Since 1945, no German book on eugenics has been published. However, during two decades of reconstruction of the science of human genetics, which is fundamental to eugenics, the problems of eugenics repeatedly came to the fore and were discussed lively in wide circles.
In the preface to his monograph Eugenik. Kommende Generationen in der Sicht der Genetik (1966, Eugenics: Coming Generations in the View of Genetics), the West German human geneticist Otmar von Verschuer (1896–1969), presenting himself as an expert in eugenics, emphasized that it was necessary for “this complex of topics” to be presented in a way that was “generally understandable.” His academic accomplishments might have proven his expertise as his career was largely intertwined with the academic boom in eugenics, or “racial hygiene,” as it was called in Germany before 1945. With the help of hereditary knowledge, the eugenics movement aimed to improve the genetic health of human populations. In addition to their intention to solve social problems by biological means, eugenicists also desired to be perceived as a scientific community. In the Weimar Republic, representatives of racial hygiene not only gained access to political decision-makers but also began an intensive process of professionalization.
Continue reading “Human Genetics with(out) Eugenic Knowledge? Towards a History of Knowledge about Human Heredity in West Germany”
We are all historians of the present. At least we should be. Many fellow historians of knowledge are currently using a wide variety of media to share their experience and research in an effort to put the global response to the COVID-19 pandemic into context. Twitter is one medium where this conversation is especially lively, as Eileen Sperry has noted on Nursing Clio, a wonderful group blog that is also active on Twitter. One can find these parts of Twitter by searching for the relevant hashtags, for example, #histmed (history of medicine) and the much more generic #twitterstorians (historians on twitter).
Continue reading “Viral Hive Knowledge: Twitter, Historians, and Coronavirus/COVID-19”
Washington, DC, Sept. 6-7, 2019
Application deadine: Dec. 15, 2018
When the French pharmaceutical company Roussell Uclaff, a subsidiary of the German chemical giant Hoechst AG, was ready to introduce an abortion pill in 1988, American activists flooded the company’s headquarters near Frankfurt with protest letters. In response, the company’s German CEO mandated to stop the project. But the French state, a Hoechst minority shareholder, took the idea across the border, patented it, and embarked on medical trials for the new product in France. Ten years later, scientists in the United States successfully isolated human embryonic stem cells. The country’s regulatory framework had left them free to let the cells proliferate indefinitely. But researchers adopted concepts implemented in Britain to limit the cells’ growth to 13 days after gestation.
In the 1850s, a physician at St. Bartholomew Hospital in London struggling with an unclear case of fever with affection of the bowels might have wanted to find information about the patient’s prognosis or an alternative medical treatment. Likewise, a medical student preparing a case for presentation to the hospital society, might have wanted further information about typhus fever, namely, its course, average prognosis, possible complications, and treatment. Both doctor and student would probably visit the library of the hospital’s “Medical College” to find comparable cases and case reports in voluminous bound casebooks.
Continue reading “Medical Knowledge and the Manual Production of Casebook-Based Handbooks”
Over four decades ago, the distinguished epidemiological psychiatrist Norman Sartorius wrote, “the history of psychiatric classification is in fact a history of psychiatry.” During the 1960s and 1970s, Sartorius had been at the center of research by the World Health Organization (WHO) on the international classification and prevalence of mental disorders. During that era, the organization significantly transformed its classificatory manual, the International Statistical Classification of Diseases and Related Health Problems (ICD), releasing the ICD–9 in 1977. The ICD is the standard international manual for recording mortality and morbidity data for insurance and epidemiological purposes. WHO is currently in the final stages of completing its latest update to the text, ICD–11.
Continue reading “Mental Disorders, Collective Observation, and the International Classification of Diseases”