Thursday 24 September 2009


Since 1971 DES exposed Australians have borne the brunt of the negative consequences of failures to report the side effect cancer due to DES. Without having these failures to report cases, it would enable a more accurate estimation of the magnitude of the Australian DES problem and hence, greater validity and recognition to the DES issue.

From 1983 to 2001 the number of DES associated cancer cases held in data by our drug watchdog, the Therapeutic Goods Administration (TGA) strangely remained static at 4 cases, whilst the figures elsewhere in the world were on a slow rise. Media reports during this period consistently cited 10 cases, sourced from the Royal Australian and New Zealand College of Obstetricians and Gynaecologists.

The TGA’s Drug Safety and Evaluation Branch explanation for the static figure of 4 cases (letter 29/3/01) to DES Action Australia-NSW was that “1983 was the end of the period” for identifying cases. It was explained that specialist centres within Australia were maintaining registers and that these centres chose not to report to the Adverse Drug Reactions Advisory Committee (ADRAC). Adverse Drug Reaction Unit correspondence (31/5/01) explains the ADRAC received a phone call by an un-named doctor stating specialist clinics had been set up and that reporting to the ADRAC was not seen as necessary.

In fact, there were NO such specialist centres within Australia maintaining registers. The number of women diagnosed from 1983-2001 who would otherwise have been reported, remains a mystery.

Minutes of the Australian Drug Evaluation Committee acquired by DES Action Australia-NSW reveal the following:

  • One doctor on the committee had two patients with DES associated cancer, neither of which were reported and one of whom died.

  • The Congenital Abnormality Sub Committee believed there were 4 or 5 cases of the cancer type associated with DES in children in Sydney that had not been reported nor investigated. In later meeting this figure is said to be at least 5 children.

[Note: Prior to the DES problem this cancer type only occurred in older women.]

  • The Department of Obstetrics & Gynaecology, University NSW was said to have record of 5 cases of DES associated cancer that had not been reported.

The TGA has only ever conducted one cross-check of its data (2004) with those Australian cases listed on International DES Cancer Registry held in Chicago, USA

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TGA refusal to conduct further checks was on grounds that it is not their administrative role to act as a registry.

On another matter, the ADRAC was unable to afford an explanation to DES Action Australia-NSW for their 10 year delay in entering the data of a 4 year old girl diagnosed in 1972.

The following is an excerpt in correspondence from Senator the Hon Jan McLucas 16/2/09:

“The TGA published the information in April 2008 to assist in informing women who have been exposed to DES about the need to undergo regular screening for cervical and breast cancer. The TGA advised the Department that DES is not a therapeutic good currently on the Australian Register of Therapeutic Goods and is not currently available via any avenue of supply in Australia. As such, it is not the role of the TGA to provide information about DES or to promote public health messages to DES exposed women.”

In spite of continuing to receive reports of DES associated cancer since the withdrawal of DES from the Australian Register of Therapeutic Goods (ARTG), the TGA now has no role in issuing warnings about DES, but it appears it can decide to do so “to be helpful”. This has enormous ramifications for all victims of dangerous drugs that have been withdrawn from market and which, as a consequence are removed from the ARTG, since it may preclude affected individuals from further information that may be potentially life-saving. Adding insult to injury, the Department of Health and Ageing may then choose not to properly support these individuals with information. Lack of support by the Department of Health and Ageing in appropriately informing people about DES has been our experience.

Wednesday 23 September 2009

Finding Out About DES By Chance?

Since 2004 DES Action Australia-NSW has organised DES Awareness Weeks June 1-7 on the NSW Health Calendar. These events have only been possible with the practical and financial assistance of members and associates. With numerous media articles about DES published nationally, the response from many DES exposed people who chance upon these articles has been absolute anger and distress. This has been as a consequence of NOT having been directly informed of the dangers of DES previously via government public health programs. For these individuals their health, and indeed, possibly their lives have unnecessarily been jeopardised through not knowing their special cancer preventive health care.

For many people, finding out about DES is like finding the last piece of a puzzle in their health problems. This is especially so, when they are the only sibling in their family exposed to DES and are alone experiencing many of tell-tale signs of DES exposure, eg, recurrent miscarriages, ectopic pregnancies.

One woman reported to us having been diagnosed with the DES associated cancer type at a young age in the 1980s and had NEVER been asked by any health care provider about the possibility of her exposure. Stories along these lines are never ending to us year after year.

Finding out about DES by chance is NOT good enough! Many voices need to be heard in the face of government opinion that “DES information could create unnecessary anxieties for women who may not know if they have been DES exposed.”

You can help change this horrendous situation for DES exposed Australians by writing to:

The Hon Nicola Roxon MP, Minister for Health and Ageing, MG 50, Parliament House, Canberra ACT 2600 Email:


The Hon Peter Dutton MP, Shadow Minister for Health and Ageing, House of Representatives, Parliament House, Canberra ACT 2600 Email:

Let these politicians know that people need to be directly informed about DES in public health programs and certainly let them know your circumstance if you only found out about DES by chance.

Bell's Book

DES Daughters, Embodied Knowledge, and the Transformation of Women's Health Politics in the Late Twentieth Century

ISBN: 9781592139194

In DES Daughters, Susan Bell recounts the experiences of this generation of “victims.” In moving, heartfelt narratives, she presents the voices of those women who developed cancer, those who were cancer-free but have concerns about becoming pregnant, and those who suffered other medical and/or reproductive difficulties.

Bell examines the hierarchy of knowledge and power of scientists, doctors, and daughters, tracing the emergence of a feminist health movement. The “embodied knowledge” of these DES daughters prompted them to become advocates and form a social movement that challenged reproductive medical knowledge specifically, but also the politics of women’s health in general. Bell’s important book chronicles the history and future of these grassroots activists born out of illness, suffering, and uncertainty.