In 1866, a young man in Crestline, Ohio, visited Dr. J. Stolz to ask the physician for help. Mr. B’s […]
I’m Not Crazy!: Abby Norman’s Ask Me About My Uterus: A Quest to Make Doctors Believe in Women’s Pain
I was diagnosed with endometriosis when I had my first laparoscopy at 14. I’m very lucky. I got my period […]
The Obstetrician Who Cried “White Privilege”
In December of 2016, I wrote an essay for Nursing Clio called Nurse-Midwives are With Women, Walking a Middle Path […]
My Story of 20 Weeks
20 weeks. That is the magic number according to the GOP. House Republicans last week passed a bill, which they […]
100,000 Women in Trafalgar Square: Remembering The Forgotten Women’s March of 1979
On January 21 this year, thousands of people rallied in central London in solidarity with the Women’s March on Washington, […]
The Pill Kills: Women’s Health and Feminist Activism
On December 16, 1975, a group of Washington, D.C. area women’s health activists held the first-ever protest at the headquarters […]
A Pot of Herbs, A Plastic Sheet, and Thou: A Historian Goes for a “V-Steam”
The first time I walked into the women’s area of my local Korean spa a few years back, my nose […]
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.
The Slippery Slopes of Burwell vs. Hobby Lobby
by Andrea Milne
Everybody and their sister is blogging about the Burwell vs. Hobby Lobby ruling, so I’ll spare you all the gory details, if for no other reason than to preserve my sanity. Here, in my (admittedly biased) opinion, are the most important things you need to know:
The Boy Who Lived: Stillbirth and Life after Death
Ghostbelly: A Memoir. By Elizabeth Heineman. (New York: The Feminist Press, 2014. 320 pp. $16.95.) How do you grieve for […]
