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UK Judge Rules Teen With Rare Disease Lacks Mental Competence to Pursue Experimental Treatment

by Kaia

In a somber legal decision, a 19-year-old woman in the United Kingdom, afflicted with a rare and debilitating disease, has been deemed incompetent to make decisions regarding her medical treatment. The ruling has raised concerns about the potential withdrawal of treatment, in accordance with her healthcare providers’ recommendations.

The young woman, identified only as “ST” for legal reasons, is grappling with a progressively degenerative mitochondrial disorder that has left her facing a grim prognosis, as reported by The Telegraph. Desiring to explore experimental treatment options abroad, ST’s hopes were met with a judicial ruling that determined her incapacity to make autonomous decisions regarding her healthcare.

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Medical experts overseeing her care contend that she is either currently in, or will soon enter, the final stages of her life, characterized as “actively dying.” In light of this, the National Health Service (NHS) trust overseeing her case has petitioned the court to authorize a palliative care plan that includes the discontinuation of dialysis, which would inevitably lead to her passing due to kidney failure within a matter of days.

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The family of the young woman has expressed their objection to the ruling regarding her alleged incapacity, and they have cited various legal constraints impeding their ability to garner public support for her cause. This case has ignited a poignant debate surrounding the intersection of patient autonomy, medical ethics, and end-of-life care decisions within the UK’s legal framework.

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