TY - JOUR
T1 - Donor conception legislation in Victoria, Australia: the "Time to Tell" campaign, donor-linking and implications for clinical practice
AU - Johnson, Louise
AU - Bourne, Kate
AU - Hammarberg, Karin
PY - 2012
Y1 - 2012
N2 - The State of Victoria in Australia was one of the first jurisdictions in the world
to introduce legislation regulating donor conception. Under the Infertility
(Medical Procedures) Act 1984 (Vic), donor-conceived people, aged 18 years
and over, parents of children under 18 years, and donors gained the right to
apply for the release of identifying information about each other recorded in a
Central Register. As a result, of this and subsequent legislation, services
providing donor treatment were obliged to change clinical practice relating to
recruitment of donors, counselling of donors and recipients and record-
keeping. Since this legislation was introduced in 1988, over 5,000 donor-
conceived children have been born and in 2006 the first 100 of these children
reached the age of 18. The Victorian Infertility Treatment Authority (ITA)
conducted a public education campaign to provide information and support to
people affected by the legislation. This article describes clinical practice
changes prompted by legislation, the ?Time to Tell? campaign and the service
model developed for linking parties on the donor registers. The Victorian
experience demonstrates that laws allowing the parties involved in donor
conception access to information about each other must be accompanied by
changes to clinical practice, public education about the implications of the
laws, and services to meet the needs of those seeking information relating to
donor conception and those contacted as a result.
AB - The State of Victoria in Australia was one of the first jurisdictions in the world
to introduce legislation regulating donor conception. Under the Infertility
(Medical Procedures) Act 1984 (Vic), donor-conceived people, aged 18 years
and over, parents of children under 18 years, and donors gained the right to
apply for the release of identifying information about each other recorded in a
Central Register. As a result, of this and subsequent legislation, services
providing donor treatment were obliged to change clinical practice relating to
recruitment of donors, counselling of donors and recipients and record-
keeping. Since this legislation was introduced in 1988, over 5,000 donor-
conceived children have been born and in 2006 the first 100 of these children
reached the age of 18. The Victorian Infertility Treatment Authority (ITA)
conducted a public education campaign to provide information and support to
people affected by the legislation. This article describes clinical practice
changes prompted by legislation, the ?Time to Tell? campaign and the service
model developed for linking parties on the donor registers. The Victorian
experience demonstrates that laws allowing the parties involved in donor
conception access to information about each other must be accompanied by
changes to clinical practice, public education about the implications of the
laws, and services to meet the needs of those seeking information relating to
donor conception and those contacted as a result.
UR - http://www.westlaw.com.au.ezproxy.lib.monash.edu.au/maf/wlau/app/document?&src=search&docguid=I4360d947b02311e18eefa443f89988a0&epos=7&snippets=true&f
M3 - Article
SN - 1320-159X
VL - 19
SP - 803
EP - 819
JO - Journal of Law and Medicine
JF - Journal of Law and Medicine
IS - 4
ER -