Service improvement in healthcare services-Uk

Service improvement in healthcare services-Uk

This module enables students to meet the following learning outcomes:
1) Critically analyse national health policy and the regulatory body’s guidance and how this influences your practice.
2) Critically examine how a particular aspect of service improvement has or would improve has or would improve the care of the patient.
3) Critically analyse risk assessment and how this relates to patient safety.
4) Critically analyse the NHS integrated governance agenda and how this relates to all of the above outcomes
5) Critically apply the principles of integrated governance to the development of professional or clinical practice
Critically analyse a specific aspect of your current or future practice which addresses the learning outcomes for this module:
Task:
Identify an opportunity for a Service Improvement Project from a recent practice placement experience, and discuss how this type of project contributes to the NHS Quality Improvement agenda. Evaluate how your identified project links to relevant English health legislation/policy for the area of practice, and consider any risks associated with such a project, for service users, practitioners and the delivery of nursing. You should refer to your own project to illustrate your discussions, via inclusion of a PDSA plan, measurement plan and any other relevant tools, in an appendix to this essay.

Defining Health In Pursuit Of Healthcare And Wellbeing

There are various concepts of health both lay and professional. Health is a complex subject and one that can be difficult to define, however The World Health Organisation, WHO (1984) cited in…. defines it as “The extent to which an individual or (group of individuals) is able, on one hand to realise aspirations and satisfy needs, and on the other hand to change or cope with the environment. Therefore seen as a resource for everyday life, not an object of living. It is a positive concept. Emphasising social and personal resources as well as physical capacity. This definition recognises that health is multi dimensional. (Lloyd, Hancock and Campbell, 2007)This piece of work will explore the concept of health and nursing, firstly describing the dimensions of health. It will then go onto give an overview of an adult individual including their health history. It will identify what determinants affect the individual’s health. The underpinning professional, legal and ethical principles of nursing that would apply in the event that the individual would require care will be explained. Finally the writer will identify how this piece of work has informed their personal concept of nursing. 192

DIMENSIONS

There are various aspects of health to consider when aiming to achieve overall good health and wellbeing, known as the dimensions of health. According to Ewles and Simmett (2004) there are six dimensions. Physical, intellectual, emotional, social, spiritual and environmental health also referred to as societal health. Physical health is concerned with the state of the body including its development, functions and maintenance. Good physical health can be achieved by eating a nutritious diet including drinking adequate amounts of water, participating in regular exercise and having regular health checkups. By doing so this will ensure the body is cleansed, energized, fit and that disease and illness is minimised. Intellectual health is being able to enhance knowledge and skills, make decisions, are creative, and have comprehension and common sense. Through interactions, being open minded, questioning and challenging things an individual is stimulating their mind therefore enhancing their cognitive ability and intellectual health. Emotional health which is sometimes referred to as psychological health is about acceptance of one’s own emotions, being able to cope and express them appropriately and recognise others feelings. It also takes into account the value they hold of themselves and their self esteem. Each individual has different ways of coping and enhancing their emotional health. Social health is having the ability to develop relationships with others including the wider community and maintain such relationships. It is also the ability to participate in society, have an active societal role and be socially accepted. One should be accepting and understanding of other cultures and the values and beliefs they hold. Spiritual health can vary in meaning for individuals. To many, spiritual health is considered to be about religious beliefs and about having faith, for others it is about the meaning of life and their own values and how they cope with certain aspects of their life. “Spiritual wellness combines a person’s ethics, values and morals. This component is what gives life meaning and purpose. It is based on faith, hope, love, optimism and forgiveness.”(Floyd, Mimms and Yelding, 2008) Environmental health can comprise of both internal and external. There are some aspects to individuals environmental health they have no control over but there are some in which they do; for instance their lifestyle. Everything that surrounds an individual can contribute to their health. Individuals usually cannot change their internal environment, their genetic blueprint and pre-dispositions. “Balancing of these components is necessary to achieve a high level of wellness” (Floyd, Mimms and Yeilding, 2008) Each dimension is of equal importance and each should be considered in order to view an individual’s health holistically. All overlap to an extent; they interact and influence one another. One imbalanced dimension can significantly impact on the others. These dimensions are also reflected In Maslow’s hierarchy of needs in order to reach self actualization, a person must move through the stages meeting fundamental needs, physiological, safety, love and belonging, esteem and the self actualization. 487

OVERVIEW OF INDIVIDUAL

For the purpose of this assignment the individual will be referred to as Mrs. X to maintain confidentiality. Consent has been obtained from the concerned individual.

Mrs. X is a 43 year old, single mother of three children who lives in a socially deprived area of north Lanarkshire. Mrs. X was raised in North Lanarkshire with mother, father, older brother and younger sister. Mrs. X is very intelligent and achieved well at school. When she left school she went on to become a psychiatric nurse. She worked at hardwood hospital and carstairs state hospital at this time Mrs. X earned a good living and was financially secure. In 1993 shortly after the birth of her second daughter, Mrs. X’s father to whom she was very close to died. Mrs. X never returned to work as a nurse after this time. She was a fulltime mother for a number of years, during this time she met her husband and had a son. She divorced after 4 years. When her youngest child started school she returned to work and now works in social work department as a carer on a relatively low income. Over time Mrs. X has suffered numerous health issues, when pregnant with her first child she suffered a deep vein thrombosis, it has recently been discovered she suffers a genetic blood disorder. She has trouble with her bowels however after many investigations a cause or diagnoses has yet to be identified. She has allergies, suffers back ache, and has early onset menopause and related symptoms. She is currently undergoing investigations into her liver function which is thought to be associated with her alcohol consumption. 275

DETERMINANTS OF HEALTH

Naidoo and Wills (2009) discuss the many factors that can contribute to an individual’s health. These factors are known as the determinants of health. According to WHO (n.d) these are “the social and economical environment, the physical environment and the individuals own characteristics and behaviours”. Much research is conducted into such determinants to identify causes and help establish ways of reducing health inequalities. Health promotion programmes are one way of trying to reduce inequalities though raising awareness of such factors. In relation to Mrs. X there are many determinants that affect her health. Statistics show the area in which she lives has one of the lowest life expectancies in Scotland especially amongst woman, it also has a high number of drug and alcohol misuse, single parent household, cases of individuals with mental illness, and poverty. All of which are evident in Mrs. X situation suggesting her health are compromised by living in this area. Although Mrs. X is employed she is not financially secure and does not have disposable income. This affects her self esteem and the value she holds of herself. Her financial situation prevents her from participating in many things, therefore impacting on her social and emotional health. Her occupation involves manual handling, which with her existing back trouble can impact on her physical health. Being single impacts on Mrs. X, she lacks interaction with other adults, preferring her on company. Being alone leads to her consumption of alcohol. Mrs X knowledge and education also influences her health, having previously been a nurse she is well away of the impact certain things have on her health, however does not use this to her advantage, she tries to avoid going to her GP and usually self diagnoses which means she is depriving herself of what could be necessary treatments. Mrs X has an unhealthy relationship with alcohol although she does not think she has a problem. She consumes alcohol most days. This aspect of her lifestyle is impacting greatly on her health. Her diet is poor as she replaces food with alcohol, she has substantial problems with her liver, and she is deficient in most essential vitamins and mineral. Her emotional and social health is also being affected, she has low self esteem, suffers depressive moods, she withdraws and isolates herself. Her cognitive ability will start to suffer with the continuous consumption of alcohol.mrs x is overweight; this is likely due to her diet, alcohol consumption and lack of exercise. This affects her self esteem. Many of Mrs. X physical health troubles are genetic. She suffers from hypertension as does her mother and sister, she also has a hereditary hypercoagulability disorder. She also has pre-dispositions to other illnesses. Heart disease and cancer are common in the immediate family as are diabetes mellitus and glaucoma. Many of the medications that Mrs. X takes have contributory effects that add to the state of Mrs. X overall health. Many of the determinants that evidently contribute to her health are within her control, given the appropriate support and advice of healthcare professionals Mrs. X can take steps to improve her health. 518

PROFESSIONAL, LEGAL AND ETHICAL PRINCIPLES

In the event that Mrs. X would require nursing care there are many professional, legal and ethical principles that would apply to her care.

“The law and ethics is the framework in which professional issues are discussed and measured”. (reeves and orford, 2003). Therefore all three combine together in most situations in practice. The Nursing and Midwifery Council (NMC) are the regulators for nurses and midwifes. The NMC is in place to safeguard the health and wellbeing of the public by setting standards that must be followed,” the code of professional conduct, performance and ethics” (nmc, 2004) Individuals being cared for must be able to trust those delivering their care therefore nurses must act with integrity. Nurses must treat each person as an individual and respect them, be non-judgemental and not discriminate. They must demonstrate consideration when delivering care and respect ones privacy and dignity. People have the right to confidentiality. Information should only be shared with necessary people in the interest and safety of the person being cared for. This is a legal aspect; confidential information is protected under the data protection act 1998. Nurses should act as an advocate for those in their care to help them receive appropriate treatment, support and information. When acting as an advocate a nurse should be aware of legislation regarding mental capacity such as Adult with Incapacity (Scotland) Act 2000 to ensure those who lack capacity are safeguarded. Nurses should involve people in their own care as far as reasonably possible to promote their independence. Another principle that’s not only a professional principle but also a legal requirement is consent. Nurses must gain consent before carrying out any procedure of care. They must respect that person’s choice and be able to justify their actions in the event they had to provide care in an emergency. Professionals must work effectively together in a multi disciplinary team to ensure the best possible care is being provided. Nurses must be aware of professional bounderies and not conduct themselves in such a way as to compromise their professional relationships. Nurses have a professional and legal duty of care, they are accountable for their own actions and they must uphold the reputation of the nursing profession. A nurse must take reasonable care to avoid causing harm or injury to any person through negligence. They must also demonstrate competence and should keep their knowledge and skills up to date. Recordkeeping is a profession principle but it is also a legal requirement. It is the nurse’s responsibility to ensure records of care and assessments they have made are up to date, accurate and clear. They should be kept secure and should not be altered or tampered with. Recordkeeping is evidence that a nurse is fulfilling their professional duty. Nurses have a legal responsibility to report and record accidents and incidents. There are many legal boundaries that apply to healthcare situations. It is therefore important that nurses are aware of legal principles (kenworthy, snowley and gilling, 2006). Legislation is a fundamental part of healthcare with many acts in place to protect both the professional and the person being cared for. All professionals should be familiar with current legislation relevant to their practice. The law can be divided into two, criminal law and civil law. “The majority of healthcare situations that need legal involvement will be civil matters”.(kenworthy, snowley and gilling, 2006). Ethics and morals play a huge role in nursing practice. Downie and calman(1994) cited in Brooker and Waugh (2007) argue that all clinical and professional decisions have a moral aspect to them. Nurses have to make decisions when faced with dilemmas with the intensions of doing good for the person being cared for and avoid causing them harm. They have to decide whether they ought to carry out certain actions, if they have a duty to do such things. There are two main ethical theories deontology which is concerned with ones motives for action, their duties and responsibilities. Utilitarianism is to do with the consequences of actions, what the outcome would be. A nurse should have knowledge and awareness of not only the professional morals and ethical values but their own as well. Brooker and Waugh(2007) discuss the main principles of ethical practice, that nurses have to respect individual’s rights to autonomy, the right to make their own decisions and choice however this can be overruled in the interest of others of if one is unable to make decisions clearly. Individuals have a right to justice, they have protection under law, and they should have a choice as to what course of action they wish to pursue to obtain justice. Nurses should be aware of their accountability. Another principle that should be applied in care is non- malefience which means to do no harm. This is part of a nuses duty as stated by the NMC. They should carry out care in the best interests of the individual known as beneficence and be able to justify that care. Nurses must be truthful, referred to as veracity this is essential in building meaningful trusting relationships with others, not only those in their care but also their relatives, other colleagues and professionals this is important to deliver the best possible care. 870

MY CONCEPT

Since researching the different aspects of nursing and writing this assignment my concept of nursing has definitely changed. I feel I held many of the lay concepts of health however now I feel I am beginning to look at health from a professional perspective. I am more aware of the factors that contribute to people’s health and how many of these can be influenced. Gaining an understanding of how these factors affect the dimensions of one’s health and having gained an awareness of how these dimensions interact and impact on one other I can see why taking a holistic approach in assessing individuals is a positive aspect and one that is promoted. It has also enhanced my knowledge of the principles that are applied to the nursing profession, the professional principles, guided by the NMC’s code of conduct, the legal principles, relevant legislation and the ethical principles that should be applied in decision making in clinical practice. Overall I have been informed of the concept of health as viewed from the nursing profession which I feel will benefit me immensely as I continue the programme of study and practice with outcome of having a career in nursing. 197

CONCLUSION

This assignment has concluded that there are various dimensions to one’s health that can be affected, therefore taking a holistic approach in assessing an individual aims to ensure all these dimensions are addressed. It has identified the many factors that can influence and determine ones health although these vary for each individual. The assignment has discussed which determinants can be influenced to improve health and wellbeing. The underpinning professional, legal and ethical principles that apply in the delivery of care have been explained. The writer has also mentioned how writing this assignment has informed their concept of nursing. Overall it has been identified that there are many aspects to consider when providing care to achieve a standard of excellence. 120

discuss a situation where you noticed, interpreted, and responded, and then reflect upon the situation based on its context and your background in nursing, and how both contributed to the clinical judgment that you made.

discuss a situation where you noticed, interpreted, and responded, and then reflect upon the situation based on its context and your background in nursing, and how both contributed to the clinical judgment that you made.

 

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Question description
QUESTION ONE
Reflection is a process used in nursing practice and involves noticing, interpreting, and responding (Tanner, 2006, p. 208). Discuss strategies you could use to share this process with others in your area of nursing practice using Tanner’s model as a guide. For example, discuss a situation where you noticed, interpreted, and responded, and then reflect upon the situation based on its context and your background in nursing, and how both contributed to the clinical judgment that you made.
Support your discussion and opinions with facts, relevant examples from personal nursing practice, and at least two citations from the reading or peer-reviewed professional nursing literature.
See the Nursing Syllabus Standards & Policies Document for Discussion Participation Guidelines & Grading Criteria.
Remember to use APA 6th edition formatting for all discussion posts and reference citations.
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A male client complains of sporadic epigastric pain, yellow skin, nausea, vomiting, weight loss,

A male client complains of sporadic epigastric pain, yellow skin, nausea, vomiting, weight loss,

A male client complains of sporadic epigastric pain, yellow skin, nausea, vomiting, weight loss, and fatigue. Suspecting gallbladder disease, the physician orders a diagnostic workup, which reveals gallbladder cancer. Which nursing diagnosis may be appropriate for this client?
A male client complains of sporadic epigastric pain, yellow skin, nausea, vomiting, weight loss, and fatigue. Suspecting gallbladder disease, the physician orders a diagnostic workup, which reveals gallbladder cancer. Which nursing diagnosis may be appropriate for this client?

A. Anticipatory grieving
B. Impaired swallowing
C. Disturbed body image
D. Chronic low self-esteem

Essay On The Treatment of Parkinsons Disease

Parkinson’s disease is a neurological condition that affects the sufferer’s mobility and speech. It affects the central nervous system, leading to a person’s inability to control muscles throughout the body. It is a disease whose treatment does not intend to cure it but instead, aims at controlling its manifestation. There are various ways in which this can be done. It may involve the use of drugs or the performance of surgery. Doctors strongly recommend exercise to try to keep muscles strong. It progresses gradually or severely from the early stages with mild symptoms to later stages with severe symptoms.

The disease is a result of lowered formation and action of dopamine which is produced by the dopaminergic neurons found in the brain. This knowledge led to the formation of drugs that will either increase the formation or mimic the actions taken by dopamine in the brain. This was important because an increase in the levels of dopamine would lead to a reduction of the effects of the disease. All the drugs used to control the disease include dopamine as their main active agent regardless of how it works. Depending on which class of drugs it belongs to, it may either mimic or produce dopamine.

Among the earliest forms of treatments are the anticholinergics. These were used even before the introduction of Levodopa, which is now the most widely used drug. The anticholinergics had very little benefits when compared to the harmful side effects caused by usage. The side effects include having a dry mouth, urine retention (which especially occurs among men), and very severe constipation and nausea. There are some other side effects that occur that are more serious and are among the major reasons why the use of these drugs has become minimal. These include confusion, memory loss, and hallucination (http://www.mayoclinic.com).

The realization that the benefits seen were much less than the side effects it causes has led to the reduction of its prescription. Since some anti-depressants and antihistamine’s tend to have almost the same effect as the anticholinergics, doctors will prescribe them to older people who are suffering from this terrible disease. Once an individual experiences any of the serious severe symptoms, it is advised that the use of the drug be stopped immediately.

Levodopa is a drug that was introduced in 1967 and is currently the most commonly used drug. It is most commonly referred to as Sinemet and is used to help restore ones control over ones muscles. Levodopa is referred to as the gold standard of Parkinson’s treatment because it is usually used as the first line of defense. The reason a sufferer of Parkinson’s can’t just take Dopamine itself is because Dopamine cannot breakthrough the blood-brain barrier. Levodopa can get through this barrier and is converted to Dopamine once it reaches the brain. It therefore increases the level of Dopamine and counters the effects of the disease. The conversion to Dopamine is what leads to the positive effects that a patient experiences when using the drug (Henkel).

Levodopa however has very serious side effects which include nausea and dyskinesias (involuntary movement). This occurs because only a small percentage of the drug actually reaches the brain to be transformed into Dopamine. The rest of it is transformed into dopamine in the body. It therefore becomes necessary to use Carbidopa, which delays the metabolism of Levodopa until it reaches the dopaminergic neurons in the brain. The combination helps reduce the side effects caused by the drug. Carbidopa delays the metabolism of Levodopa, keeping it from metabolizing in the body. This helps to greatly reduce the side effects felt by the user.

The other problem posed by the use of this drug is that its dosage needs to be increased over time. It has also been observed to work on and off without any explanation or reason. This makes it unreliable because its effects are not constant, and at times the patient gets violent attacks while still under medication. The various side effects and unreliability of levodopa leads to the necessity to combine it with various other drugs to make it more effective. Some of these drugs can be used on their own while others actually require to be used with the Levodopa-Carbidopa combination.

A cluster of drugs called Dopamine agonists are usually used in a combination with the Levodopa-Carbidopa drugs. They can however also be used on their own if the disease has not greatly progressed. Also, it is recommended that these drugs only be used alone in young adults. This class of drugs does not produce or help in the production of dopamine but instead imitates the effects that Dopamine has in the body. They tend to act on behalf of Dopamine (http://www.mayoclinic.com).

This class of drugs include; Apokyn, Requip, Parlodel and Mirapex. Parlodel has been used very little of late. This is because it had very serious side effects that endangered the patient more than it benefited him/her. It would cause inflammation in the lungs and/or heart valves of the user and would lead to further deterioration of the patient’s health. In general this class of drugs has side effects that are almost similar to those of carbidopa-levodopa but with slight differences. The effects of having involuntary movement are reduced while those of hallucinations and/or sleepiness are increased.

The drug Mirapex takes up the role of dopamine in the body as it is one of the dopamine agonists. When it is used in the absence of Levodopa-Carbidopa, it causes a 30% improvement in the health of the patient. When used in combination, it is able to reduce the intake of the Levodopa dosage by about 25%. Requip is also a dopamine agonist that can also be used either alone or with Levodopa. When used together with Levodopa, it can reduce the intake of Levodopa by around 31%. The reduction of Levodopa dosage decreases side-effects to the patient (Henkel).

Catechol-o-methyltransferace inhibitors, which are usually abbreviated as COMT inhibitors, are used to block the enzymes that break down the Levodopa into Dopamine before it reaches the brain. They can be used in combination with the Carbidopa-Levodopa therapy. The two main COMT inhibitors are Tasmar and Entacapone. Tasmar is rarely used because of its severe impact on the health of the user. It causes severe liver damage and hence is only used as a last resort if the patient has failed to respond to any other therapy (http://www.mayoclinic.com).

Entacapone does not have side-effects as severe as those of Tasmar and is therefore recommended over Tasmar. Its major side-effect is the involuntary movements experienced by the user. It works in conjunction with the Carbidopa-Levodopa therapy by increasing their availability. This is done by blocking the enzymes that break down the substance into Dopamine until the drug is already in the brain. This then means that the effects of Levodopa-Carbidopa are prolonged because they occur only in the brain. Stalevo, another drug, is the result of a combination of Carbidopa, Levodopa and Entacapone.

Selegiline, also referred to as Eldepryl, is another drug that can either be used with or without the presence of Carbidopa-Levodopa therapy. It works by preventing the metabolism of Dopamine. It does this by slowing down the activity of one of the enzymes that metabolize Dopamine. This is the monoamine oxidase B which is abbreviated as MAO-B. The use of Selegiline has other positive effects like delaying the need of Carbidopa-Levodopa. When combined with Carbidopa-Levodopa it improves the effectiveness of the drug. It can however have some adverse toxic reactions when combined with Demerol which is a narcotic drug.

Apart from ingesting drugs, they can be administered through the skin through the use of a silicon-based patch. Rotigotine is a dopamine agonist drug that can be administered through the skin, but can only be used in the early stages of the disease. This is called Neupro-rotigotine transdermal system. The patch has to be changed every 24 hours. It works by stimulating the Dopamine receptors in the body. Its side-effects include skin reaction where the patch is, hallucinations, insomnia, drowsiness, sleep-attacks, nausea, vomiting and the most severe is the reduction in blood pressure once the person stands up (http://www.fda.gov).

Amantadine is another drug that is used in treatment of Parkinson’s disease but its use was discovered by accident. Initially it was created to be an antiviral used in the treatment of influenza and was approved as such in 1976 by the Food and Drug Administration. It was however discovered to provide short term relief when used alone in the early stages of the Parkinson’s disease. When it is combined with Carbidopa-Levodopa it can be used by those in the later stages. It has side effects that mostly involve swelling of the ankles and turning skin color purple (http://www.mayoclinic.com).

In every human beings body, there is the presence of coenzyme Q10 which is produced by the mitochondria. This enzyme is used in the transport of electrons so that they can gain energy from the oxygen inhaled. This is done in the process called cellular respiration. The levels of this enzyme are very low in those suffering from Parkinson’s disease. These people can therefore benefit greatly by having more of this enzyme. This can only be achieved by taking supplements which can be bought from a pharmacy. This aids in helping to slow down the onset of the disease.

Apart from the use of drugs, there are various surgeries that can be used to control the effects of the disease. One of the surgeries is pallidotomy which involves the destruction of a small bit of the globus pallidus. Doctors believe all people who are suffering from Parkinson’s have an overactive globus pallidus. The procedure is done by drilling a small hole in the skull and using an electric probe to kill part of the pallidus. It can only be done when the patient is sedated but awake so the doctor can judge the patients reactions to stimuli. There is a globus pallidus on each side of the brain, but the operation can only be done on one side at a time. Its side effects mostly involve impaired speech (http://www.fda.gov).

Thalamotomy is another surgical procedure used in the control of Parkinson’s disease. It is only performed on those patients who are experiencing tremors in either the hands or the arms that become too severe to handle. Usually the tremors are so bad they disable the person. It involves the destruction of a specific group of cells that are located in the thalamus in the brain. The surgery reduces or completely eliminates the tremors in around 90% of those who undergo the procedure (http://www.fda.gov).

There is also the presence of a gadget that can be compared to the pacemaker used for cardio problems. It is known as the brain pacemaker (http://www.fda.gov).

This form of therapy is referred to as Active Tremor Control Therapy. It involves the surgical implantation of an insulated wire to the brain. It is placed in the thalamus region of the brain, the subthalamic nucleus, and also the globus pallidus area of the brain.

The whole system includes three components which are the: lead, extension and the neurostimulator. This system is referred to as Deep Brain Stimulation because it occurs directly inside the brain. A small hole is made in the skull and through it the lead is inserted into the brain. The lead is a very thin insulated wire. The tip of the lead is in contact with the area that has been targeted. Once it has been implanted, it is connected to the neurostimulator by the extension which is also an insulated wire (http://minds.nih.gov).

The extension passes under the skin and moves from the head, to the neck, the shoulder and finally to where the neurostimulator is located. The neurotransmitter is located either under the collarbone, in the abdomen or the lower chest area just directly under the skin. The neurotransmitter involves a battery pack that sends electrical impulses to the brain. This is done through the extension and the lead. When the person is undergoing tremors, he or she is supposed to pass a handheld magnet over the location of the neurostimulator.

The electrical impulses that are sent by the neurostimulator work by blocking the electrical signals that are the cause of the Parkinson’s disease symptoms. They are dysfunctional brain signals and they are the cause of the tremors. This procedure is preferred because it does not destroy the nerve cells and when one wants to stop its use it is as easy as having the system surgically removed.

Works Cited

  • “Deep Brain Stimulation for Parkinson’s Disease Information.” NINDS. 22 Nov. 2007 .
  • “Henkel, John. “Parkinson’s Disease: New Treatments Slow Onslaught of Symptoms.” FDA. 22 Nov. 2007 .
  • “Neupro Patch for Parkinson’s Approved.” FDA. 22 Nov. 2007 .
  • “Parkinson’s Disease: Treatment.” MayoClinic. 22 Nov. 2007

Identify the wellness of nursing diagnoses based family health assessment.

Identify the wellness of nursing diagnoses based family health assessment.

Select a family to complete a family health assessment. (The family cannot be your own.)Before interviewing the family, develop three open-ended, family-focused questions for each of the following health patterns:NOTE: Your list of questions must be submitted with your assignment as an attachment. After interviewing the family, compile the data and analyze the responses. In 1,000-1,250 words, summarize the findings for each functional health pattern for the family you have selected.Identify two or more wellness nursing diagnoses based on your family assessment. Wellness and family nursing diagnoses are different than standard nursing diagnoses. Prepare this assignment according to the guidelines found in the APA Style Guide, located in the Student Success Center. An abstract is not required. This assignment uses a rubric. Please review the rubric prior to beginning the assignment to become familiar with the expectations for successful completion.

Discharging Older People From Hospital To Care Homes

Discharging older people issue is the most important in today’s environment. Realising this, it is necessary to extract the fact in present situation of the older people. This study explored the experiences of older people being discharged from hospital to nursing and residential homes in the North East of England. While there has been considerable research which has looked at the discharge of patients from hospital to their own homes, little literature could be found which addressed discharge to care homes.

The discharge of older people to nursing and residential homes (care homes) represents a major life change for older people. Which has however received less attention in the nursing research and policy literature than discharge to the patient’s own home. These older people moving into nursing or residential care homes. However present a different set of responsibilities which may not be quite so obvious, or appear so pressing , yet which correspond with many of the definitions and model of nursing which emphasize the role of the nurse in supporting patients through process of loss and change.

Discharging planning research may focus on the primary secondary care interface, that is integration of hospital and community care services, care homes increasingly represent another sector the independent sector which is comprised of either private business or voluntary agencies. The National Health (NHS) and Community Care Act of 1990 (Department of Health 1990),where Social Services departments became responsible for developing and purchasing packages of care for older people, there has also been in increased requirement for health and Social services to work together.

This issues of collaboration and co operation are more complex than if the only interface involved is that between the hospital and community services. Interviews and written responses from members of staff in the hospital and in care homes, found that there was a lack of clarity over whose role it was to initiate such discussions.

This study explored the area of support for older people being discharged from hospital into a care home. The main aims of the study were to investigate the experiences of older people to identify possible forms of support that might be needed for available. The study was funded by a National Health Services Executive (Northern and Yorkshire Region) research programme which funded practice development studies in professions allied to medicine. The role of research team was not therefore to reflect and act upon a staff initiative, but to direct a study was suggested by a reading of the available literature research. The consequences of this position have been explored by some authors like Meyer 1993, and likely to impact upon processes of change in the way that the staff who are asked to develop their practice do not see themselves as having ownership of the research study.

The first chapter is about the experiences of the older people being discharged from hospital to discharge to nursing and residential homes in the North East of England. While there has been considerable research which has looked at the discharge of patients from hospital to their own homes, little literature could be found which addressed discharge to care homes. Similarly in other chapters describes about the reflect of an assumption that this form of discharge is less problematic, it is arguable that this is only the case for staff- there is a body of literature on re-location which suggests that the move to a care home is a major life event for older people. Taking a qualitative approach, this study interviewed 20 older people and 17 of their family members after discharge from hospital to a care home. We found that few people had been offered opportunities to discuss their move with nurses, and that older people tended to adopt a stoical attitude. In focus groups, interviews and written responses from 23 members of staff in the hospital and in care homes, we found that there was a clarity over whose role it was to initiate such discussions. The paper concludes with some discussion of the implication for nursing practice of changing care interfaces.

There is a body of research in the nursing literature which has looked at the discharge of older people from hospital. Discharge from the hospital has been an area of concern for nursing and health care practice for some time, with numerous research studies describing records of 32 older people who were to be discharged to the community following a hospital stay and found a lack of recorded information in all areas of the nursing process, from nursing assessment to care plan evaluation. This made the co-ordination of services to meet the needs of the older person difficult, and Waters concluded that neither doctors nor hospital nurses identified assessment planning for discharge home as a priority. Furthermore, a quarter of those older people interviewed did not recall having been asked about coping at home or being given any advice about his, even though all the sample had supposedly undergone some form of pre- discharge assessment. Waters also noted a lack of knowledge about medication by patients after discharge and identified the quality of information given to district nurses by the hospital as being problematic; for example, in some cases, problems identified in the nursing care plans as still being current at the time of discharge were not communicated to community nurses. Waters stressed the need for through assessment, accurate record-keeping and the availability of written information in order for successful discharge to take place, but also cautioned against generalising the results of her exploratory study. These findings, however, are supported by subsequent studies including King and Macmillan (1994), Jewell (1993), victor et al.(1993) and Tierney (1993).

A common theme throughout these studies is the issues of responsibility, in other words

among the various professions involved in the discharge process, in which one takes the lead in co- ordinating the process, or carrying out the different parts of it. Not only there is concern about formal allocations of responsibility, but also about informal negotiations different communication about the roles which different professionals take.

A number of recommendations have been made in the UK in response to these growing Professionals and public concerns. The department of Health (1998) recommendations, for example, stressed the need for discharge planning to commence as soon possible after admission; the importance of good communication networks between all parties involved in the process and the need for improvement of patient and relatives in decision making, ides that were also articulated in The Patient’s Charter (Department of Health 1992).

Moving into a care home

The literature in the discharge of older people from hospital, therefore , indicates that this area of practice is problematic, and that older people do not always receive the support that they need. There is also another body of literature which suggests that moving into a care home is an event or process which likely to increase the need for support, because of the stress involved, of disruption to lifestyles, of loss of home and of adopting to a new environment (Morgan et al. 1997).

For example, Nay (1995) has described both material and abstract losses attendant on moving into a care home. The loss of material possessions can include one’s home and personal belongings, while more abstract losses include loss of role , life style and freedom. Nay also highlighted the loss of home can mean much more than a change of living environment, as researchers have found, as older people have identified their home with feelings of autonomy and control and part of their identity (Golant 1984, Sixmith 1996, Willocks et al. 1987).

Moving into a new environment, such as a care home, is something which can carry be very stressful, both in anticipation and in realization (Reed and Rroskell Payton 1996, Reed et al.1997). Older people not only need to negotiate and to learn about a new physical environment, but also about the social world to the care home, the routines and behaviours of their fellow residents and to staff. For some, the prospect of such work can be daunting , and if apprehension is coupled with a sense of loss and dislocation from a previous lifestyles and personal identity, then being discharged from hospital into a care home represents a life event with, potentially a profound impact on older people , and one which requires some recognition and support from nurses. Moreover, previous studies by Johnson et al. (1994) and Retinas (1991) suggest that moving into a care homes is often accompanied or precipitated by major changes in health, social support and ability to cope.

A supportive role is advocated in much nursing literature where the nurse-patient relationship is discussed. Which some, like Armstrong (1983), might suggest that this relationship has been a recent ‘fabrication’ in nursing , the arguments for developing communication and interpersonal skills in nursing are difficult to refute. As smith (1992) has argued, ’emotional labour’ is an important part of nursing care if patients are to receive more than cursory processing through the health service system, and if they are to have some of their emotional and psychological needs addressed. Moving away from a restricted psychological and social aspects of health care is a move which is gaining around in many areas of nursing and health care, and which permits a more holistic view of the patient (Cooper et al. 1996). More specifically, Nolan et al. (1996) have argued that the nurse has an important role to play in the process of decision making when older people are considering moving into a care home, and that this role may involve advocacy to ensure that the interests of older people are addressed.

The literature, then, seems to indicate that the discharge of older people from hospital is something that is, by and large, poorly managed by nurses and other staff, with determined consequences for older people. The literature does not provide much information about the discharge of older people from hospital into care homes since much of it concentrates on discharge homes. We can, however, extrapolate from the literature that exists on the impact of relocation and loss of home on older people to argue that, while these administrative and organizational problems of ensuring that services are available which are attendant on a discharge home, that they present a different set of problems which are emotional and psychological. These problems may be primarily problems for the older people concerned, but there is also a strongly argument in the nursing literature to suggest that they should be the concern of nurses. The gap in the research literature therefore would seem to be in this area of support-what older people need and want, and how nurses can meet these needs.

The interviews with older people had a loosely structured interview agenda focusing on their experiences of discharge processes and any areas which they felt were problematic, or care that they found particularly helpful. This interview style was adopted in order to ensure that interviews were focused enough to allow respondents to introduce new topics areas. The discussion groups to develop guidelines adopted focus group techniques (Kitzinger 1995) to elicit opinions and ideas from the participants. Many focus group techniques assume that members have no previous contact with each other, and concentrate on eliciting spontaneous to questions and ideas. As members of the groups in this study were work colleagues, the interview format was designed to elicit general group perspectives in the context of professional roles and cultures (Reed and Payton 1997).

Patients recently discharged from the study hospital (part of a large acute care Trust in the North of England)to the independent sector within a 10-mile radius of New castle were identified from hospital records. They were visited by the researcher in the care home within 4 weeks of their discharge and invited to participate in the study. These patients and their significant others were interviewed to identify and describe their experiences of discharge. The interviews were conducted in the care home or in the respondent’s own home, and followed a semi-structured interview schedule which outlined the main areas of the study. Patients’ case notes were also examined for information about discharge arrangements and plans, and to provide background material.

In the analysis of the data, however, it was important to distinguish between the feeling of the older people about the loss of their home, process of moving, and their new life in the care home. Some people would be sad about the loss of their home but happy about the life in the care home. Others would be happy about leaving their home, but would not like the care home. It was clear that there were many different views which depended on personal perspectives and attitudes, and the circumstances precipitating hospital admission and discharge to a care home.

Among these individual stories, however, there was one theme which remained constant: the passivity of older people in the process of living. They did not expect support from staff, and their coping strategies centred mainly on stoicism. As one person told us:

Well, you just have to get on with it, I mean there’s no point in making a fuss.

Some older people expressed a concern to avoid being a burden to others, either staff or family members. These people ‘had better thing to do’ as one man put it, and for the staff is included looking after older people made comments that suggested that these ideas had also come from nursing staff- where they talked about nurses telling them that it was time to move on, or that they could not stay in the hospital for ever. For example one person argued that:

They (the staff) said that it was about time I was going, and they were right.

It was also striking that they did not think of themselves as people with any choices or control over care decisions- the older people in our study did not voice any objections to the verdicts of staff that they should move into a home, not did they seem to expect to exercise much choice over the home they moved to. The choice of home was delighted to family members or social workers, and could be made, given that they were too frail to visit home themselves. As one person told us:

My daughter sorted all that out- I could not go round those homes because I cannot get about. I had to rely on her.

It did not seem that any alternatives had been suggested, for example help in making a visit to the care home with transport and assistance.

The older people had also expected to have to fit in with care home regimes, and were surprised that the care home allowed them any choice or freedom. One lady, for example was surprised to be ‘allowed’ to order a newspaper- she had not expected to be able to do this. Their ideas about care homes had been vague and based on snippets of information gathered from friends, acquaintances and the media, rather than any clear information. As one person told us:

It was like taking a step in the dark. I did not know what to expect.

Care home staff confirmed this, saying that often older people seemed to have little idea about what life in a care home would be like.

Family perspectives

The ideas that they were not needy enough to be in hospital seemed to be shared by staff and older people. Family members, however, seemed less convinced by this thinking, and expressed more concerns about the process being rushed. These concerns stemmed from anxieties over the health of the relative, but also because of the process of choosing carefully. As one family members told us:

I had to go out and find a place, quickly because she was coming out. I went to see a couple, but I did not have a time to work through the list.

The ‘list’ that this person talked about was a list of homes registered with the Registration bodies of the Local Authority and Health Authority, and as such contain no information beyond addressed and numbers of beds. For most people in the study this was not enough information- they had very little guidance on what to look for in a home, or how to evaluate the care given. At the same time, family members felt a huge sense of responsibility for making the ‘right’ decision. The decision to opt for care home services was often portrayed as a professional decision, but the selection of a specific home was fraught with dilemmas- they did not feel themselves to be ‘informed consumers’. The views of the older people themselves did not seem to be always actively sought- they were sometimes dismissed, or the older people themselves opted out of the process, and this resulted in a paradoxical situation of people wanting to find some where their relative would be happy, yet not involving them in the process of decision- making.

The staff view

The hospital nurses’ responses indicated that there were no standarised approach to dealing with this process- discussions, if they occured, were ad hoc, fragmented and arose only if the older person initiated them. These initiations, however, did not seem to occur very often, with the staff reporting that they did not welcome discussion or invite it- one nurse described older people as having ‘made up their mind to accept their fate, and they do not see the point in discussing it-they only become distressed’. One nurse did, however, indicate in a written response that older people might not openly invite discussion and that sometimes nurses have to encourage them to talk- ‘Sometimes patients do not openly ask for advice or support, but its up to the nurse to spot the signs of anxiety and to approach the subject casually’. Where nurses did give examples of having talked to older people about their impending move they described these conversations as taking place while they were doing other things with the older person, such as helping them to dress. This approach avoided making a ‘big thing’ out of discussions as being to ‘cheer up’ older people.

The nursing staff felt that they knew little about care homes, and could not offer much support. They were not clear, for example, about the difference between the nursing and residential care, about processes of inspection and registration, or about how such care was financed. They also felt that this was not part of their job to know these things, as other staff ( for example social workers) were in charge of the process. In addition, there was some degree of hostility or suspicion towards the independent sector, particularly privately run homes, which were described by one nurse as ‘just in it for the money’. Some nurses had worked in private homes as relief nurses and reported that the standards of care they had seen were low, and there was a reluctance to collaborate with staff from these homes. One nurse recounted a situation where a care home had asked for some information about a patient, but she had been reluctant to provide it:

…it seemed like laziness and should not have be assessing them for themselves. As their care will be completely different from a wards it seemed like a cop out.

Social workers had more contact with care homes, and more knowledge of the systems of regulation and funding care, but this expertise did not necessarily give them a feeling of control over the process. They felt that they were responding primarily to pressures from medical staff to organize discharges and did not have time to spend with patients discussing’ their choices and preferences. They talked about their professional skills in providing support as being eroded by their administrative role in processing assessments and arrangements for care. One social worker described her role as being driven by these demands:

I do not spend the time I used to – it’s just you get a message from the medical staff- this one’s to go out, and you just sort out the paper work and may be talk to the family. Sometimes I do not even get to see the client.

Medical staff, however, felt that their role was mainly in making discharge decisions and deciding the level of care required from a medical point of view. Their concern was governed by Social Service Department financial considerations. They talked of their concern with patients who were waiting to come into hospital, which had to over-ride their concern with those who had received treatment and who had no further need of acute care. When asked about providing support for older people moving into a care home they reported that they expected that social workers and nurses would provide the necessary support and advice to patients. This was partly because they felt that it priority- but also because of the way in which their time was managed and their contact with patients was organised. As one doctor put it:

We see people on a round or at appointments and then we go away. Once we have told them where they are going to go, we disappear, and if they want to think about it late or discuss it after they have had a think about it, we were not there, but the nurses and social workers are more around.

Chapter:5

Conclusion and Recommendations

This research suggests that the apparent stoicism of older people moving into a care home can mask feelings of loss and anxiety. If nursing staff wish to support older people through this transitional process, then they may have to be proactive in initiating discussions rather than waiting for older people to do so. Such an approach, however, must be carefully negotiated with older people- some may not wish to discuss their feelings when offered the opportunity to do so. Such discussions will need to be informed, and there is a need for nurses in hospitals to learn more about the care home setting, and to reflect on some of the assumptions that they may make about the independent sector. Understanding how care homes work may help nurses to encourage older people to think of themselves as people with choices, and working through their personal preferences for activities and lifestyles may well encourage this. We would suggest, therefore, that attention is paid to ways in which nurses can learn more about the care homes, and how they can encourage older people to make active decisions about their move.

This will need to be based on a systematic approach, such as formal assessment and review procedures, rather than rely on ad hoc initiatives. Developing a formal assessment schedule which is written with patients and which focuses on life styles preferences may go some way towards supporting older people in exercising and expressing preferences, and if this were to accompany them to the care home it would provide valuable information for staff there. An extension of this study would involve the development of such a schedule.

In addition, the data suggest that there is some confusion between nursing staff, medical staff and social workers about who is responsible for which aspects of the discharge procedure, with each professional group assuming that another has chief responsibility or input. For the future development of discharge processes, multidisciplinary teams need to clarify exactly what responsibilities each group has , and ensure that contact with older people is documented to reflect this. As Penhale (1997) has argued, multidisciplinary working in discharge planning is fraught with problems which arise from different goals for practice, and different form of organisational power across professional groups, but such negotiations is essential if older people are to be given the support that they need at a time of great change and potential stress in their lives.

Happiness in the contemporary world | PHIL 3010 – Science and Spirituality | Walden University

Review this week’s readings (Preface, Chapter 1, Chapter 2, and Interlude 1) in the course text Has Science Displaced the Soul? and think about how different spiritual traditions and modern scientific thought view the concept of happiness.

Listen to the Radio Laureate Interview with Dr. Kevin Sharpe: “The Voice of the Author.”

Consider different aspects of happiness on which spiritual and scientific thinkers might agree or disagree.

Reflect on how your own exposure to the modern media has influenced your ideas about what happiness is and how it can be attained.

With these thoughts in mind:

By Day 3

Post a 2- to 3-paragraph response in which you share one point about happiness where spiritual traditions are in conflict with science and contemporary life, and one point about happiness where spiritual traditions and science can be in concert with one another. Then, describe the role of advertising in our contemporary world and discuss what part you think it might play in people’s perceptions of their own happiness. Support your assertions by making at least 2 references, in proper APA format, to your course readings.

The Impact of Nursing Shortage

The Impact of Nursing Shortage

The Impact of Nursing Shortage

The Impact of Nursing Shortage Healthcare is one of the fundamental sectors as far as any society is concerned. Nurses and the entire nursing discipline facilitate the provision of quality healthcare. Outpatient wound care is one of the elements of healthcare, and since most of these cases are outpatient, most governments and stakeholders have worked hard in ensuring that quality services are provided. Shortage in the nursing department is a common phenomenon in most parts of the world. A shortage occurs when the demand for nurses in different health institutions is higher than the numbers of available qualified nurses. Such a shortage, inevitably, affects most of us in one way or another, since accidents characterize most of the daily activities. The accidents in the workplace, in homes, and on the roads are an implication of how important outpatient wound care is to society. The few nurses in most hospitals are forced to work under pressure due to the increased number of patients, and having experienced the effects of this shortage first hand, I can attest that it is important to improve the nurse to-patient ratio. Minor injuries could pose a lot of danger to a persons health due to delayed medical attention, which could be caused by long queues in health facilities. The article points out the different genuine myths about nursing shortage, but also highlights the undesirable effects of understaffed health facilities as far as patient care is concerned. The article also highlights the possible causes of the shortage of nurses in different countries, where migration from source country is highly likely to cause shortages there. The quality of healthcare is dependent on the ability of the nurses department to deliver quality outpatient services. References Goulette, C. Nursing (Job) Shortage. New Grads are finding the Job Hunt Tough. Advance for Nurses. Issue January 18, 2010. Christiane Wiskow, Tit Albreht, and Carlo de Pietro.How to create an attractive and supportive working environment for health professionals Health Systems and Policy Analysis.

Resilience and Mental Health Care in College Students


Introduction

When we think about resilience and mental health, we want to be able to understand that life has many challenges and barriers to overcome that causes setbacks for each individual. When something goes wrong in our lives, we want to be able to bounce back in a recovering way that conquers each obstacle we face so that we can live within a positive mental health frame. When having resilience, you are able to have strength from within that helps you rebound from any setback or challenge. This may include “job loss, an illness, a disaster or the death of a loved one” (Mayo Foundation of Medical Education and Research, 1998). For myself, it is finding resilience within academia and understanding the many identities that students face when they bridge from high school to university. Within this paper, I want to discover how to have the ability to overcome obstacles, challenges, and barriers by using the academic planner and understanding the many identities we as students face in our everyday lives as we discover who we are and how we fit within society. Also, how to protect your mental health from the various conditions such as depression and anxiety, two very common illnesses that many students who enter into university develop due to the overwhelming need to please others in order to fit into their social roles. This paper will look at social institutions and how the government, school and health care system encourages us to think and live in a particular way that helps to maintain a social order in our society. Also, critically looking at what is the normal and the pathological and understanding the idea behind it.


What is Resilience?

To define resilience is to have “the ability to overcome difficult challenges that individuals who are resilient are able to cope with when they are exposed to stressful life situations” (Southwick, Bonanno, Masten, Panter-Brick, Yehuda, 2014). Another aspect of resilience is to also have the ability to not only cope and move forward with their challenges, but it also builds on strengths from their many experiences where they are able to heal from life stressors and challenges in the future. According to the Centre for Addiction and Mental Health (2007), “the ability to be resilient in the face of adversity involves a number of factors such as being empathetic, have good communication skills, problem solving skills, and be able to set goals” (Centre for Addiction and Mental Health, 2007). Part of being resilient is having a strong hold on your mental health which can be a part of having a positive mental health. In promoting mental health, it means to have effort in increasing positive mental wellbeing, therefore building resilience.

Resilience is impacted by multiple factors such as “characteristics of the individual, families and communities or environments” (Centre for Addiction and Mental Health, 2007). These factors affect the intensity of these risks and protective factors that determines the likelihood of someone becoming resilient. With the individual family and environmental factors that bring about resilience, there is a benefit to promoting protective factors and reducing risk factors. Social supports come from “positive peers, supportive teachers, and other adults, as well as immediate family” (Centre for Addiction and Mental Health, 2007). On a macrosystemic level, community factors such as “good schools, community services, sports, cultural factors, spirituality and religion, and lack of exposure to violence, contribute to resilience” (Centre for Addiction and Mental Health, 2007). There is value in the more individualistic approach to understanding the relationship between resilience and mental health, however, it only tells a small part of a much greater story. For myself, I look upon building resilience when I find myself coming into a time of need. Making connections and having good relationships with family members, friends, and others are important to me. I accept help and welcome the support givesn from those who show that they care and will listen to me during those stressful times. Having that open ear strengthens my resilience. What I also do to uphold my resilience is learning how to interpret a situation where I change how I respond to it better. I would look beyond the present situation and into the future where it gave me a more positive outlook and helps to build academic resilience to assist me during my educational years.


Academic Resilience

It is important to place the term resilience into a specific context. In the social sciences program, specifically health studies and gerontology, we place a lot of emphasis on context and historical context. This determines how we think and live, especially in the now where historical context matters most. The particular social context we are in matters, where talking about something in University is different than speaking about it in high school. This is where we modify the term resilience into the term academic resilience. It connects to our notion of identity and how our identity is constructed. With that, there is no singular identity, we have multiple that get constructed all the time. Compared to a couple hundred years ago, we had a relatively fixed identity. For example, where we were born, our family, what our families did, would all be connected to us. The hard part of this process of identification is when the identity you are constructing becomes an object. If conforming to a label is a way to identify yourself, it stops being a process that you can control and becomes an object that controls you. An example of this is bullying and allowing what you are being labeled as define you to the point of you believing it to be true.  The main point is having awareness of the identity constructed and becoming more aware of how you are constructing these identities. Doing so can manage the way you view and talk to others where you can educate and help them support their own identities at the same time.

In relation to the articles where part of the research is understanding why the students are struggling in regard to their mental health and why this may be the case, one way of thinking about this is from a University point of view. We are just students and that is our primary identity that we construct while attending school. We also have other identities that are happening around us all the time such as being a part of a family as a son or daughter or being a parent ourselves. The key tensions within the article was that what students were experiencing was balancing a student identity with their family identity. If families did not understand the pressures of what it means to be a student, the student may be in a lot of stressful trouble.

From my own personal experiences with finding my identity and seeing how the schools handle the transition, I find that it is challenging for first year students to deal with the stressors of managing their family identity and their student identity. When students such as I add in a third identity which include maintain a job on top of everything else and fourth identity of maintain friendships, the stressors almost become life destructing. The academic resilience planner that was completed for lecture has been a tool used to help individuals maintain their identities and remember their purposes in each one. The planner has helped myself in managing my anxiety and stressors in which I was able to successfully balance and manage my multiple identities that I have within my own networks and kept myself grounded in times of crisis. I have also had the experience of using a similar planner when assisting clients who are experiencing their own form of identity crisis and anxieties in which has successfully worked with them so that they are able to care for themselves and others with positive mental health.


Critical Perspectives of Resilience and Mental Health

As discussed in lecture, every social institution that was spoken about such as the government, school and health care system, encourage us to think and live in a particular way that helps to maintain a social order in our society. To think this way is valuable in how we construct ourselves to our identities. However, in other cases, a society without social order is destructive. When looking from a critical perspective, there is a need to critique the negative impacts of that social order. Within our social institutions such as the educational system, it is designed to advantage some people and disadvantage others.

From a critical perspective, the readings and lectures look at it in ways where social institutions encourage a particular social order that advantage some people and disadvantage others. In the case of health and mental health, it is referred to as the normal and the pathological. This idea tends to take all the differences among a population and average them with a mean. It was determined that what might be normal is not actually a representative of the diversity among that population. An example of this that was discussed in lecture would be the body weight of children as they are developing. The argument here is that the idea of the normal and the pathological are backwards. For example, in lecture we spoke about a French theorist within the medical sciences. This theorist spoke about the knowledge being produced about people’s health and tried to come up with a set of norms among a population of people. His argument is what gets constructed as normal which is the average across differences, end up being pathological. Therefore, the argument is that normalizing how we understand things is valuable in terms of creating mechanisms to try to encourage people to follow a certain social order but intend to pathologize difference.

With connecting mental health and resilience, people who have a different kind of mental health orientation, living with a mental illness, or have challenges, makes an argument where they  are not pathological. It is just ways of inhabiting the world and it goes against the order that is constructed. Trying to destigmatize and normalize different ways of living in the world is done by looking at these movements and groups of people who are trying to shift the structures in the way people think about mental health, and what we consider to be normal and pathological. This is where having self-acceptance plays an important part with having resilience. There is always this pressure that individuals need to be more than what they already are, and this pressure ends up holding people back. When we realize that we are more than those pressures, it allows us to do the things that we want to do.


Conclusion

Having resilience is an essential tool to master in our everyday lives. I find that for myself, having resilience has helped me overcome challenges that I have faced, more so over the four years I have spent at McMaster. Previously I was a student at Mohawk and transitioned from a college student into a university student. The first-year transition was extremely difficult for me as I had nothing to prepare me for the culture shock and advanced educational expectations than what I was used to with coming from a local community college where standards were lower than at McMaster. I felt very lost mentally and emotionally, struggling to understand my place not only at school, but in the world.  Without knowing it, I’ve used resilience to overcome the challenges and barriers I was facing over the years I was a student at McMaster. Building resilience is a journey and each approach is unique to every individual. What has helped me is making connections and building a strong family network that has supported me throughout my journey in university. It has helped establish my identity where I have been able to be a student, friend, girlfriend and daughter without feeling the pressures to favor one over the other. I encourage the use of the academic planner so that others are able to find truths within themselves and be kept grounded in times of crisis and to not allow those social institutions such as the government, health care system, and schools to label us and expect us to confirm to those identities in order to feel that we are worth something if we do.


References