU
before they die (Isaacs & Knickman, 1997).
When discussing a good end of life with a patient, physicians in one study talked about 5-6
minutes, spoke for 2/3 of this time, and did not consider the patient’s values or preferences
(Tulsky, Fischer, Rose & Arnold, 1998). If patients were too sick to make decisions, most
wanted their family to be given choices about treatment and only 41% wanted the
physician to make treatment decisions without consulting them. In 91% of cases in which
physicians discussed end of life treatment options, they did so in scenarios in which most
patients would not want to be treated, whereas o ...
This document discusses the need to broaden advance care planning beyond advance directives and focus more on preparing patients and their surrogates for medical decision making through communication. It notes that traditional advance directives often do not improve outcomes and can cause stress. Research identified 5 key behaviors to prepare for decision making: 1) Choosing a surrogate, 2) Reflecting on values and priorities, 3) Discussing flexibility for the surrogate, 4) Informing family/doctors of decisions, and 5) Asking clinicians about treatment outcomes. The PREPARE website was created to model and teach these behaviors through videos and improve engagement in the planning process. The field needs new outcomes measures that assess progress along the behavioral change pathway for multiple advance
Dignity therapy is a novel psychotherapeutic intervention designed to address psychosocial and existential distress in terminally ill patients. It involves conducting a recorded interview where patients discuss what matters most to them or what they want remembered. The recording is then edited into a "generativity document" that is given to the patient to share with loved ones. This study examined the feasibility and impact of dignity therapy on measures of distress in terminally ill patients.
The document discusses cultural considerations for end-of-life care among various ethnic groups. It aims to understand how culture affects medical care and decision making, and to learn about end-of-life traditions and beliefs in African Americans, Asian/Pacific Islanders, Latinos, and Native Americans. Key differences are noted in views on truth telling, technology use, and decision styles. Respecting cultural values is important for better clinical outcomes and care satisfaction.
Mary Ersek-Nursing Home-Based Palliative Care: Empowering Nurses as IDT Team ...jewishhome
This document provides an overview of a conference on integrating palliative care into nursing homes. It describes the growing elderly population in nursing homes, many of whom have advanced dementia or other serious illnesses. The document outlines the roles and responsibilities of different nursing home staff in delivering palliative care, including assessing symptoms, facilitating goals of care discussions, and offering bereavement support. It recommends strategies for preparing staff, such as educating them about palliative care principles and conducting skills assessments. The document also reviews ways to evaluate the quality of palliative care through structure, process and outcome measures.
The document provides a biography and overview of Madeleine Leininger's Theory of Transcultural Nursing. Some key points:
- Leininger observed differences in patient behaviors from diverse cultures and questioned how culture impacts care. This led her to establish the theory of culture care.
- The theory is based on the assumptions that care is essential to health and culture influences all aspects of life, including views of health and illness.
- Leininger developed the Sunrise Model and three care modalities to guide culturally congruent nursing care: preservation, accommodation, and repatterning.
- The goal of the theory is for nurses to incorporate a patient's cultural beliefs, values and preferences
PSY605 End-of-Life Case Scenarios Case 1 Roger is a healt.docxwoodruffeloisa
PSY605 End-of-Life Case Scenarios
Case 1: Roger is a healthy 62-year-old African American male with a wife and four grown children.
While out on his morning jog two weeks ago, he was hit by a drunk driver. Roger has been left paralyzed
from the neck down, and he is no longer able to perform basic life-sustaining functions such as eating or
breathing without the help of machines. Because he can no longer talk or use his hands to write, his
communication is limited to moving his head in simple “yes” or “no” responses when asked a question.
His living will was last updated 25 years ago when his youngest child was born. The will indicates that
Roger would like to receive life-saving treatments in these types of events. However, when prompted by
doctors, nurses, and the hospital-appointed social worker regarding his current wishes, he seems to be
communicating that he does not want to continue living in his current state.
Case 2: Geri is a 38-year-old single mother. Her son, Gabe, is 17 years old and a junior in high school.
After experiencing some headaches and changes in mood over the past several weeks, Geri finally visited
a neurosurgeon a week ago. During that visit, it was discovered that she has an inoperable brain tumor.
Her life expectancy is 6 to 8 months. In addition to fears about her own impending death, Geri is very
worried about how to best provide for and take care of her son. She cannot decide if she should continue
working full-time to make sure that Gabe’s expenses are taken care of, or if it is best to take this
remaining time off to enjoy with her son. Once she is gone, she does not know if she should send Gabe to
live with an aunt who lives several states away for his final year of high school, or if she should allow
him to live with a friend in their neighborhood and grant custody to that parent so Gabe could continue
living and going to school where he is most comfortable. She is also at a loss as to how to explain this
situation to Gabe in a way that he will understand so that both of them will be able to move forward.
Fact Sheet onFact Sheet onFact Sheet onFact Sheet onFact Sheet on
End-of-Life CareEnd-of-Life CareEnd-of-Life CareEnd-of-Life CareEnd-of-Life Care
WHAT ARE OLDER ADULTS’ MENTAL HEALTH NEEDS
NEAR THE END OF LIFE?
The US Supreme Court agreed that Americans should expect palliative care,
which combines active and compassionate therapies to comfort and support
individuals and families nearing the end of life. End of life is defined as that
time period when health care providers would not be surprised if death
occurred within about 6 months. Older Americans with chronic illness think
about how they would prefer their lives to end, and want a “good death”
without burdensome pain, symptoms and technology.
Most deaths (70%) occur in those aged 65 and older. Older adults want better discussions,
information, and a chance to influence decisions about their care—w ...
3. Norman
McRae
Founder of Caris Healthcare
“Near the end of life, Caris strives to
provide care to patients in the locale of
their preference by an interdisciplinary
team made up of a nurse, aide, social
worker, chaplain, and volunteer who are
all supervised by a physician and
supported by pharmacists and nurse
practitioners. Our goal is to provide
everyone who needs hospice an
experience that is grounded in
excellence by a team of caregivers who
are available when needed, day and
night, to respond with urgency.”
4. The
Better
Way
All are held to this standard
Explained to all patients and
families
Must be worn on badge
Signed certificate
5. Learning Objectives
1) To gain invaluable, practical counseling experiences that will be used as
preparation for graduate school and future employment.
2) To use the knowledge and techniques gathered and continued to be
gathered in the classes taught at Presbyterian College and apply them
in a practical, ethical way.
3) To expand my personal knowledge of other social, ethnic, and religious
practices other than my own to serve the clients of Caris Healthcare and
with future clients in graduate school and future employment with the
best care and understanding possible.
7. Patient Demographics
Six patients at NHC of Clinton
One in Langston Place
One at-home patient
One Male, Seven Females
Five Caucasian, Three African-American
Dementia, Heart Disease, Stroke
9. Why are Demographics
Important to Consider?
Cultural Considerations when “ADDRESSING” patients’ needs
Age & Generational Influences
Disabilities (Developmental)
Disabilities (Acquired)
Religion
Ethnic/Racial Identity
SES
Sexual Orientation
Indigenous Heritage
National Origin
Gender
(Magyar-Moe, 2009)
10. Does Being Culturally Aware Matter?
Sampled low-income African Americans
(n=110) and non-Hispanic White
Americans (n=119)
Correlational Study
Questionnaire measuring eight areas
Study Conducted: Patient-Centered Culturally Sensitive
Health Care: Model Testing and Refinement
(Tucker, Marsiske, Rice, Nielson & Herman, 2011)
11. Provider Cultural Sensitivity
African
American
White
Trust in Provider 0.548*** 0.823***
Satisfaction with
Care
0.725*** 0.789***
Health
Promoting
Lifestyle
0.238* 0.277**
(Tucker, Marsiske, Rice, Nielson & Herman, 2011)
RESULTS
Significant
correlation
*** p<.001
** p<.01
*p<.05
13. Religion
All of my patients identify
as Christian
All have this in some
aspect of Three Most
Important Things
Two are “new” Christians
14. Coincidence?
Do older people need God?
Church-based social support
Focus on African-Americans
Well-being with God-mediated control
Can conclusions be made about the sick?
(McFadden, 2005)
15. Biologically Inclined to
Believe?
Terror Management Theory
All humans are aware of death
Death knowledge causes great
anxiety
Managed by immersion
something deemed meaningful
(Rowatt, Shen, LaBouff, & Gonzalez, 2005)
16. Scared to
Death?
Osarchuk and Tatz
studied change in belief
in afterlife
Mortality salience led to
stronger religiosity
(Jost, Kay & Thorisdottir, 2009)(Norenzayan & Hansen, 2006)
19. Sandwich
Generation
They are responsible for all support
Financial Support
Children
Parents
Emotional Support
Children
Parents
People, typically in their thirties
or forties, responsible for raising
their children and caring for their
aging parents
(Parker & Patten, 2013)
20. (Parker & Patten, 2013)
Financial Stress and the Sandwich Generation
Q: How would you describe your household’s financial situation? (%)
Sandwich Generation
Supporting parent 65+ Not supporting parent 65+
Live comfortably 28 41
Meet basic expenses with a little left over 30 31
Just meet basic expenses 30 17
Don’t have enough to meet basic expenses 11 10
• Unpaid caregivers provide 90% of long-
term care
• $5,531 on average caring for
someone 50+
• Typical caregiver: 46 six year old, woman,
more than 20 hours of care
• 53% of caregivers report worsen health
• 67% do not go to the doctor for
family’s needs
21. What to do with this research
and these statistics?
Companies like Caris can use these
to better serve the patients and their
families.
Be culturally aware to for best patient
outcome
Encourage patients’ faiths for best quality
of end of life care
Encourage families
Cognitive care
Time off
Spiritual and cognitive family care
Post Presbyterian College Goals
Masters in Clinical Mental Health
Specialize in hospice/trauma counseling
Graduate thesis
Work with underserved populations
Galatians 5:13 “For you were called to
freedom, brothers. Only do not use your
freedom as an opportunity for the flesh,
but through love serve one another.”
22. Dr. Evelyn Hunter, Presbyterian College
Internship & Capstone Advisor
Lynn Downie, Presbyterian College
Internship Coordinator
Leigh Workman, Caris Healthcare
Volunteer Coordinator
24. References
1.Bevans, M. F., & Sternberg, E. M. (2012). Caregiving Burden, Stress, and Health
Effects Among Family Caregivers of Adult Cancer Patients. Jama, 307(4), 398–
403. http://doi.org/10.1001/jama.2012.29
2.Jost, J., Kay, A., & Thorisdottir, H. (2009). Social and psychological bases of ideology
and system justification. Oxford: Oxford University Press.
3.Krause, N. (2004). Common facets of religion, unique facets of religion, and life
satisfaction among older African Americans. Journal of Gerontology: Social Sciences,
59B, S109-S117.
4.Magyar-Moe, J. (2009). Therapist's guide to positive psychological interventions.
Amsterdam: Elsevier/Academic Press.
5.McFadden, S. H. (2005). Old Persons, Old Age, Aging, and Religion. In R. F.
Paloutzian & C. L. Park (Eds). Handbook of The Psychology of Religion and
Spirituality (pp.198-212). New York:The Guilford Press.
6.Morris, S. M., King, C., Turner, M., & Payne, S. (2015). Family carers providing
support to a person dying in the home setting: A narrative literature review. Palliative
Medicine, 29(6), 487-495. doi:10.1177/0269216314565706
7.Norenzayan, A., & Hansen, I. (2006). Belief in Supernatural Agents in the Face of
Death. Personality And Social Psychology Bulletin, 32(2), 174-
187. http://dx.doi.org/10.1177/0146167205280251
8.Parker, K., & Patten, E. (2013). The Sandwich Generation: Rising Financial Burdens
for Middle-Aged Americans. Pew Research Center. Retrieved 1 November 2015,
from http://www.pewsocialtrends.org/2013/01/30/the-sandwich-generation/
9.Rowatt, W. C., Shen, M. J., LaBouff, J. P., & Gonzalez, A. (2005). Religious
Fundamentalism, Right-Wing Authoritarianism, and Prejudice: Insights from Meta-
Analyses, Implicit Social Cognition, and Social Neuroscience. In R. F. Paloutzian & C.
L. Park (Eds). Handbook of The Psychology of Religion and Spirituality (pp.457-
475). New York:The Guilford Press.
10.Sue, D. (2015). Cultural Diversity and Microaggressions: Applications to
Counseling. Hoboken, NJ: John Wiley & Sons, Inc.
11.Tucker, C., Marsiske, M., Rice, K., Nielson, J., & Herman, K. (2011). Patient-
centered culturally sensitive health care: Model testing and refinement. Health
Psychology, 30(3), 342-350. http://dx.doi.org/10.1037/a0022967.
Editor's Notes
Caris is an acronym meaning: Compassion, Accountability, Respect, Integrity, and Service
This is the basis for the company in which all employees and volunteers must uphold not only for our patients, but for their families
“Caris” comes from the Greek word meaning ‘grace’
The vision and mission of the company embodies what Caris stands for and its origin
Vision: committed to being your world class hospice
We serve many patients and families, but we treat each patient as if they are our only one
The Power of One
Mission: Hospice care with grace
Statement from the founder:
“Near the end of life, Caris strives to provide care to patients in the locale of their preference by an interdisciplinary team made up of a nurse, aide, social worker, chaplain, and volunteer who are all supervised by a physician and supported by pharmacists and nurse practitioners. Our goal is to provide everyone who needs hospice an experience that is grounded in excellence by a team of caregivers who are available when needed, day and night, to respond with urgency.”
The Better Way is the way we hold ourselves accountable to provide the best services to patients and families
The Better Way is comprised of 20 “I promise to”
All promises must be carried out each day and when encounter every patient
All employees and volunteers have to pledge to uphold all of these promises and each receive a signed certificate
We must keep the promises (as employees) with us at all time as a reminder
There is a daily call for every office in the country from headquarters
Each morning there are real life examples of how different employees from different offices have upheld these promises
To gain invaluable, practical counseling expereinces that will be used as preparation for graduate school and future employment.
To use the knowledge and techniques gathered and continued to be gathered in the classes taught at Presbyterian College and apply them in a practical, ethical way.
To expand my personal knowledge of other social, ethinic, and religious practices other than my own to serve the clients of Caris Healthcare and with future clients in graduate school and future employment with the best care and understanding possible.
Learning objective #1 1 practical counseling skills
My position within the company was a patient volunteer
My main task is to visit with each patient
Pay special attention to the Patient’s 3 most important things
They can be anything and everything
One patient I pray with before I leave
Another is having her nails painted
Another is KFC chicken wings
Remembering the power of 1, I try to go above and beyond with my patients
Example: one of my patients turned 104
I brought her a birthday card and flowers
Her family was touched and even called the office for thanks
KOJO points are assigned when employees go above and beyond
The companies way of recognizing its employees and volunteers
I have to complete documentation each visit
This keeps me and the company accountable
I have to document the time I was there and what we did and how I included 3 most important things
Documentation has to be signed by either a nurse or caregiver (at home) for accountability
Accountability ensures that our patients get the best care
Going back to vision and mission
Six patients at NHC of Clinton
One in Langston Place
One at-home patient
One Male, Seven Females
Five Caucasian, Three African-American
Dementia, Heart Disease, Stroke
Learning Objective #3 – Learn about other ethnic, cultural issues
Addressing Model of Cultural Assessment
Developed by Pamela Hayes
Intended to help therapists conceptualize indignities across different dimensions
Completed inventory for me and for patient
Allows me to understand my own background that comes with beliefs and identity that may different than my patients
The areas in which I mostly different with at least one of my patients
Age (young vs. older)
Disabilities Later in life (including physical and cognitive/psychological)
Ethnicity
SES
Gender
I have to make myself aware of these differences so when I am with each patient, I am making sure that I am catering to their specific needs and not just what I assume or I think I would want
Example:
Most of my patients have lived through the roaring 20s and then through the great depression
Lived with technology advances that I take fore granted
Study published and accepted by US National Library of Medicine National Institutes of Health
Objective: Explain and improve health care for ethnically diverse patients seen in community-based primary care clinics
Total 229 participants
Areas included:
Provider cultural sensitivity
trust in provider
patient interpsonal control
patient satisfaction
physical stress
health promoting lifestyle
diet adherence
medication adherence
Significant correlation
*** p<.001
** p<.01
*p<.05
What does this mean?
- the study found support for a postive correlation
- The more the provider was cultural sensitive, there was a higher trust in provider, satisfaction with care, and having a health promoting lifestyle
“New” christians meaning that they are new in faith. Bot patients agreed that they always believed there was some sort of God but did not become believers until they became sick
Church-based support are associated with a sense of well being for the older adults, not necessarily sick adults
Study was on African American adults but found it to be true across all races
Another study showed that particularly in african american christians show better outcomes in well being when they embrace idea of God-mediated control
There needs to be more research, but it seems logically to hypothesize that the especially older, sick individuals use belief of God being in control
Religiosity is very important
Religion often buffers death anxiety
John 3:16
In participants, there was a greater change (more beleif) in the afterlife after the participants were exposed to Death threat condition
It is important to note that this study has not been replicated, however, it is often sighted as preliminary foundation for other studies
Mortality salience is when an individual becomes aware that his or her death is inevitable
Participants responded to 2 questions
How religious are you
How strongly do you believe in God
Death motivates religiosity, more specifically in a higher power
People, typically in their thirties or forties, responsible for raising their children and caring for their aging parents
Financial Stress
Live comfortably 28% as opposed to 41%
Meet basic expenses with a little left over 30 vs 31%
Just meet basic expenses 30 vs 17%
Don’t have enough to meet basic expenses 11 vs 10%
Unpaid caregivers provide 90% of long-term care
$5,531 on average caring for someone 50+
Typical caregiver: 46 six year old, woman, more than 20 hours of care
53% of caregivers report worsen health
67% do not go to the doctor for family’s needs