Institution/Affiliation
Cedarville University
Keywords
Autonomy, beneficence, minor, disability
Abstract
On June 14, 2016, 5-year old Julianna Snow died at home, in accordance with her stated wishes not to return to the hospital. Julianna suffered from a severe form of Charcot-Marie-Tooth disease, an inherited neurodegenerative disorder which, while not always lethal,1 had weakened her body to the extent that even a cold could be fatal.
Julianna’s case raises important questions about patient autonomy and end-of-life care for children. The child did not wish to return to the hospital, and was willing to go to heaven instead.6 Though her parents respected her autonomy and honored her decision, the question remains: did Julianna have the decision-making capacity to make a life-or-death decision at such a young age? Are there cases where autonomy may have to be sacrificed in favor of other important ethical determinants, such as beneficence or non-maleficence?
Article Number
2
DOI
10.15385/jbfp.2017.3.1.2
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
Recommended Citation
Kuruvilla, Heather G.
(2017)
"Autonomy and Patient Care: To What Extent Should Children Make Their Own Decisions?,"
Bioethics in Faith and Practice: Vol. 3:
No.
1, Article 2.
DOI: 10.15385/jbfp.2017.3.1.2
Available at:
https://digitalcommons.cedarville.edu/bioethics_in_faith_and_practice/vol3/iss1/2
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