scholarly journals Don Lindberg’s outreach legacy at the National Library of Medicine

2021 ◽  
pp. 1-9
Author(s):  
Elliot R. Siegel

Friends and colleagues of Donald A.B. Lindberg M.D. came together to give tribute to his extraordinary contributions during his tenure (1984–2015) as Director of the U.S. National Library of Medicine (NLM). Dr. Lindberg died in 2019. The book, Transforming biomedical informatics and health information access: Don Lindberg and the U.S. National Library of Medicine. includes four sections. The ten edited chapters in section three (the Outreach section) are briefly summarized in this overview. As Associate Director for Health Information Programs Development, Elliot R. Siegel Ph.D. coordinated NLM’s outreach programming under Dr. Lindberg’s leadership from its inception in 1989 to his own retirement in 2010. Dr. Lindberg’s legacy at NLM is one of new possibilities imagined, significant changes made in the mission and ethos of a venerable institution, and numerous successes achieved in a variety of settings and contexts. Like so much else Dr. Lindberg accomplished, these Outreach programs that profoundly changed the character of NLM would likely not have occurred without him. He made a difference.

2020 ◽  
Vol 47 (2) ◽  
pp. 236-253
Author(s):  
Wu Huiyi ◽  
Zheng Cheng

The Beitang Collection, heritage of a seventeenth- and eighteenth-century Jesuit library in Beijing now housed in the National Library of China, contains an incomplete copy of Pietro Andrea Mattioli’s commentary on an Italian edition of Pedanius Dioscorides's De materia medica (1568) bearing extensive annotations in Chinese. Two hundred odd plant and animal names in a northern Chinese patois were recorded alongside illustrations, creating a rare record of seventeenth-century Chinese folk knowledge and of Sino-Western interaction in the field of natural history. Based on close analysis of the annotations and other contemporary sources, we argue that the annotations were probably made in Beijing by one or more Chinese low-level literati and Jesuit missionaries during the first two decades of the seventeenth century. We also conclude that the annotations were most likely directed at a Chinese audience, to whom the Jesuits intended to illustrate European craftsmanship using Mattioli’s images. This document probably constitutes the earliest known evidence of Jesuits' attempts at transmitting the art of European natural history drawings to China.


1948 ◽  
Vol 1 (01) ◽  
pp. 69-75
Author(s):  
R. B. Michell

At the first International Meeting on Radio-Aids to Marine Navigation held in London in May 1946 some 105 delegates of twenty-three maritime nations met to discuss and witness demonstrations of some of the remarkable advances made in radio-navigation during the war and to consider the progress made in relation to their peacetime uses for marine transport.At the invitation of the U.S. government a second meeting was held a year later, in New York and New London, to show the progress made in America, to illustrate, with demonstrations, the U.S. policy and to pave the way to international standardisation. The U.K. delegation was led by Sir Robert Watson-Watt.


2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Per Egil Kummervold ◽  
Rolf Wynn

The aim of this study was to summarize and analyse findings from four prior studies on the use of the Internet as a source of health information in five European countries (Norway, Denmark, Germany, Greece, and Portugal). A cross-study comparison of data was performed. All the studies included fit with a trend of a sharp and continuous growth in the use of the Internet for health information access in the major part of the last decade. Importantly, the Internet has become an important mass media source of health information in northern Europe. While the use of the Internet for health information is somewhat less common in the south European countries, its use is also clearly increasing there. We discuss the advantages of cross-study comparisons of data and methodological challenges. As the use of the Internet for health information is likely to peak in some countries in the near future, new population surveys on health information access should focus more on the details of information that is accessed and which sites that are most used and trusted.


2016 ◽  
Vol 22 (4) ◽  
pp. 992-1016 ◽  
Author(s):  
Martina A Clarke ◽  
Joi L Moore ◽  
Linsey M Steege ◽  
Richelle J Koopman ◽  
Jeffery L Belden ◽  
...  

To synthesize findings from previous studies assessing information needs of primary care patients on the Internet and other information sources in a primary care setting. A systematic review of studies was conducted with a comprehensive search in multiple databases including OVID MEDLINE, CINAHL, and Scopus. The most common information needs among patients were information about an illness or medical condition and treatment methods, while the most common information sources were the Internet and patients’ physicians. Overall, patients tend to prefer the Internet for the ease of access to information, while they trust their physicians more for their clinical expertise and experience. Barriers to information access via the Internet include the following: socio-demographic variables such as age, ethnicity, income, education, and occupation; information search skills; and reliability of health information. Conclusion: Further research is warranted to assess how to create accurate and reliable health information sources for both Internet and non-Internet users.


2020 ◽  
Vol 2 (4) ◽  
pp. p14
Author(s):  
Mingming Zhuang

Although transnational surrogacy has received much criticism owing to racial and class issues, the U.S. media portrays domestic surrogacy with overwhelming positive languages by employing specific narrative frameworks. Accompanying this shift, it is not so surprising that the number of gestational carrier cycles have skyrocketed from 727 to 3,423 over the last decade. (Note 1) In particular, increase in the number of gay and single men looking for surrogacy has yielded more controversies. This paper asks the following questions: How does the documentary Made in Boise present surrogacy in the context of a broader debate over feminist and LGBT’s positions? How are gay parents used in the altruism narrative framework to downplay exploitation of surrogacy? By providing insight into the intricate economic and power relationships between surrogate and a new emerging group of intended parents, my case study prompts broader questions such as: How to best document the most authentic narratives of the surrogates? How can feminist and LGBT scholars reconcile their viewpoints over surrogacy? These are pertinent questions concerning exploitation and coercion in the industry, thus influencing future feminists’ studies on reproductive technology and politics.


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