Ethics & Society Newsfeed: World AIDS Day 2017

World AIDS Day, December 1, 2017
National Aids Trust (NAT)

“World AIDS Day takes place on the 1st December each year. It’s an opportunity for people worldwide to unite in the fight against HIV, to show support for people living with HIV, and to commemorate those who have died from an AIDS-related illness. Founded in 1988, World AIDS Day was the first ever global health day.”

The theme of this year’s World AIDS Day, as promoted by NAT,  is “Let’s End It.” This year, NAT is asking everyone to join the fight to end the negative impacts of HIV including isolation, stigma and HIV transmission. According to the World Health Organization (WHO), there were 36.7 million people living with HIV at the end of 2016 and 20.9 million people living with HIV were receiving antiretroviral therapy globally. This year, WHO is advocating for access to safe, effective, quality and affordable HIV services, medicines and and diagnostics other health commodities for all those in need with their slogan “Everybody counts.”

Please visit the World AIDS Day website for more information about the history of the day and how to get involved, support and show solidarity with the millions of people living with HIV.

HIV/AIDS in the News

World AIDS Day 2017 Theme, Facts and Events: Everything You Need to Know

World AIDS Day: I have HIV and I’ll work to end this epidemic until I no longer can

The Global HIV/AIDS Epidemic Explained in 3 Charts

The Global Gag Rule Impacts Hard-Fought Progress On HIV/AIDS Relief

On World AIDS Day, “encouraging signs” seen in fight against HIV

NIH Statement on World AIDS Day 2017

World Aids Day 2017: Donald Trump breaks tradition by not mentioning LGBT community in proclamation

It’s World AIDS Day and this is what the White House page still looks like

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What Does Silence Say?

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STUDENT VOICES | CHYNN PRIZE SECOND-PLACE WINNER

By Amy Endres

There had never once been a public opinion poll done in El Salvador until Ignacio Martín-Baró, a Jesuit, set out as the only doctoral-level psychologist in the country to measure the opinion of the people in the 1980s.[1]  He knew this would be difficult.  He had studied at the University of Chicago, and he was certain that he would need to practice very differently than how he had been trained.  But he had still been unprepared for just how difficult it would be.

Much of Martín-Baró’s early conclusions were made on the fact that very few people would speak to him.  Only 40% percent of the rich felt safe enough to speak their opinion.  And the poor? Less than 20% of the poor would do the speak to him.[2]  Less than 20% would speak to him about their lives, what they thought of the government, or anything that could get back to someone who could hurt them.

In his case, silence stood for more than an inconvenience to answer a pollster.  It stood for more than a passive distrust of someone collecting data.  In his case, silence told a story of gripping fear, of generations of pain, of mothers mourning children slain by an oppressive and violent government.

Silence says a lot, and it’s important that researchers take that silence into account.

I do not present my essay from El Salvador, though, much less an El Salvador in the throes of civil war like my introduction remembers.  Instead, I present my essay from the United States.  Martín-Baró was attuned to the differences between the countries.  He remarked to an American colleague once that, “In your country, it’s publish or perish. In mine, it’s publish and perish.”[3]  Indeed, Martín-Baró would later be killed, one of eight martyrs, in November of 1989.

I do not propose that he was mistaken.  He was an American-trained researcher after all; he would know the dynamics between the countries.  There is far more protection in the United States, particularly for the researchers today, than there was in Martín-Baró’s time and region.  However, I do want to turn my gaze to those who cannot freely speak their mind in the United States, and posit that researchers can (and, I argue, should) take on their behalf, if they are to act in the heroic way that Martín-Baró did.

What does silence say in the United States?

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“She Can’t Help The Choices She Makes”

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STUDENT VOICES | CHYNN PRIZE FIRST-PLACE WINNER

By Madeleine Cardona

I will never forget the day my mother got diagnosed. I could swear that just yesterday I was thirteen years old waiting anxiously to be called in from the waiting room of some fancy New York State doctor’s office. I was young, but I had some idea of what was going on. I knew my parents and I were there because they were going through a divorce and fighting for custody of me. What I did not know was that we were about to endure a court-ordered psychiatric evaluation and that the results were going to change my life forever.

“Madeleine, your mom is very sick,” the psychiatrist attempted to explain to me. I did not understand. I did not know a sick person could look perfectly healthy. “It’s not a physical sickness, it’s in her head. She has a mental disorder called Paranoid Schizophrenia.” She went on using big words to explain how my mother’s brain “wasn’t like other people’s brains.” I sat there listening closely, hanging on every word the woman was saying to me. “She can’t help the choices that she makes, it’s not her fault that she is the way that she is. She needs help.” Every day since that day in the doctor’s office, that remark replays in my head over and over. “She can’t help the choices she makes.”

That is what gave me the most trouble. I sat around for years and years watching the choices that my mother was making, unable to intervene. If she cannot help the choices she makes, why could my dad or my mother’s other family not make the choices for her? Why could nobody make her take medication? I eventually learned that it was because my mother was sick, but “not sick enough.” The court ruled in favor of autonomy and said that my mother still had the right to make her own medical decisions. According to them she was functional and was not posing an immediate danger to herself or others. I understand autonomy. Autonomy is defined as “a principle in which a person should respect the rights of other individuals to freely determine their own choices and decisions” (Jonas). I understand how important free will and the ability to make choices about your own body are. It is hard for me, however, to understand how you can continue to honor a person’s right to make their own decisions, when every decision they make is only hurting them. It is hard to sit there, as a loved one, and not want to just make them take the medication they need to get better, or force them participate in that research study that just might help.

Continue reading ““She Can’t Help The Choices She Makes””

Ethics, Undocumented Immigrants and the Issue of Integration: Making a Better Life for Everyone in New York City

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STUDENT VOICES

By: Yohan Garcia

This essay is in response to the Carnegie Council for Ethics in International Affairs video clip “Nisha Agarwal: IDNYC & the Undocumented Community.”  

According to a study conducted by the Migration Policy Institute (MPI), an estimated 643,000 undocumented immigrants live within the five boroughs of New York City. Advocates of the New York City Municipal ID card hoped that government-issued photo identification would bring many of those undocumented immigrants out of the shadows. With the newly elected President of the United States, Donald Trump, many are wondering whether the NYC Municipal ID was the right thing to do as the cards can put undocumented cardholders at greater risk of being harassed by government authorities and even of deportation.

Nisha Agarwal, Commissioner at the NYC Mayor’s Office of Immigrant Affairs, argues that the NYC Municipal ID card has helped many undocumented immigrants do things such as pick up their kids from school, access public and government buildings, interact more easily with police officers, and open bank accounts. Furthermore, the Commissioner argues that the Municipal ID has helped many undocumented immigrants increase their sense of belonging to New York City and to the United States. Given that sixty percent of NYC’s population is foreign born and less than half of the city’s population has a driver’s license, the Municipal ID proves to be an effective legal response to cope with the need for identification in NYC.

One of the biggest misconceptions about undocumented immigrants is that they take job opportunities away from American citizens. Many believe that immigrants do not pay any taxes and that they do not want to assimilate to the United States. However, studies conducted by the Pew Research Center suggests that these opinions are a product of anti-immigrant context which has been sustained and reproduced by the political climate. It is both unethical and immoral to punish individuals for choosing to migrate to another country without having the proper documents. The United States takes in a certain number of refugees per year, would it not be morally wrong to ignore and punish those already living in the country?

Continue reading “Ethics, Undocumented Immigrants and the Issue of Integration: Making a Better Life for Everyone in New York City”

TEDxFordhamUniversity: Lesson in Bioethics Given by Golden Girls | Dr. Elizabeth Yuko

As one of the most groundbreaking sitcoms of all time, The Golden Girls introduced a range of bioethical issues on the show regarding medicine, the human body and women’s health.

In this TEDx Talk, Dr. Elizabeth Yuko, a Fordham University Center for Ethics Education  fellow and adjunct professor, discusses how influential Golden Girls was, and still is, as a lens for the study of bioethics and its principles using examples from the show’s most notable episodes.

Watch below:

Dr. Elizabeth Yuko is also the Health Editor at SheKnows Media, a women’s lifestyle digital media company operating SheKnows.com. BlogHer.com. HelloFlo.com and STYLECASTER.com. Please visit her website and Twitter page for more information.

Ethical Implications of Victim Blaming in Cases of Police Brutality

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STUDENT VOICES 

By Emily Jenab, M.A.

Another black man has been shot and, subsequently, another case of character assassination post-death has begun.  Alfred Okwera Olango, 38, was killed as he pulled out “a three inch long vape” and allegedly pointed it at the police of El Cajun, California. The shooting of Olango, an “emotionally disturbed” man who was shot after his sister called 911 for help, has already resulted in justifications of why he deserved to die. Yes, he was holding a vape, but why did it look like a gun? Why was he standing like that? Why did he hold his vaporizer between his hands? Efforts to legitimize another murder, and state implicated violence, will be taken. The cycle repeats and ethical and emotional discussions surrounding these murders, along with the issues embedded in police systems, will continue to be ignored.

Respectability politics are pertinent for people of color, and for marginalized persons, the respectability of their very identity is questioned when they are victims of police misconducts. There is, for our cultural purposes, no “good” black man; if he is unarmed, as Eric Garner was, he still deserves to die and his murderer will not be charged. If he is armed in an open carry state, as Philando Castle was, it is asked why he even had a gun, or what he was doing prior to being pulled over. These men – employed, fathers, worthwhile members of their communities – are reduced to “thugs” in the wake of their deaths. As the horrific deaths play across screens, the feeling of inequality and shame arises in some while others choose to dehumanize and delegitimize the lives of victims. Even one’s commitment to serve his or her country is ignored, like the case of Anthony Hill, a veteran of the US Air forces who was killed in Georgia. There is no shield from pervasive racism, even serving our country, something that is normally highly venerated.

Perhaps “bad cops” and those who support them unwaveringly are engaging in some form of culturally disseminated ‘gaslighting’. The methods behind this tactic, normally perpetrated by domestic abusers, can be used to warp reality for the masses. As Shea Emma Fett notes, “every time an obvious hate crime is portrayed as an isolated case of mental illness, this is gaslighting. The media is saying to you, ‘What you know to be true is not true’.” The media, police departments and their ardent supporters present the same message: a victim of police violence becomes a criminal; a father becomes a criminal, a teenager becomes a man and a boy like Tamir Rice, barely 12, becomes a threat.

Continue reading “Ethical Implications of Victim Blaming in Cases of Police Brutality”

Fordham’s Dr. Elizabeth Yuko Address Ethics of Web Self-Diagnoses

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Millions of people use websites like WebMD every day to gain insight on a range of medical issues from cancer to mental health. This practice, or “cyberchondria,” is a new digital phenomenon that has resulted from online databases of free, medical information.

With about 74 million users each month, the information on WebMD provides some with clarity for our most intimate and confusing health concerns, but for others, it could be a source of anxiety. In a recent article published in GOOD Magazine, Fordham University Center for Ethics Education Bioethicist Dr. Elizabeth Yuko addressed the “ethical gray area” of web diagnosis and online symptom checkers.

“Websites and algorithms are not held to the Hippocratic Oath. Because WebMD is a media organization, rather than an individual medical professional, it is not held to the same legal and ethical accountability as individual practitioners,” notes Dr. Yuko. Unlike WebMD, other online communities and health professionals must operate under ethics codes and guidelines designed by organizations such as American Medical Association and American Psychological Association.

As far as legal liability is concerned, Dr. Yuko explained that because WebMD’s Terms and Conditions state “This Site Does Not Provide Medical Advice,” the website is not “legally obligated to provide a worst-case scenario” while most health professionals, at least in the United States, are held accountable if they do not provide patients with complete information regarding their health conditions.

Dr. Yuko, however, is most concerned with the use of health care sites as a substitute for obtaining diagnoses because people “can’t afford in-person care.” She stated, “This in itself is an ethics issue, but one from a societal, distributive justice perspective, highlighting the fact that not everyone has access to effective, affordable health care.”

Read the full article at GOOD.