Writer Adam Baer in an op-ed on the pressure that medical patients feel to promise recovery. A call for health diversity and an understanding of health fluidity.
This power point contains some introduction information about what chronic pain is and is meant as an overview for people without chronic pain. It is meant for educational purposes and also contains information about societal biases towards chronic pain as disabilities and the emotional consequences of these prejudices.
The document discusses two recent studies on attitudes towards death and end-of-life discussions. The Co-operative Funeral Care report found that most people only think about their own mortality when prompted by external events like a family death or medical diagnosis. They also do not discuss death with others. Similarly, a Royal College of Physicians report found doctors have difficulty discussing death with patients, even more so than patients themselves. The document argues doctors have an important role in assisting families with practical and healthy end-of-life conversations to help reduce pain for all involved.
The document discusses the importance of providing end of life care and hospice options for patients. It notes that while most people prefer to die peacefully at home, currently less than 25% do. Hospice aims to give patients more control and choice over their end of life experience. The goals of hospice care include pain management, comfort, and supporting relationships at the end of life. Local organizations like Mary T. Hospice provide hospice services in homes, facilities, and offer information to help patients and their families.
This document discusses leukemia, a type of cancer that affects thousands of children each year in the United States. It primarily affects children between the ages of 3-15 and can drastically alter their lives. The disease involves an overproduction of abnormal, non-functioning blood cells which collect in the bone marrow and bloodstream. There are two forms, acute and chronic, with acute involving a more rapid overproduction of abnormal cells. Significant efforts have been made to research and cure leukemia through organizations like St. Jude Children's Research Hospital, founded by Danny Thomas in 1962 to support research for diseases that affect children. The hospital receives over $1 million in daily funding to support its facilities and treatment of over 5,000 patients at a time
This document provides a summary of the Spring 2015 issue of the Affinity Health System magazine. It discusses various ways that the health system focuses on healing, including cancer survivorship, neonatal intensive care, and living with rheumatoid arthritis. It also includes other short articles on topics like sleep health, volunteering, quinoa recipes, and the benefits of olive oil. The issue introduces the new president of St. Elizabeth Hospital and provides information about the organization's mission and values.
My mother was diagnosed with Alzheimer's disease in her 70s. [1] As her condition deteriorated, she could no longer be cared for at home and was placed in assisted living facilities, but these facilities were unable to properly care for her as her dementia progressed. [2] Alzheimer's patients and their families face immense financial and emotional burdens, as the cost of long-term care is not covered by Medicare and facilities are ill-equipped for end-stage patients. [3] The author calls for policy changes to help address the inadequate support systems and the tremendous challenges of Alzheimer's disease.
Heart Disease is the Number One Killer of WomenJulie Correll
Heart disease is the number one killer of women. The symptoms of a heart attack, such as sweating, pressure, nausea and jaw pain, are often dismissed by women as less serious issues. A strategic communication campaign is proposed for Franciscan St. Elizabeth Health Hospital to raise awareness of women's heart health issues throughout the year, not just in February which is National Heart Month. The campaign would utilize various outreach and fundraising events to educate the local community about risk factors and symptoms of heart disease.
This document discusses vasculitis, a group of rare diseases that cause inflammation of the blood vessels. It describes one patient's experience with Behcet's Disease, a type of vasculitis, including their symptoms since age 13, diagnosis at age 34, and failed treatment attempts. The patient expresses 3 wishes: 1) more understanding from medical professionals and society about chronic illnesses, 2) to remove the anguish experienced by patients and their families, and 3) to have support centers similar to Maggie's Centers for cancer patients, which provide practical advice, emotional support, and a community for rare disease patients.
This power point contains some introduction information about what chronic pain is and is meant as an overview for people without chronic pain. It is meant for educational purposes and also contains information about societal biases towards chronic pain as disabilities and the emotional consequences of these prejudices.
The document discusses two recent studies on attitudes towards death and end-of-life discussions. The Co-operative Funeral Care report found that most people only think about their own mortality when prompted by external events like a family death or medical diagnosis. They also do not discuss death with others. Similarly, a Royal College of Physicians report found doctors have difficulty discussing death with patients, even more so than patients themselves. The document argues doctors have an important role in assisting families with practical and healthy end-of-life conversations to help reduce pain for all involved.
The document discusses the importance of providing end of life care and hospice options for patients. It notes that while most people prefer to die peacefully at home, currently less than 25% do. Hospice aims to give patients more control and choice over their end of life experience. The goals of hospice care include pain management, comfort, and supporting relationships at the end of life. Local organizations like Mary T. Hospice provide hospice services in homes, facilities, and offer information to help patients and their families.
This document discusses leukemia, a type of cancer that affects thousands of children each year in the United States. It primarily affects children between the ages of 3-15 and can drastically alter their lives. The disease involves an overproduction of abnormal, non-functioning blood cells which collect in the bone marrow and bloodstream. There are two forms, acute and chronic, with acute involving a more rapid overproduction of abnormal cells. Significant efforts have been made to research and cure leukemia through organizations like St. Jude Children's Research Hospital, founded by Danny Thomas in 1962 to support research for diseases that affect children. The hospital receives over $1 million in daily funding to support its facilities and treatment of over 5,000 patients at a time
This document provides a summary of the Spring 2015 issue of the Affinity Health System magazine. It discusses various ways that the health system focuses on healing, including cancer survivorship, neonatal intensive care, and living with rheumatoid arthritis. It also includes other short articles on topics like sleep health, volunteering, quinoa recipes, and the benefits of olive oil. The issue introduces the new president of St. Elizabeth Hospital and provides information about the organization's mission and values.
My mother was diagnosed with Alzheimer's disease in her 70s. [1] As her condition deteriorated, she could no longer be cared for at home and was placed in assisted living facilities, but these facilities were unable to properly care for her as her dementia progressed. [2] Alzheimer's patients and their families face immense financial and emotional burdens, as the cost of long-term care is not covered by Medicare and facilities are ill-equipped for end-stage patients. [3] The author calls for policy changes to help address the inadequate support systems and the tremendous challenges of Alzheimer's disease.
Heart Disease is the Number One Killer of WomenJulie Correll
Heart disease is the number one killer of women. The symptoms of a heart attack, such as sweating, pressure, nausea and jaw pain, are often dismissed by women as less serious issues. A strategic communication campaign is proposed for Franciscan St. Elizabeth Health Hospital to raise awareness of women's heart health issues throughout the year, not just in February which is National Heart Month. The campaign would utilize various outreach and fundraising events to educate the local community about risk factors and symptoms of heart disease.
This document discusses vasculitis, a group of rare diseases that cause inflammation of the blood vessels. It describes one patient's experience with Behcet's Disease, a type of vasculitis, including their symptoms since age 13, diagnosis at age 34, and failed treatment attempts. The patient expresses 3 wishes: 1) more understanding from medical professionals and society about chronic illnesses, 2) to remove the anguish experienced by patients and their families, and 3) to have support centers similar to Maggie's Centers for cancer patients, which provide practical advice, emotional support, and a community for rare disease patients.
This document discusses how people with dementia and their families cope with bereavement and loss. It notes that grief can be a disenfranchised or ambiguous experience for those with dementia as they may forget losses or confuse past and present. Expressions of grief in dementia can include agitation, distress, or confusion about a missing person. It emphasizes the importance of person-centered care, reminiscence work, honesty and consistency when supporting those grieving with dementia.
Error is almost inevitable in our clinical practice so we should be prepared to help and prepare those individuals involved for the benefit of them, our systems and our patients.
Do you remember that patient you saw last night?': A phrase the strikes terror into the hearts of all physicians. The prospect of a patient coming to harm as a result of a mistake is terrifying but it can and does happen.
The consequences for the patient and their family are often tragic but what of the clinicians who made the error? For many the result of making a terrible error is life changing.
Those permanently harmed by error are often referred to as second victims with the consequences of terrible events being life-long.
This talk explores the predictable course for clinicians who are involved in error and asks whether we can prepare and support such individuals through a difficult time.
Cultural Competence in Palliative CareLinda Golley
The document discusses cultural considerations in palliative care, including goals, needs, and preferences of patients from different cultural backgrounds. It provides scenarios of palliative care patients with cultural issues related to decision making, family dynamics, religious beliefs, and expectations around independence. Keys to understanding a patient's cultural context include asking the patient directly, using knowledge of their world and life experiences, and paying attention to non-verbal cues and behaviors.
Ambiguous Loss Supporting families with missing loved onesMaureen Trask
Nov. 7, 2017 presentation to the Volunteers of Victim Services Wellington about Ambiguous Loss to support families with missing loved ones. Presented by Maureen Trask.
Donald Vincent Moncrief has worked for the United States Marine Corps, the San Diego Police Department, the Pugilistic Offensive Warrior Tactics, Eastlake Elementary School, and Rady Children’s Hospital.
Due in an effort to facilitate scholarly discourse, create yourronak56
The video discusses barriers to mental healthcare in communities of color. It profiles Toy Burton who started an organization called DeeDee's Cry after her sister died by suicide. The video highlights stigma, lack of representation in the mental healthcare field, socioeconomic barriers, and mistrust of doctors as barriers. It suggests increasing representation of people of color as therapists and addressing stereotypes to improve access.
The author discovered an opportunity to volunteer with the Global Medical Foundation in the Philippines through an American College of Surgeons website. This fulfilled a promise the author made 11 years earlier to return to the Philippines as a physician. Volunteering has given the author perspective on their own career and inspired gratitude for resources available in the United States. Performing surgeries in challenging conditions in other countries renews the author's passion for medicine. Volunteering has become an essential part of the author's medical career to find purpose and overcome challenges.
La health examiner erica ives - shapiro pr - march 2013Kelila Shapiro
The document discusses eating disorders and a therapist's new book on the topic. It notes that over 10 million Americans suffer from anorexia or bulimia, which are the two most common eating disorders. The therapist, Erica Ives, has suffered from and recovered from an eating disorder herself. Her book aims to educate readers on what eating disorders look like and how to help those suffering from them. Ives notes that eating disorders allow people to communicate feelings they can't express otherwise, and that expanding knowledge of the disorders can help identify early signs and support recovery.
The document discusses how perceptions of women's mental states negatively impact the diagnosis and treatment of heart disease. Both female patients and doctors are less likely to pursue aggressive treatment for heart symptoms in women. While heart disease presents differently in women, the medical field still follows a male-centered model. Changing these perceptions will require education about women's heart risks, creating unity among women's health advocates, and allowing more women to participate in medicine.
Mr. Thavamani was paralyzed from the waist down due to demyelinating polyneuropathy. He was depressed and in severe pain, and had lost hope for his future. Through regular visits from a medical team, physiotherapy, counseling, assistive devices, and community support, his confidence increased. He learned to stand independently with support and is working towards walking again and returning to his daily life activities.
In Conversation with Compassion and Care
Concern to ensure compassion and empathy are core experiences in care services are now a priority following appalling scandals in care homes and hospital settings. Of course, at a time of economic austerity and threats to health and social services, caring about those in socially excluded groups seems to be less of a priority for governments, national and local. Improving the health and wellbeing of the population at large is one approach to this that is creating a more compassionate and caring society, within which all citizens can expect fair treatment and supportive concern when they face hard times.
However, these aspirations then beg the question, why do we not have compassionate care in care services, and why is society no longer, or no more compassionate. This series of short essays from experts is refreshing and thought provoking. There is depth in the experiences that are shared, some intimate some heartbreaking. careif is planning to provoke more conversations in compassion and care, so please share with others and send your views/essays to enquiries@careif.org
http://www.careif.org/knowledge/commentary-and-analysis.html
The document discusses coping with loss and grief, explaining that understanding the grieving process helps manage feelings in a healthy way. It describes the stages of grief, including denial, anger, bargaining, depression, and acceptance. Finally, it emphasizes that support from others and the community is important for coping with loss, death, and traumatic events.
The document discusses physician burnout and argues that organizing toward collective action can help address burnout caused by feelings of powerlessness when treating patients facing socioeconomic hardships. It notes that while burnout is usually attributed to work overload and bureaucracy, its origins may also lie in caring for marginalized patients whose health issues stem from deep-rooted social problems beyond a physician's control. Organizing with others around such issues can combat isolation and empower physicians to enact meaningful change, providing a strategic and therapeutic approach to fighting burnout.
The document provides an agenda and background information for a workshop on metastatic colorectal cancer (mCRC) patient journeys. The workshop aims to illuminate the patient experience, explore barriers to third and fourth line treatment, identify solutions to barriers, and generate support/adherence ideas. The methodology section outlines that the workshop will involve gathering existing knowledge, discussions with medical professionals, sharing early insights and a draft journey map, conversations with patients and caregivers, input from a behavioral psychologist, and an insights presentation and innovation session. Key overarching insights from patient interviews include that mCRC changes people, it's difficult to talk about colon/rectal issues, patients feel a loss of power, and patients maintain hope despite their situation
1) Charlie, a respected orthopedist and mentor of the author, was diagnosed with pancreatic cancer but refused all treatment and focused on spending time with family, eventually dying at home.
2) Doctors experience death differently than most - they are aware of medical limitations and options and generally have a serene acceptance when facing their own mortality, opting for minimal treatment and dying peacefully.
3) The author argues that the medical system encourages excessive treatment out of fear of litigation and desire to avoid blame, even when treatment provides only misery, and that doctors still refuse such treatment for themselves by focusing on dignity and quality of life over aggressive measures near the end.
Annals of Surgery and Perioperative Care is an open access, peer reviewed, scholarly journal dedicated to publish articles covering all areas of Surgery.
The journal aims to promote latest information and provide a forum for doctors, researchers, physicians, and healthcare professionals to find most recent advances in the areas of Surgery. Annals of Surgery and Perioperative Care accepts research articles, reviews, mini reviews, case reports and rapid communication covering all aspects of Surgery.
Annals of Surgery and Perioperative Care strongly supports the scientific up gradation and fortification in related scientific research community by enhancing access to peer reviewed scientific literary works. Austin Publishing Group also brings universally peer reviewed journals under one roof thereby promoting knowledge sharing.
Promoting a Culture of Abandonment Teresa R. Wagner Tere.docxamrit47
Promoting a Culture of Abandonment
Teresa R. Wagner
Teresa Wagner is a legal analyst specializing in human rights and right-to-life issues at Family Research
Council, a Washington-based organization with the following mission statement: "The Family Research
Council champions marriage and family as the foundation of civilization, the seedbed of virtue, and the
wellspring of society. We shape public debate and formulate public policy that values human life and up-
holds the institutions of marriage and the family. Believing that God is the author of life, liberty, and the
family, we promote the Judeo-Christian worldview as the basis for a just, free, and stable society.”
1 The death toll in Oregon will really begin to rise now. Attorney General Janet Reno has
decided that a federal law regulating drug usage (the Controlled Substances Act) somehow does
not apply to the use of lethal drugs in Oregon, the only state in the country to legalize assisted
suicide. The evidence will begin pouring in on how deadly assisted suicide can be, not just for
the individuals subject to it, of course, but for the culture that countenances it.
2 There are frightening and compelling policy reasons to oppose assisted suicide. Foremost is the
risk of abuse. Proponents of assisted suicide always insist that the practice will be carefully
limited: It will be available, they claim, only for those who request it and only for those who
are dying anyway (the terminally ill).
3 Such limitations are virtually impossible. People will inevitably be killed without knowing or
consenting to it. Several state courts have already ruled as a matter of state constitution^ law
that any rights given to competent patients (those who can request death) must also be given to
incompetent ones (those who cannot). Third parties make treatment decisions for this latter
group. Now legal, assisted suicide will be just another treatment option for surrogate decision
makers to select, even if the patient has made no indication of wanting to die.
4 What's more, the cost crunch in medicine virtually guarantees that hospitals and doctors will
eventually pressure, a" then coerce, patients to avail themselves of this easy and cheap =-
tentative,
5 Similarly, the confinement of this right to the terminally ill is impossible. As many groups
opposing assisted suicide have noted, the term itself is hardly clear The Oregon law defines
terminal disease as that which will produce death within six months. Is that with or without
medical treatment? Many individuals will die in much less than six months without very
simple medical treatment (insulin injections, for example).They could be deemed terminal
under this law and qualify for this new right to death.
6 More importantly the rationale for providing this new right almost demands its extension
beyond limits. After all, if we are trying to relieve pain and suffering, the non-terminal patient,
who faces years of discomf ...
Experts by Experience 2016: A compilation of patient storiesInspire
In cooperation with Stanford Medicine, Inspire presents the special report, "Experts by Experience 2016: A compilation of patient stories," the fourth in an ongoing series.
This document discusses how people with dementia and their families cope with bereavement and loss. It notes that grief can be a disenfranchised or ambiguous experience for those with dementia as they may forget losses or confuse past and present. Expressions of grief in dementia can include agitation, distress, or confusion about a missing person. It emphasizes the importance of person-centered care, reminiscence work, honesty and consistency when supporting those grieving with dementia.
Error is almost inevitable in our clinical practice so we should be prepared to help and prepare those individuals involved for the benefit of them, our systems and our patients.
Do you remember that patient you saw last night?': A phrase the strikes terror into the hearts of all physicians. The prospect of a patient coming to harm as a result of a mistake is terrifying but it can and does happen.
The consequences for the patient and their family are often tragic but what of the clinicians who made the error? For many the result of making a terrible error is life changing.
Those permanently harmed by error are often referred to as second victims with the consequences of terrible events being life-long.
This talk explores the predictable course for clinicians who are involved in error and asks whether we can prepare and support such individuals through a difficult time.
Cultural Competence in Palliative CareLinda Golley
The document discusses cultural considerations in palliative care, including goals, needs, and preferences of patients from different cultural backgrounds. It provides scenarios of palliative care patients with cultural issues related to decision making, family dynamics, religious beliefs, and expectations around independence. Keys to understanding a patient's cultural context include asking the patient directly, using knowledge of their world and life experiences, and paying attention to non-verbal cues and behaviors.
Ambiguous Loss Supporting families with missing loved onesMaureen Trask
Nov. 7, 2017 presentation to the Volunteers of Victim Services Wellington about Ambiguous Loss to support families with missing loved ones. Presented by Maureen Trask.
Donald Vincent Moncrief has worked for the United States Marine Corps, the San Diego Police Department, the Pugilistic Offensive Warrior Tactics, Eastlake Elementary School, and Rady Children’s Hospital.
Due in an effort to facilitate scholarly discourse, create yourronak56
The video discusses barriers to mental healthcare in communities of color. It profiles Toy Burton who started an organization called DeeDee's Cry after her sister died by suicide. The video highlights stigma, lack of representation in the mental healthcare field, socioeconomic barriers, and mistrust of doctors as barriers. It suggests increasing representation of people of color as therapists and addressing stereotypes to improve access.
The author discovered an opportunity to volunteer with the Global Medical Foundation in the Philippines through an American College of Surgeons website. This fulfilled a promise the author made 11 years earlier to return to the Philippines as a physician. Volunteering has given the author perspective on their own career and inspired gratitude for resources available in the United States. Performing surgeries in challenging conditions in other countries renews the author's passion for medicine. Volunteering has become an essential part of the author's medical career to find purpose and overcome challenges.
La health examiner erica ives - shapiro pr - march 2013Kelila Shapiro
The document discusses eating disorders and a therapist's new book on the topic. It notes that over 10 million Americans suffer from anorexia or bulimia, which are the two most common eating disorders. The therapist, Erica Ives, has suffered from and recovered from an eating disorder herself. Her book aims to educate readers on what eating disorders look like and how to help those suffering from them. Ives notes that eating disorders allow people to communicate feelings they can't express otherwise, and that expanding knowledge of the disorders can help identify early signs and support recovery.
The document discusses how perceptions of women's mental states negatively impact the diagnosis and treatment of heart disease. Both female patients and doctors are less likely to pursue aggressive treatment for heart symptoms in women. While heart disease presents differently in women, the medical field still follows a male-centered model. Changing these perceptions will require education about women's heart risks, creating unity among women's health advocates, and allowing more women to participate in medicine.
Mr. Thavamani was paralyzed from the waist down due to demyelinating polyneuropathy. He was depressed and in severe pain, and had lost hope for his future. Through regular visits from a medical team, physiotherapy, counseling, assistive devices, and community support, his confidence increased. He learned to stand independently with support and is working towards walking again and returning to his daily life activities.
In Conversation with Compassion and Care
Concern to ensure compassion and empathy are core experiences in care services are now a priority following appalling scandals in care homes and hospital settings. Of course, at a time of economic austerity and threats to health and social services, caring about those in socially excluded groups seems to be less of a priority for governments, national and local. Improving the health and wellbeing of the population at large is one approach to this that is creating a more compassionate and caring society, within which all citizens can expect fair treatment and supportive concern when they face hard times.
However, these aspirations then beg the question, why do we not have compassionate care in care services, and why is society no longer, or no more compassionate. This series of short essays from experts is refreshing and thought provoking. There is depth in the experiences that are shared, some intimate some heartbreaking. careif is planning to provoke more conversations in compassion and care, so please share with others and send your views/essays to enquiries@careif.org
http://www.careif.org/knowledge/commentary-and-analysis.html
The document discusses coping with loss and grief, explaining that understanding the grieving process helps manage feelings in a healthy way. It describes the stages of grief, including denial, anger, bargaining, depression, and acceptance. Finally, it emphasizes that support from others and the community is important for coping with loss, death, and traumatic events.
The document discusses physician burnout and argues that organizing toward collective action can help address burnout caused by feelings of powerlessness when treating patients facing socioeconomic hardships. It notes that while burnout is usually attributed to work overload and bureaucracy, its origins may also lie in caring for marginalized patients whose health issues stem from deep-rooted social problems beyond a physician's control. Organizing with others around such issues can combat isolation and empower physicians to enact meaningful change, providing a strategic and therapeutic approach to fighting burnout.
The document provides an agenda and background information for a workshop on metastatic colorectal cancer (mCRC) patient journeys. The workshop aims to illuminate the patient experience, explore barriers to third and fourth line treatment, identify solutions to barriers, and generate support/adherence ideas. The methodology section outlines that the workshop will involve gathering existing knowledge, discussions with medical professionals, sharing early insights and a draft journey map, conversations with patients and caregivers, input from a behavioral psychologist, and an insights presentation and innovation session. Key overarching insights from patient interviews include that mCRC changes people, it's difficult to talk about colon/rectal issues, patients feel a loss of power, and patients maintain hope despite their situation
1) Charlie, a respected orthopedist and mentor of the author, was diagnosed with pancreatic cancer but refused all treatment and focused on spending time with family, eventually dying at home.
2) Doctors experience death differently than most - they are aware of medical limitations and options and generally have a serene acceptance when facing their own mortality, opting for minimal treatment and dying peacefully.
3) The author argues that the medical system encourages excessive treatment out of fear of litigation and desire to avoid blame, even when treatment provides only misery, and that doctors still refuse such treatment for themselves by focusing on dignity and quality of life over aggressive measures near the end.
Annals of Surgery and Perioperative Care is an open access, peer reviewed, scholarly journal dedicated to publish articles covering all areas of Surgery.
The journal aims to promote latest information and provide a forum for doctors, researchers, physicians, and healthcare professionals to find most recent advances in the areas of Surgery. Annals of Surgery and Perioperative Care accepts research articles, reviews, mini reviews, case reports and rapid communication covering all aspects of Surgery.
Annals of Surgery and Perioperative Care strongly supports the scientific up gradation and fortification in related scientific research community by enhancing access to peer reviewed scientific literary works. Austin Publishing Group also brings universally peer reviewed journals under one roof thereby promoting knowledge sharing.
Promoting a Culture of Abandonment Teresa R. Wagner Tere.docxamrit47
Promoting a Culture of Abandonment
Teresa R. Wagner
Teresa Wagner is a legal analyst specializing in human rights and right-to-life issues at Family Research
Council, a Washington-based organization with the following mission statement: "The Family Research
Council champions marriage and family as the foundation of civilization, the seedbed of virtue, and the
wellspring of society. We shape public debate and formulate public policy that values human life and up-
holds the institutions of marriage and the family. Believing that God is the author of life, liberty, and the
family, we promote the Judeo-Christian worldview as the basis for a just, free, and stable society.”
1 The death toll in Oregon will really begin to rise now. Attorney General Janet Reno has
decided that a federal law regulating drug usage (the Controlled Substances Act) somehow does
not apply to the use of lethal drugs in Oregon, the only state in the country to legalize assisted
suicide. The evidence will begin pouring in on how deadly assisted suicide can be, not just for
the individuals subject to it, of course, but for the culture that countenances it.
2 There are frightening and compelling policy reasons to oppose assisted suicide. Foremost is the
risk of abuse. Proponents of assisted suicide always insist that the practice will be carefully
limited: It will be available, they claim, only for those who request it and only for those who
are dying anyway (the terminally ill).
3 Such limitations are virtually impossible. People will inevitably be killed without knowing or
consenting to it. Several state courts have already ruled as a matter of state constitution^ law
that any rights given to competent patients (those who can request death) must also be given to
incompetent ones (those who cannot). Third parties make treatment decisions for this latter
group. Now legal, assisted suicide will be just another treatment option for surrogate decision
makers to select, even if the patient has made no indication of wanting to die.
4 What's more, the cost crunch in medicine virtually guarantees that hospitals and doctors will
eventually pressure, a" then coerce, patients to avail themselves of this easy and cheap =-
tentative,
5 Similarly, the confinement of this right to the terminally ill is impossible. As many groups
opposing assisted suicide have noted, the term itself is hardly clear The Oregon law defines
terminal disease as that which will produce death within six months. Is that with or without
medical treatment? Many individuals will die in much less than six months without very
simple medical treatment (insulin injections, for example).They could be deemed terminal
under this law and qualify for this new right to death.
6 More importantly the rationale for providing this new right almost demands its extension
beyond limits. After all, if we are trying to relieve pain and suffering, the non-terminal patient,
who faces years of discomf ...
Experts by Experience 2016: A compilation of patient storiesInspire
In cooperation with Stanford Medicine, Inspire presents the special report, "Experts by Experience 2016: A compilation of patient stories," the fourth in an ongoing series.
Health & wealth agenda of the provincial federation of ABCsArnulfo Laniba
This document outlines the agenda of the Provincial Federation of ABCs to combat poor health and wealth issues. It discusses the current dismal state of disease, death, poverty, and bankruptcy, and identifies the medical-pharmaceutical system as failing and as the number one cause of death in America. Alternative approaches focusing on preventive medicine using natural remedies are presented. The wellness industry and networking are proposed as the main strategies to tackle these problems.
Experts by Experience 2015: A compilation of patients’ storiesInspire
In cooperation with Stanford Medicine, Inspire presents "Experts by Experience 2015: A compilation of patients’ stories." The special report is the third in an ongoing series.
Healing Hope How To Tell Your Children When Mommy Has Cancerbkling
When award-winning author Wendy S. Harpham, MD (When a Parent has Cancer: A Guide to Caring for Your Children) was diagnosed with cancer, her three children were 1, 3, and 5 years old. Over subsequent years, she guided them through her recurrences. In this webinar, Dr. Harpham shares insights about helping children through a mother's cancer diagnosis in healthy, hopeful ways. This webinar took place on December 17, 2018.
This document discusses common misconceptions about mental illness and provides facts to counter them. It begins by defining mental health and mental illness according to the WHO. It then lists several common misconceptions such as the ideas that mental illnesses are caused by supernatural forces, that only certain types of people experience them, or that seeking help makes the conditions worse. Each misconception is followed by a concise fact-based response explaining the real causes and nature of mental illnesses. The document aims to promote understanding and combat stigma by accurately informing about these conditions.
This document discusses issues with the US healthcare system, including high costs, lack of access to care, and medical errors. It notes that the US spends significantly more on healthcare than other developed nations, but does not achieve better health outcomes. Reasons proposed for the high costs include a shortage of doctors, expensive medical education discouraging new doctors, and inefficiencies in the system. The document advocates for reforms to improve patient safety, access to care, and reduce costs.
1) The document discusses the fear of ill health, which stems from physical and social heredity and is associated with the fears of old age and death. This fear is exacerbated by those who profit from selling health-related products.
2) Approximately 75% of people who visit doctors have hypochondria or imaginary illnesses brought on by the fear of disease itself. Suggestion can induce physical symptoms of feared diseases.
3) During a flu epidemic, the mayor of New York asked newspapers not to publish scare headlines about it, which successfully checked the epidemic within a month by reducing fear. Experiments have shown people can be made ill through negative suggestion alone. The fear of ill health has many psychological and physical
The document discusses the ethical dilemma of whether a physician should disclose all relevant medical information to a patient or withhold information at the request of the patient's family. It notes that informed consent requires full disclosure of a diagnosis, treatment options and risks. Withholding information violates patient autonomy and the ethical principles of veracity, informed consent and accountability. Full disclosure benefits the patient-physician relationship, allows patients to make their own decisions and provides hope, closure and palliative care options. It also benefits family cooperation and the patient's psychological well-being.
Intentional Health Detoxify, Nourish, and Rejuvenate Your Body into BalanceLucky Gods
Detox, Nourish, Bloom: Cultivate Intentional Health and Reclaim Your Radiant Self
Imagine waking up every morning feeling vibrant, energized, and in tune with your body's wisdom. ✨ That's the power of Intentional Health, your guide to ditching the diet doldrums and cultivating a holistic approach to well-being that nourishes from the inside out.
This book is your passport to a healthier, happier you, packed with practical tips and inspiration to:
Detoxify and declutter: Flush out toxins that weigh you down, both physical and emotional.
Nourish with intention: Discover the power of eating for vibrancy, not restriction.
Move your body with joy: Find exercise that fuels your spirit, not just your step count. ♀️
Rest and recharge: Prioritize sleep, relaxation, and self-care for inner balance. ♀️
Connect with your intuition: Listen to your body's whispers and tap into your innate wisdom.
Intentional Health is more than just a book; it's a transformative journey to:
Holistic Wellness: Embrace a 360-degree approach to health that encompasses body, mind, and spirit. 🫀🫁
Vibrant Living: Cultivate energy, joy, and a zest for life that radiates from within. ✨
Empowered Choices: Ditch diet dogma and make conscious decisions that nourish your unique needs.
Sustainable Habits: Build a foundation of healthy practices that last a lifetime, not just a fad. ️♀️
Your Best Self: Uncover your full potential and step into the healthiest, happiest version of you.
Ready to blossom into your healthiest, happiest self? Dive into Intentional Health and start blooming from the inside out today!
A mock opinion piece on the Singularity and the future of healthcare for the Trillion Dollar Challenges class. Explores the relationship between health technology and human interaction.
This document outlines best practices for breaking bad news to patients based on several models, including SPIKES, ABCDE, and BREAK. It discusses preparing for the conversation, building rapport, exploring the patient's understanding, announcing the diagnosis, addressing emotions, and documenting the discussion. The goal is to disclose information compassionately while supporting the patient and addressing their needs.
This document discusses changing the conversation around mental illness. It notes that Demi Lovato discusses her own diagnosis to remind people to seek help. It urges using respectful language when discussing mental health and not labeling people by their conditions. Stigmatizing words can discourage people from getting help. The movement aims to improve understanding and end discrimination against those with mental illnesses.
Pfizer vice president blows the whistlekirti betai
1) Dr. Peter Rost, a former Pfizer vice president and pharmaceutical industry whistleblower, reveals the close ties between the pharmaceutical industry and medical community.
2) Editors of two major medical journals, the New England Journal of Medicine and the Lancet, state that much of the current published medical research is unreliable due to conflicts of interest and biased studies.
3) A 2005 study found that most published medical research findings are false, calling into question the science used to develop medicines.
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"Toscha Seidel made a nation fall in love with the violin" -- Article from The American Scholar by Adam Baer about the storied violinist who was also a soloist in early Hollywood and a member of the first studio orchestras. He played his Stradivarius (now, the "da Vinci, ex-Seidel") for films such as Intermezzo, The Wizard of Oz, and Melody for Three, among other movies. He was friends and a collaborator with many of the Jewish emigré composers and musicians who arrived in Los Angeles after fleeing Nazism. He taught Albert Einstein, played with Charlie Chaplin, and was one of the violinist subjects in a song by George Gershwin. Copyright, Adam Baer, 2018.
https://theamericanscholar.org/the-sound-of-tinseltown/
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From Toronto With Love - The Atlantic - by Adam BaerAdam Baer
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The Pressure to Say You're OK -- by Adam Baer, Los Angeles Times
1. 6/1/2016 The pressure to say you're OK - LA Times
http://www.latimes.com/opinion/op-ed/la-oe-1209-baer-sickness-upbeat-notes-20151209-story.html 1/3
A
Opinion / OpEd
Op-Ed The pressure to say you're OK
By Adam Baer
DECEMBER 9, 2015, 5:00 AM
colleague recently announced that he'd been diagnosed with a life-threatening cancer. Don't
worry, he wrote. He promised to fight. He promised to recover.
As a survivor of multiple cancers and rare diseases, I've had to write my fair share of group
emails alerting friends and family to medical news. So I understand the impulse to sound upbeat.
Diagnosis emails and social-media posts are now a genre with set tropes and expected turns of phrase.
Los Angeles Times
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2. 6/1/2016 The pressure to say you're OK - LA Times
http://www.latimes.com/opinion/op-ed/la-oe-1209-baer-sickness-upbeat-notes-20151209-story.html 2/3
We swear we'll morph into rays of light during the darkest times in our lives. We vow to battle our
infirmities — as if that were possible beyond seeking treatment — and to become “well again.”
We do this because we want to shelter ourselves from fear as much as we want to bolster the spirits of our
loved ones. We may also feel the need to run damage control and manage ourselves like brands, lest we
alienate fair-weather friends or fail to reduce the professional harm that reports of serious illness may
bring.
When I graduated from college, my parents told me never to disclose my cancer history to colleagues or
employers. They understood on an intuitive level what a recent article in the journal Cancer confirmed:
Two years after a diagnosis, cancer survivors earn 40% less. By year five, they still haven't made it back to
their original salaries.
Despite these statistics, and despite the debatable power of positive thinking — I'm an optimist with a
taste for facts — I bridle at the social pressure to project exaggerated good cheer in the face of medical
uncertainty. If we deserve anything after a grim doctor's visit, it's the uncommon chance to be authentic
— even if that means remaining reticent, sobbing uncontrollably, attempting jokes that are mordant at
best, ignoring those who tell us how to feel, or asking for help and company. This is our chance to share
the disconcerting notion that we don't yet know how we'll go on — even if that means putting everyone
around us in mind of their mortality.
Promising to “recover,” besides, masks the reality that recovering from a medical problem today doesn't
mean what our outdated dictionaries say it does, what with mysterious late effects from treatments and
additional medical problems caused by the first ones.
“There's no need to insist that "everything will
return to normal." ... Chronic illness is
normal.