January 28, 2009
A Short Stay in Switzerland is a BBC dramatisation telling the true story of Dr Anne Turner. Diagnosed with the degenerative neurological condition Progressive Supranuclear Palsy (PSP) and facing progressive deterioration in her condition, Dr Turner decided that she would end her own life by travelling to the Swiss clinic ‘Dignitas’. Unlike the UK, assisted euthanasia is legal in Switzerland. A Short Stay in Switzerland tells a highly emotive account of a woman who wishes to “die with dignity”, a decision eventually supported by her children.
A Short Stay In Switzerland - BBC 1 Sunday 25th January 2009, 21:00. The moment Dr Anne Turner tells her children that she has PSP.
The programme follows the events during the final stages of Anne Turner’s life. Although the dramatisation attempts to illustrate events as accurately as possible, it does so with a clear agenda in favour of her autonomous decision and it does not discuss the other possible alternatives when faced with such a situation in any detail.
There is, however, a section of the programme which shows Dr Turner’s children attempting to convince her that her life is worth living and that they can provide palliative care for her (00:25 :10 – 00:33:33). In this specific case, Dr Turner succeeds in her wish after an unsuccessful suicide attempt in her home persuades her children how determined she is. (Warning: if using the section indicated by the timings above, please be aware that the scenes that follow, graphically depict Turner’s earlier suicide attempt and therefore may not be suitable for all audiences).
There is also a BBC news article about the programme and you may be interested in this post on Panorama – I’ll die when I choose.
BBC News article 22nd January 2009. 'A Short Stay in Switzerland'.
A Short Stay in Switzerland was first broadcast on BBC 1 21:00 – 22:30 (90 minutes) Sunday 25th January 2009, and is available on BBC iPlayer until 10:29pm Sunday 1st February 2009.
January 26, 2009
Narrator Bill Paterson: "A child born in 1953, the structure of DNA has just been discovered. 1989 and this baby's genetic fingerprint can be identified. The first single gene for Huntington's disease has been discovered. 2003 this child's entire genetic code can now be read and faulty genes in his DNA can be adjusted. Another birth, but this time no ordinary miracle. The baby's sex and eye colour were decided before she was conceived; also her hair, the shape of her nose and her intelligence. The date of her birth? Perhaps only a few years from now. She's born from a revolution in genetics. A revolution where each new step brings new questions of ethics and responsibility. And as the promises of the science gets greater, so do the questions for all of us get bigger."
DNA – The Promise & The Price provides an excellent resource for discussing the ethical implications of advancing genetic research, focusing on; gene therapy, stem cells and cloning. The documentary examines the frontiers of genetic science, revealing how researchers attempt to fulfil DNA’s potential to help cure and prevent disease. It also questions how some aspects of these novel technologies may have significant consequences for individuals and society. Bill Paterson: “Much is promised by genetic science, the manipulation of our genes. But can it deliver? And if it does are we ready to take responsibility for meddling with the very fabric of life itself: our DNA”.
Professor Steve Jones: "When it comes to medical research, any medical technology that works, it is very quickly accepted by the public. Ethicists may not like it, scientists may not like it, but the public, if they believe it works they will accept it, and the legislation will always follow. Ethics has always followed science, it's never led it and I don't see any reason why genetics is going to be any different. Ethicists would love to tell geneticists what to do, but I'm afraid the geneticists are not going to listen."
The topics found in DNA – The Promise & The Price include: genetics; genetic diseases; gene therapy; transplantation; stem cells; and cloning can all be found in the UK National Curriculum. Please note all timings mentioned include advertisement breaks – (00:04:51 – 00:08:00, 00:25:31 – 00:28:40 and 00:46:50 – 00:50:00)
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January 22, 2009
Listen again via the BBC Radio 4's Today programme archive
This brief post concerns a short section of BBC Radio 4’s Today programme, broadcast on January 7th 2009. The clip itself is approximately 4.5 minutes long and features interviews with Professor Simon Baron-Cohen, of the Autism Research Centre, and Joy Delhanty, professor of human genetics at University College London, who prospectively discuss the ethical issues involved in prenatal testing for autism. It was broadcast alongside the corresponding edition of the BBC News’ weekly column Scrubbing Up, in which leading clinicians and experts give their perspectives on various issues in health and bioethics.
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January 21, 2009
Watch this episode via the BBC iPlayer (available until January 27th 2009)
The issue of resource allocation in the NHS has cropped up several times in recent programmes (see, for example, Dom’s on the Case regarding the “postcode lottery”. The present post examines the ethical issues implicit in a different aspect of resource allocation in healthcare: the potential for conflict between traditional medical ethics and core NHS values and increasingly prominent views of the individual as both responsible and accountable for their own health status. This tension came to the fore in Just, a recent episode of the BBC drama Holby City (first broadcast on BBC1 at 8.00pm on 20th January 2009), and is captured nicely in one particular quote from the programme in which surgeon Ric Griffin challenges his patient, an obese smoker, “if you can’t be bothered to look after yourself, then why should we?” (00:38:07)
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