Doctor Patient Relationship Essay

In the book “The disability rights movement” I learned the history and process people with disabilities have been going through in order to obtain an equality of rights in the United States. The book was written by Doris Zames Fleisher and her sister Frieda Zames as a way of raising awareness of the reality of people with disabilities. Frieda Zames an activist in favor of the American disabilities act, wrote this book to tell the story of civil rights movement and to make people aware of the struggles that people with disabilities go through at the same time raising the word for equality. The book demonstrates how grievances regarding medical issues can be addressed in a democratic society by giving examples such as the life of President Franklin D. Roosevelt. As a significant figure in this movement, Franklin D. Roosevelt was the first president with disabilities, who contracted polio eleven years before he became president. He was a significant figure in the movement because he served as an example of the capabilities a person with a disabilities can have. He was also an advocate of

Despite this overall attitude of how individuals with disabilities need medical and educational interventions, there are also many other beliefs that some Americans have regarding disabilities. Americans’ attitudes toward disabilities are similar to Pacific Islanders, Philippines, Chamorro, and many other cultures due to Americas cultural diversity. America is likely to have Americans with the exact same views as these cultures due to the nations

In the United States today, there are over fifty-one million disabled adults and children. Throughout our nation’s history, we have not allowed the best treatment and care for these numerous citizens. But, in the recent past, the government has passed laws, made exceptions, and thoroughly tried to provide accommodations to these people with special needs. While this is true, America, as a whole, still views this group as strange or different. Even though this is exceptionally normal, it is not correct. The United States needs to be opened up to the truth about their fellow American citizens. The people of America ought to understand that these disabilities affect not only those who are disabled, but that it affects the family and friends

Douglas C. Baynton argues in his article, “Disability and the Justification of Inequality in American History”, that the concept of disability is culturally constructed and has been paid little to no attention to throughout history. He also argues that the term disability plays an important role in justifying discriminations against minority groups, based on gender, race, and ethnicity. He states that “Disability has functioned historically to justify inequality for disabled people themselves, but it has also done so for women and minority groups. That is, not only has it been considered justifiable to treat disabled people unequally, but the concept of disability has been used to justify discrimination against other groups by attributing disability to them.” (Baynton 94) He used women’s suffrage, African American freedom, and immigration restriction as examples to show how disability played an essential role in illustrating how minorities who were labeled as disabled were treated with discrimination. As they were labeled with disability, discrimination against them became justifiable, which ultimately proves that discrimination against disabled was thought as justifiable and were looked over.

Individuals with disability have had a long history of maltreatment in America. From being thought of as possessed individuals in need of exorcism, targeted for heinous experiments, unknowingly sterilized, being labeled imbecile, feeble minded, and retarded, to being shipped off to state schools or mental asylums, those with disabilities were given no consideration as a valuable and able to contribute member of society. In a speech to congress, Frank Bowe, a highly educated deaf-man highlighted this claim by stating, “we are not even second-class citizens, we are third-class citizens” (Bowe, F. 1977--need citation), and Jim Cherry (2001) furthered the ideal in his words, that prior to “1970 we [disabled citizens] had no right to education, to employment, to transportation, to housing, or to voting. There were no civil rights laws for us, no federal advocacy grants. Few people looked beyond our medical needs” (Cherry, J.L, 2001 http://www.raggededgemagazine.com/0701/0701cov.htm). Section 504 of the Rehabilitation Act of 1973 attempted to fundamentally change how disabled people were reguarded.

Americans with disabilities make up the largest minority group in the United States. Approximately fifty million people in the United States live with physical or mental handicaps. This minority group is unique in that it is made up of people from all socioeconomic classes, genders and races. Mental and physical impairments do not discriminate. As with other minorities, Americans with disabilities face unique challenges and discriminatory behaviors. For centuries, disabled people had to battle irrational fears and stereotypes due to the lack of medical understanding. The first demand for equal treatment for disabled people came in the 1960s. The struggle for disability rights has followed a similar pattern to many other civil rights movements – first negative stereotypes must be challenged, followed rallying for political and institutional change and lobbying for the self-determination of a minority community. As a result the examples of the African American civil rights and women’s rights movements encouraged the disability rights movement, and after decades of campaigning and lobbying, the Americans with Disabilities Act (ADA) was passed in 1990.

Bridging this gap in accessibility of access of care is a difficult mission. Establishing a culture of community participation and communication is need between healthcare providers and disable patients. We have laws in places, like the Americans with Disabilities Act (ADA), which is a wide ranging federal legislation intending on making American society more accessible to people with disabilities (ADA,

After the world wars and Vietnam War, there were many disabled American veterans who faced challenges and prejudice they had not experienced before. Alongside those fighting in the Civil Rights Movement were disabled veterans and other people with disabilities. They too were fighting against inequalities and discrimination. The Disability Rights Movement occurred due to several issues rooted in structured inequalities. The Civil Rights Act of 1964 was an example of inequality built into legislation as it prohibited discrimination based on “race, color, religion, or national origin”(Cornell), but did not address discrimination based on disabilities. Inaccessibility and negative societal views excluded those with disabilities from their rights. There was a need for a policy written specifically for the protection of persons with disabilities.

How does this social construction of disabilities impact institutional policies, and societal and individual behaviors regarding disabilities? In other words, how have people with disabilities been marginalized in the past and present at those three levels? Please be specific and provide examples to support your answers.

All they want is to take part of society as a normal individual. The disability-movement has fought for the disabilities rights throughout the years and has achieved goals such as accommodation of architectural infrastructures to serve better people who are physical impairments. The public policies have been great accomplishments because it has helped people with disabilities to be part of society. The disability-movement points out the healthcare finance policies have taken freedom away from the disability community, “ Health-care financing policies force disabled people into Institutions and nursing homes rather than funding independent living. Income-maintenance and public health-insurance policies include “disincentives” that penalize disabled individuals for trying to work productively.”(p.4). The government has done a great job on protecting disabled individuals’ rights. However, the health-care system has isolated this group even more by restricting the level of productivity that they have within the system, as a result this medical model marginalizes this group of people and this program available for this community does not fully address their issues.

All people who have brown hair are not alike. All people who have disabilities are not

In our report we show the importance of patient provider relationships and the impact of the patient centered relationships.

The social interaction is an integral part of everyday life of each individual, which is learned from the early childhood and is innate in its nature. It includes the social exchange of information, the ability to communicate, decide, and take responsibility for one’s action. The routine work of healthcare professionals includes the information exchange on an everyday basis. The excellent knowledge of primary disciplines necessary for the practice is crucial for the healthcare professional; however, one can encounter the difficulties without the deeper understanding of ethical principles of communication in the healthcare environment. The book “Health Professional and Patient Interaction”” by R. Purtilo, A. Haddad, and R. Doherty introduces the readers with the basic ethical principles and behaviors in the healthcare setting. The key points that the healthcare professional has to practice to achieve success and harmonic professional relationship with the patient are: respect in all circumstances, the ability to listen, the readiness for challenges, and care with empathy to the patient situation beyond any limits.

Disability Inequality is an issue which society often ignores but is an alarming topic. People tend to assume they are ill-equipped mentally since they are disabled physically. It has immense effect on people with disabilities.

A twist on the "patient's perspective" approach is to describe a time when medicine failed to save or heal someone close to you. The purpose of this tactic would not of course be to rail against the medical profession, but rather to show how a disappointing loss inspired you to join the struggle against disease and sickness.