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1.
J Med Ethics ; 48(3): 200-201, 2022 Mar.
Article in English | MEDLINE | ID: mdl-34103366

ABSTRACT

In, 'Forever young: the ethics of ongoing puberty suppression (OPS) for non-binary adults,' Notini et al discuss the risks, harms and benefits of treating non-binary patients via identity-affirming OPS. Notini et al's article makes a strong case for OPS's permissibility, and their conclusion will not be disputed here. Instead, I directly focus on issues that their article addressed only indirectly. This article will use a hypothetical case study to show that while Notini et al's ethical conclusion might be spot on, that perhaps the method they took to get there was superfluous. If the medical community is to take LGBT testimony seriously (as they should) then it is no longer the job of physicians to do their own weighing of the costs and benefits of transition-related care. Assuming the patient is informed and competent, then only the patient can make this assessment, because only the patient has access to the true weight of transition-related benefits. Moreover, taking LGBT patient testimony seriously also means that parents should lose veto power over most transition-related paediatric care.


Subject(s)
Sexual and Gender Minorities , Trust , Adult , Child , Humans , Informed Consent , Morals , Parents , Puberty
4.
Am J Bioeth ; 19(2): 45-59, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30784385

ABSTRACT

In this article, I argue that (1) transgender adolescents should have the legal right to access puberty-blocking treatment (PBT) without parental approval, and (2) the state has a role to play in publicizing information about gender dysphoria. Not only are transgender children harmed psychologically and physically via lack of access to PBT, but PBT is the established standard of care. Given that we generally think that parental authority should not go so far as to (1) severally and permanently harm a child and (2) prevent a child from access to standard physical care, then it follows that parental authority should not encompass denying gender-dysphoric children access to PBT. Moreover, transgender children without supportive parents cannot be helped without access to health care clinics and counseling to facilitate the transition. Hence there is an additional duty of the state to help facilitate sharing this information with vulnerable teens.


Subject(s)
Adolescent Health/ethics , Ethics, Clinical , Gender Dysphoria/psychology , Health Knowledge, Attitudes, Practice , Human Rights , Parents/education , Transgender Persons/psychology , Adolescent , Bioethical Issues , Child , Female , Gender Dysphoria/drug therapy , Gonadotropin-Releasing Hormone/agonists , Humans , Male , Parents/psychology , Personal Autonomy
5.
HEC Forum ; 30(3): 297-318, 2018 Sep.
Article in English | MEDLINE | ID: mdl-30006852

ABSTRACT

In this paper, I aim to demonstrate that the consequences of the current United States health insurance scheme on both physician and patient autonomy is dire. So dire, in fact, that the only moral solution is something other than what we have now. The United States healthcare system faces much criticism at present. But my focus is particular: I am interested in the ways in which insurance interferes with physician and patient autonomy. (I do not consider The Affordable Care Act much of a change in this aspect of the system, for it still relies heavily on private insurance, albeit often subsidized.) I will argue in favor of an expansion of the traditional conception of what I call "medical autonomy" or "healthcare autonomy" and the usual role it plays in bioethical discussions. More generally, I show that in morally designing or evaluating any healthcare system, serious attention should be paid to how this system helps foster what I call active autonomy.


Subject(s)
Choice Behavior , Professional Autonomy , Bioethics/trends , Humans , Insurance Coverage/ethics , Insurance Coverage/standards , Quality of Health Care/standards , Quality of Health Care/trends , United States
6.
Hastings Cent Rep ; 48(4): 31-41, 2018 Jul.
Article in English | MEDLINE | ID: mdl-35227031

ABSTRACT

In 2010, a South Carolina mother was taken to court when her fourteen-year-old son reached 555 pounds. An article on the story reported, "His mother, Jerri Gray, lost custody of her son and is being charged with criminal neglect. Gray is facing 15 years on two felony counts, the first U.S. felony case involving childhood obesity." If the caretakers of obese children are negligent, then they are also morally and legally blameworthy. I want to suggest, however, that important ethical differences exist between negligent or abusive caretakers and the caretakers of obese children and that these differences ought to make a moral and legal difference. The distinctions are nuanced, and the ethical pictures in cases of abuse, neglect, and obesity are far from black and white. However, the various types of harm that children face from their caretakers should be placed in neither the same ethical nor the same legal category. When children are beaten or sexually molested, the justification for taking them out of the home is clear: the caretakers are violating the rights of their children. Similarly, with neglect, caretakers are failing to provide their children the necessities to which they are entitled. The central question that I want to address in this article is whether the actions (or inaction) of caretakers that allow a child to become obese are morally or practically analogous to physical abuse or neglect. Ultimately, I will argue that parenting that allows a child to become obese is so morally different from both abuse and neglect that it is best understood as falling outside these categories altogether. This conclusion has important moral, practical, and legal implications.

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