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June 16, 2011

by Jennifer Lahl
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side bar side bar side bar side bar side bar A landmark victory has just been won in Pratten v. British Columbia, a case that will undoubtedly set a significant legal precedence. On May 19, the Supreme Court of British Columbia ruled against the practice of anonymous sperm (and egg) donation, instead arguing in favor of donor-conceived children and their right to have access to information about their biological parents. The court's decision stems, at least in part, from the notion that, when it comes to children, biology and biological parents do, in fact, matter.

Olivia Pratten, a brave young woman from Toronto, was at the heart of this legal battle. At the age of five, Olivia's parents told her that she was conceived using an anonymous sperm donor, and thus, that the man she called "dad" was not, in fact, her biological father. And as with many children created through anonymous sperm and egg donation, she had a lot of questions: Who was her biological father? What did he look like? What similarities did she share with this man? But because Olivia's biological father donated his sperm anonymously, most of her questions had no answers.

When Olivia turned nineteen, she visited the doctor who had inseminated her mother. But because the donor was anonymous, the doctor was only able to disclose a few facts about him: he was Caucasian and had blue eyes and brown hair. While this information did help to define a previously unknown figure for Olivia, ultimately, it was too vague to be of any real use in her search for her biological father. And the doctor had shredded all the medical records from the insemination, leaving no trail for Olivia to find her biological father.

Much like Barry Stevens, who is also a product of anonymous sperm donation and producer of two documentary films on the subject (Offspring and BioDad), Olivia experienced "genealogical bewilderment." Barry borrows this phrase from psychologist H.J. Sants in an attempt to acknowledge and describe the feelings of people like Olivia and himself who have little or no information about one or both of their natural parents.

Olivia, Barry (who estimates that he has over 100 half-siblings), and thousands of others have a deep longing to know who they belong to, where they come from, and who they look like. They also rightly argue the need to know their medical history, which is passed to them, in part, through their biological parents. But they have been denied answers to these most basic questions. Not so in British Columbia anymore, thanks to Olivia's case, where she sought to right this wrong, ensuring that records are maintained and information is openly available to offspring. In the wake of this decision, the court has given the province fifteen months to write a new adoption law that will recognize the rights of donor-conceived people to access this information about their biological parents.

Most of us have grown up in an era of open-adoption, a necessity in the age of genetic medicine, and these children have access to their biological information. Given this, many might wonder why this practice hasn't been extended to donor-conceived children. Objections to the ruling in Canada have already been expressed loud and clear, mainly from the fertility industry itself. Sean Tipton of the American Society of Reproductive Medicine stated that the organization will strongly oppose any move to ban anonymous gamete donations in the U.S. because "We think people ought to be able to build their families the way they see fit…and we don't want to change the rules in the middle of the game." Those in the industry argue that donations will dry up if anonymity isn't protected, and that protections need to be put into place to protect donors from children finding them and wanting money, or to be welcomed and added into their families.

Fortunately, brave people like Olivia Pratten are making their voices, their needs, and their rights known, and the courts are changing the game. Sorry, Dr. Tipton, it is not just about parents creating the families that they want; it's also about these children and what they want, need, and have a right to know. And Olivia and other donor-conceived children have a right to satisfy their most basic human need for identity, which is intricately connected to their biological parents.

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left links right
Ruling gives birth to rights for donor-conceived tots
Bio-Dad - Documentary (Barry Stevens)
Offspring - Documenary (Barry Stevens)
The Rights of Sperm Donor Dads
Are Dads Disposable?
The essential public purpose of marriage
 
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We live complex lives. We strive to sort out priorities that sometimes conflict or seem incompatible. A moral framework is needed to help us understand the reality around us. Our Judeo-Christian heritage provides a framework to help us comprehend the choices we make and the conflicts that arise over them. It is not only the main source of our spiritual values, but also many of the secular values we depend on.

tothesource is a forum for integrating thinking and action within a moral framework that takes into account our contemporary situation. We will report the insights of cultural experts to the specific issues we face believing these sources will embolden people to greater faith and action.
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  Jennifer Lahl
Jennifer Lahl, is founder and national director of The Center for Bioethics and Culture Network, an organization working to shed light on the bioethics issues within our culture that most profoundly affect our humanity, and advancing the voice of a morally responsible science that respects the inherent value of humanity and that celebrates its beauty and complexity. Lahl couples her 25 years experience as a pediatric critical care nurse, hospital administrator and senior-level nursing management, with a deep passion to speak for those who have no voice. Lahl's writings have appeared in various publications including the San Francisco Chronicle, the Dallas Morning News and the American Journal of Bioethics. As a field expert she is routinely interviewed on radio and television including ABC, CBC, PBS and NPR and called upon to speak alongside lawmakers and members of the scientific community, even being invited to speak to members of the European Parliament in Brussels to address egg trafficking. She is founding director of Every Woman First and serves on the North American Editorial Board for Ethics and Medicine as well as Board of Reference for Joni Eareckson Tada's Institute on Disability.
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