Category: 2015

2015, Multimedia + Performance

Welcome to 23andMe

OLJA BUSBAHER

Olja analyzes the marketing strategy of genomic sequencing company, 23andMe, to understand the role of rhetoric in explaining (or failing to explain) the potential risks and benefits of undergoing personal genome sequencing. Olja deconstructs the 23andMe starter kit, carefully dissecting the implications of 23andMe’s privacy statement.

 

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2015, Multimedia + Performance

geno(ME)

LENA BICHELL

Lena explores the relationship between every individual’s unique genetic code and the quest for greater knowledge of the collective human genome. Lena offers an interactive art piece that allows participants to build their own simplified DNA double helix, and then challenges participants to “donate” their unique genome to the larger effort toward understanding genomics on a broader scale.

 

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2015, Multimedia + Performance

Dilemma

VALERIA BALZA

Valeria presents five photographs that underscore the tension between the potential risks and benefits of personal genomic sequencing. Valeria’s work illuminates the dilemmic nature of undergoing genomic sequencing, as individuals must consider the implications of their genetic results.

 

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2015, Multimedia + Performance

“Liberty and Justice for All”: A Reflection

MARNIE KLEIN

Marnie Klein (NHS’18) first encountered the now-infamous Guatemala STD Experiments (1946-1948) in a class on bioethics with KIE Scholar Tom Beauchamp. American physicians intentionally infected a variety of vulnerable populations — prisoners, mental patients, prostitutes, orphans, school children — with sexually transmitted diseases without informed consent.

Klein explains, “While many subjects were treated with antibiotics, many were not, resulting in at least eighty deaths and countless infections both inside the study and in the larger population.”

Her multimedia piece vividly evokes the experiences of four victims of these experiments: a sex worker, a prisoner, an orphaned child, and a soldier, whose differing backgrounds raise intersecting and divergent moral dimensions of the case.

“Art allows us to talk about things that otherwise make us uncomfortable,” says Klein, “[making] bioethics tangible through stories.”

2015 FIRST PRIZE WINNER

 

2015, Poster Presentation

Ethical Considerations of the Medicalization of Female Genital Mutilation/Cutting

MARGARET DUNNE + ELEANOR BIRCH

Margaret Dunne (NHS’17) and Eleanor Birch (NHS’17), both International Health majors, first encountered the issue of Female Genital Mutilation/Cutting (FGM/C) — the non-medical partial or total removal of the external female genitalia or other injury to female genital organs — in a class at Georgetown on Maternal and Child Health.

Most FGM/C is performed by “traditional circumcisers,” but nearly one-fifth is performed by healthcare professionals in a practice known as “medicalized” FGM/C. The poster focuses on the moral responsibility of physicians and others involved in the practice, suggesting that there are no easy or quick answers in this domain.

Though both authors began their exploration firmly opposed to the medicalization of the practice, their research ultimately led them to reverse course, and their poster advocates medicalization as a harm-reduction technique and morally-acceptable intermediate step to the ultimate eradication of the practice.

2015 FIRST PRIZE WINNER

2015, Policy Proposal + Business Plan

Influenza Vaccination for Healthcare Workers

ANDREW MESHNICK

Andrew proposes legislation to use federal funds to mandate an influenza vaccine for healthcare workers, with an exception for those who cannot receive the vaccine for medical reasons. Andrew draws upon the duty of healthcare providers to do no harm to their patients to advocate for the mandate on flu vaccines while weighing the potential conflict of individual healthcare providers’ autonomy.

2015, Policy Proposal + Business Plan

The Kidney Donation Compensation and Coordination Act

ROSA CUPPARI

Rosa promotes the implementation of the Spanish model of organ donation to address the kidney donation shortage in the United States. Rosa suggests that this model, which actively recruits potential donors and counsels the families of brain-dead or recently deceased patients, will increase the number of lives saved, reduce healthcare costs, and significantly diminish the length of the kidney transplant waitlist.