Preimplantation genetic testing & hereditary cancer syndromes - research network meeting
Event details
Description
Dr Stefania Vicari and Dr Emily Ross (both Department of Sociological Studies) are hosting an interdisciplinary ‘think tank’ event on pre-implantation genetic testing (PGT) for hereditary cancer syndromes. This is in collaboration with iHuman, the university’s research institute for the study of the human. The session is part of a programme of events developed for the fifth theme of our cancer research strategy on enhancing patient experience and voice, co-led by Stefania and Dr Catriona Mayland.
During the session we will learn more about this procedure and the pathways experienced by patients. We will also discuss some of the social and ethical implications of this technique when applied to hereditary cancer syndromes such as BRCA 1/2 and Lynch Syndrome. There will be time for group discussion about what the widespread provision of such techniques means for understandings of cancer as a disease, and how these perspectives could be applied to anticipated future developments in new reproductive technologies. We will also think about the implications of PGT for understandings of IVF as a ‘routine’ technology within reproductive care, and how this may be refiguring meanings of infertility.
The event is aimed at those with an interest in (pre-)cancer patient experiences and quality of life, and new reproductive technologies - particularly those relating to prenatal diagnosis and disease or disability. We hope to bring together researchers from all disciplines across the university and clinical professionals, at all career stages. Confirmed speakers are Richard Sayers, genetic counsellor (ºù«Ӱҵ Children’s NHS Foundation Trust) and Emily Ross, Research Fellow (Department of Sociological Studies).
Refreshments and lunch will be provided. This meeting will be in person in The Wave.