Promises, promises… We take it as a given that schooling is good for us, that overall population health increases with […]
Police Brutality, Mental Illness, and Race in the Age of Mass Incarceration
On November 9, 2014, two Ann Arbor police officers shot and killed Aura Rosser, a 40-year-old black woman, after responding […]
Pregnancy, Fear, and Conformity
Last fall, while in the midst of a severe head cold and four months pregnant, I emailed my obstetrician: “can […]
Come to the Dark Side: Disability as “Dark” Civil War History
By Sarah Handley-Cousins
While the rest of the world was happily decking the halls and calling for goodwill toward men, Civil War historians — in the now-famous words of Historista blogger and historian Megan Kate Nelson — were “freaking out.”
They weren’t freaking out because of the discovery of some great new source material, or an exciting new publication. They were freaking out because both Civil War History and The Journal of the Civil War Era, the two major journals in the field, each published an article in their December issues that criticized the state of current Civil War research and writing. The major concern for the articles’ authors — Gary Gallagher and Kathryn Shively Meier for JCWE and Earl J. Hess for CWH — was that Civil War military historians, already a dying breed, are being hurried to their demise by eager social and cultural historians who dismiss military history as unscholarly and old-fashioned. Earl Hess suggests that “understanding the real battlefield of 1861-1865 is essential to understanding everything else about the Civil War.”[1] Gallagher and Meier assert that “because the Civil War was a massive war, every scholar of the conflict should be at least basically versed in its military history.”[2]
Prenatal Testing and Counseling: The New Front of the Abortion Wars?
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.
On the Verge of a Nervous Breakthrough?: Interpreting Mental Illness
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.”
Adventures in the Archives: Searching for the Past
by Sarah Handley-Cousins
For much of this past year, I’ve been entrenched in dissertation research. Despite the long hours hunched over dusty papers, trying to decipher century-old handwriting, generally while cold and hungry, I’m not complaining. I’m continually amazed that I’m getting the opportunity to do exactly what I’ve always wanted: the work of history. What I wasn’t prepared for, necessarily, was the emotional work that would come along with it.
The Paralympics, Past and Present
I probably don’t need to tell you that the 2014 Winter Olympics captured the attention of millions of people in the […]
Eugenics and Genetics in the News in 2013
By Tina M. Kibbe
Happy New Year! As another year ends, I wanted to take a look at three news stories involving eugenics and genetics in 2013 that you may have missed.
Sex and Disability, Part 2
By Adam Turner
This is the second post in a two-part reflection on some of the issues raised by a September BBC news story, Judge Approves Man’s Sterilisation in Legal First. (See part one for a synopsis of the story.) In part one I listed three reasons why people often believe adults with intellectual and developmental disabilities (I/DD) should not have sex or sometimes even be in romantic relationships. I discussed number one in part one, and will now look at numbers two and three.
