The Effects Of Cultural Conflicts In Ethiopia

Ever since the first cases of what eventually came to be known as AIDS were diagnosed in the early 1980s, people with HIV/AIDS have been stigmatized. Over time, there have been many misconceptions about this disease. Even though there have been many discoveries, and treatments for HIV have improved over time, there are still many people who understand very little about this disease. This lack of understanding, along with fear, misinformation about how the disease is transmitted, and “moral” judgments made about the types of people who contract HIV, all have led to stigmatization of, and discrimination against, people who are living with HIV/AIDS. Understanding the stigmatization of people with HIV/AIDS is an important social justice issue because that stigmatization can result in people with HIV being insulted, rejected, gossiped about, excluded from family and social activities, fired, and even jailed. People with HIV are no different from people suffering from other chronic diseases. Instead of being alienated, they have a right to be treated with fairness, respect, and dignity.

Education of HIV/AIDS is very important to help prevent from becoming infected with this deadly disease. There are many factors that are being looked at that may be associated with the affect of the transmission of HIV such as, gender relationships, social exclusion and poverty, etc. These issues happen every day and health care providers must help those infected with HIV/AIDS to start treatment right away (Mayo Group, 2010). A national health policy must formulate different guidelines what will enable the policy to help the government govern the public. This stage is really important to help bring health care policies together.

The film describing an ordinary woman Noerine Kaleeba devoting herself fighting social stigma around AIDS in Uganda is a powerful scene. Her personal account of seeing her husband dying from AIDS propelled her to fly to Geneva to meet with Jonathan Mann, the leading researcher in the global AIDS program. When she arrived at the WHO building, she was rejected to meet with Mann. However, her emotional response caught Mann’s attention and when she sat down with Mann, he told her that her husband is going to die. But Mann asked Kaleeba “there is a prejudice that is attached to this disease that we have to fight, and will you help me fight it?” Kaleeba later became the co-founder of the AIDS activism group “The AIDS Support Organization,” a group that provides care, support and counselling as well as community education for prevention in Uganda. In this scene, Jonathan Mann recognized an important social factor of the disease which is that AIDS is attached to a serious stigma and discrimination. Due to the fact that there is

Of the 35 million people living with HIV in the world, 19 million do not know their HIV-positive status. Adolescent girls and young women account for one in four new HIV infections in sub-Saharan Africa. Women are much more vulnerable to HIV, tuberculosis and hepatitis B and C than the general public. Which is supported by this excerpt from a recent AIDSTAR-One regional report “Women and girls often face discrimination in terms of access to education, employment and healthcare. In this region, men often dominate sexual relationships. As a result, women cannot always practice safer sex even when they know the risks involved. Gender-based violence has been identified as a key driver of HIV transmission in the region.” (Ellsberg, Betron 2010) Many children are affected by the disease in a number of ways: they live with sick parents and relatives in households drained of resources due to the epidemic, and those who have lost parents are less likely to go to school or continue their education. Studies in the regions of Southern Africa and South-East Asia have found HIV/AIDS to negatively impact both the demand for and supply of education. Orphaned children are either pulled out of school or not enrolled at all due to the financial constraints of

With the help of government programs such as the ADA (Americans with Disabilities Act) as well as multiple other methods of sociological research and social justice work, there have been shifts toward better understanding this disease, those which are living with it, and the societal impact one’s own prejudices can make toward an individual living with AIDS. However, discrepancies still exist within how to properly educate others on the disease, how to recognize it as a disability within the context of our society, and how we must reconcile stigmas that play a role in plaguing any sort of positive conversation on the topic. With well-informed citizens on the issues of HIV and AIDS patients, not only can we reduce the stigma associated with the illness, but also work toward medical advancements that assist those living with HIV in a nondiscriminatory manner.

In The Invisible Cure, Helen Epstein talks about why HIV/AIDS rate is so high in Africa compared to the rest of the world. Through the book, she gives us an account of the disease and the struggles that many health experts and ordinary Africans went through to understand this disease, and how different African countries approached the same problem differently. Through this paper, I will first address the different ways Uganda and Southern African countries, South Africa and Botswana in particular, dealt with this epidemic, and then explain how we can use what we have learned from these African countries to control outbreaks of communicable disease elsewhere around the world.

The infection rates of HIV in women ages 15-24 is approximately twice as high as men in the same age group. Access to sexual and reproductive health services in Africa is restricted by the gender inequality, stigma and discrimination in the face of high HIV/AIDS prevalence. The study is limited to 2 cities, Uyo and Calabar; major centers of HIV/AIDS response. Interviews reveal that large numbers of people, especially from rural regions, are improperly informed and unaware of the nature of HIV/AIDS. An outreach program displayed HIV prevention messages, but the signs were in English. Access to ART can be difficult. Poorer women cannot afford repeat visits to clinics. Societal issues are present; HIV/AIDS stigma is widespread and families will outcast individuals, denying them of any support. The study also showed a declining confidence in ART as a form of treatment. Respondents reported cases of those on HIV/AIDS treatment who developed further infections. The article displays the need for better education and programs to help people access treatment for

Looking through the theme of Development Issues of women and health on women’s health, specifically empowerment of women and improving maternal health, I focus on the mothers2mothers organization. These constraints are being limited for the sake of this paper to the stigma of HIV positive mothers and the discriminatory medical services that are then placed on HIV positive mothers in South Africa. This raises the problem of mothers identifying as HIV positive in South Africa as they are then being stigmatized, therefore I will be asking, how does the organization takes steps in order to help protect the women from stigmitation as they are in the prevent[ion] mother-to-child transmission (PMTCT) program? Analyzing the constraints of participation of HIV positive mothers leads to the stigma associated with HIV/AIDS infection, the lack of women’s empowerment, and the deficiency of appropriate and culturally sensitive clinical support services, even in facilities providing PMTCT services, means that many women go through their ordeal alone, confused and afraid.

The relationship between Aids and African culture can be seen in various ways, values in African culture on marriage, fertility are often seen, however, more recently education and social structure have also played a role culture.

People with AIDS are concerned about some of their rights that they might lose. Some of the consequences that those with AIDS have are restrictions on international travel, housing, employment, medical care, and health care insurance (Comprehensive). One of the biggest fears of people in the community is acquiring the HIV/AIDS disease. Because of the terrible effects of HIV, community members tend to have some concerns about those with the disease. People who are diagnosed with AIDS are usually highly discriminated against. It can be very difficult for people with AIDS to find a job, because they are constantly being denied (Comprehensive). They also have problems with being restricted or denied access to education, health, and social services (Comprehensive). Governments are held accountable for the way they treat those with HIV/AIDS and how they deal with their rights. The government is responsible for not violating the rights of those affected with HIV/AIDS. There are certain rights that cannot be taken away from those with AIDS. These are the right to be free from torture, slavery, or servitude, the right to a fair trial, and the right to freedom of thought (Gruskin, 2002). There will always be discrimination, but there needs to be a better balance of the protection of those with HIV/AIDS, and the community members, protecting all human

Even after 30 years for some the stigma attached to HIV and AIDS often can lead to those who suffer from the illness as being second class citizens. The idea that those who have HIV brought upon themselves through “bad behaviors” can result in some people not seeking help or when they do they wait until the disease has progressed. However, the center for disease control considers HIV to be a focal point in the Dominican Republic, and one of the major concerns is how health officials can lower the number of new cases the country sees each year. One must understand that the rise of deaths from AIDS-related complex can mean an increase in mortality across the board creating a domino effect within the health system. Therefore education and awareness could change the health narrative by using preemptive measures. Also, those who are tested regularly and seek help quickly are those who are most likely to live full long lives.

To address the communication problem, we must understand that there have been many alternative names that human-beings have given to HIV/AIDS and the amount of information and knowledge of the sexually transmitted disease has gone into overload since the huge epidemic, primarily during the twentieth century. This overload of information has caused many to disregard the issues and as an ending result caused many to focus on the issue and factors associated with HIV/AIDS as much as many once did in the past. Although HIV/AIDS no longer dominate the headlines, we must wonder are health professionals and AID advocates still giving out all the clear signs because it is apparent that HIV/AIDS are still a danger to society.

Many immigrants amaze about how their home country culture changes when they return after living abroad for several years. However, Jacqueline Novogratz was surprised about the ways that Duterimbere changed from its beginnings to its current state in Chapter 12 of The Blue Sweater. When I went back home, Ethiopia, last summer, June 2016 after living 4 years in the U.S.A, there was a different place than it was previously.

Sub-Saharan Africa is the region of the world that is most affected by HIV/AIDS. The United Nations reports that an estimated 25.4 million people are living with HIV and that approximately 3.1 million new infections occurred in 2004. To put these figures in context, more than 60 percent of the people living with the infection reside in Africa. Even these staggering figures do not quite capture the true extent and impact that this disease causes on the continent. In 1998, about 200,000 Africans died as a result of various wars taking place on the continent. In that same year, more than 2 million succumbed to HIV/AIDS (Botchwey, 2000).

There are HIV-related stigmas and discriminations that refer to the prejudice, abuse and negativity that is shown towards people living HIV and aids.in many countries with available data, over 50%of people have been said to have shown discriminatory attitude toward people living with HIV and AIDS. These stigmas have made people living with this