In Fall 2022, conservative pundits condemned Senator-elect John Fetterman (D-PA), who had survived a stroke the previous spring, using discriminatory […]

In Fall 2022, conservative pundits condemned Senator-elect John Fetterman (D-PA), who had survived a stroke the previous spring, using discriminatory […]
In 2020, at the beginning of the pandemic, my friend and I were in the midst of writing our honors […]
When I was researching my first book, The Modern Period: Menstruation in Twentieth-Century America (2009), one of the most frequent […]
During one of my last visits with abortion activist Patricia Maginnis in 2015, she handed me The Abortion Handbook for […]
In 1929, a young woman entered Koch Hospital in St. Louis, Missouri. Her symptoms may have included coughing, difficulty breathing, […]
In 2018, Gerber made headlines for selecting baby Lucas as the winner of its Spokesbaby Contest, making Lucas the first […]
In May 2022, Irish social and mainstream media were alive with heated discussion of the terms of proposed agreements between […]
By Ginny Engholm
As everyone who reads this blog (or is on Facebook or Twitter) is by now well aware, the Supreme Court’s recent ruling in the Hobby Lobby case has dealt yet another powerful blow to women’s right to access contraceptives and manage their own health care, reproductive choices, and bodies. But a recent law—this one in Louisiana and regarding prenatal testing and counseling—poses yet another, but much less recognized, threat to women’s reproductive freedom. In May, Louisiana joined several other states (Massachusetts, Kentucky, Delaware, and Maryland) in passing a version of the Down Syndrome Information Act. This measure is part of the pro-information movement, which attempts to balance disparate groups and agendas within the Down syndrome community by bringing together both pro-choice and pro-life Down syndrome advocates in favor of providing women balanced, medically-accurate, and sensitive information about options when faced with a prenatal diagnosis of Down syndrome. The act as intended requires doctors to give appropriate medical information about the diagnosis and the options. It also requires doctors to give referrals to genetic counselors and relevant support services when delivering a prenatal diagnosis of Down syndrome to a patient.
By Mary Elene Wood
A highway patrol officer straddles a woman who lies on her back by the side of a highway. His arm lifts high into the air, then, with what looks like substantial force, he strikes her in the face with his clenched fist. He does this over and over again. Early in July, news programs around the country quickly spread the story of a California Highway Patrol officer caught on videotape violently beating Marlene Pinnock, a 51-year-old homeless, presumably mentally ill, woman, along the side of a freeway in Los Angeles. The California Highway Patrol claimed that the officer was only trying to stop the woman from walking out into traffic, yet journalists across the U.S. decried, in one writer’s words, “the lack of training given to law enforcement officers to handle such people, even though officers all too often are society’s frontline mental health care providers.”
By Sarah Handley Cousins
Several months ago, when I submitted my first blog post for Nursing Clio, I included a short section about Civil War veterans who had lost their right to a pension because they had deserted the army during the war. But after discussing it with our editors, I decided to remove the section – after all, we thought, desertion isn’t really a current issue, right? I was more than a little surprised when, a few months later, the topic of military desertion became headline news.
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