
Far from the Tree
2019

Representation Score
Good
2016
Director
Clare Richards
Runtime
59 minutes
Average Rating
No ratings yetNew Showbiz Analysis
This documentary serves as a powerful critique of medical authority and biological essentialism. By centering the lived experiences of the neurodivergent community, it shifts the conversation from clinical data to human rights and systemic ethics. The film treats people with Down’s syndrome as active participants in societal debates, disrupting traditional hierarchies and providing a platform for those most affected by screening policies. While the film excels in disability representation and cultural critique, it lacks specific information regarding racial diversity or LGBTQ+ narratives. This leaves certain demographic dimensions of the conversation unaddressed.
Category Breakdown
The documentary focuses on neurodiversity and reproductive ethics without addressing LGBTQ+ identities or narratives. There are no explicit mentions of LGBTQ+ characters or stories.
Sally Phillips leads the investigation, providing a strong female perspective on medical ethics. The film centers a maternal voice to challenge traditional healthcare hierarchies.
The provided information does not specify the racial or ethnic composition of the participants. Therefore, the demographic breakdown of the cast and experts remains unknown.
The film engages with progressive ethical frameworks by critiquing normative biological standards. It challenges the utilitarian drive for perfected populations through a lens of moral relativism.
Disability is central to this work. It involves individuals with Down’s syndrome directly in high-level ethical debates, granting them a significant role in driving the story.
Present on Screen
Limited or Absent
Official Synopsis
Documentary about Down's syndrome and the ethics of pregnancy screening, fronted by Sally Phillips. This film explores the science and thinking around the proposed new screening test for Down's syndrome and its possible availability on the NHS. Driven by the experience of raising her son Olly, who has Down's syndrome, Sally explores some of the ethical implications of our national screening policy. By talking to experts in the Down's syndrome community, the world's top scientists and including people with Down's syndrome in the debate, Sally investigates a thorny subject that begs questions relevant to us all: what sort of world do we want to live in and who do we want in it?

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