Summary:
In her memoir Ask Me
About My Uterus, science writer Abby Norman tells two intertwined stories:
one about her fraught relationship with her own chronically ill body, and another
about the fraught relationship between women and medicine. Norman is a
sophomore at her dream college when a sudden, unrelenting abdominal pain sends
her to the emergency room—and into a revolving door of medical appointments for
years to come. Thus begins her diagnostic odyssey, protracted by an infuriating
obstacle: not only must she endure excruciating pain, she must convince doctors
that it’s real.
Norman is eventually diagnosed with endometriosis but has
several frustrating clinical encounters along the way. Her symptoms are
repeatedly minimized or disbelieved by doctors of various identities and
specialties. One actually says the words that have long been inferred to Norman
and so many women before her: “This is all in your head.” Finally receiving an
accurate diagnosis provides some measure of clarity about Norman’s pain but
little in the way of relief. She learns firsthand that medical knowledge about
endometriosis is desperately lacking—a troubling realization given its prevalence.
A commonly cited statistic suggests one in ten women have endometriosis but, as
Norman notes, most studies have excluded marginalized communities, so the
incidence is likely higher. Norman ultimately becomes an expert on the
condition, setting her on a path to advocate for herself and others with
endometriosis—and to write about it.
The memoir is organized chronologically, beginning with the
onset of Norman’s symptoms about seven years prior to the book’s publication, with
occasional flashbacks that draw connections between her current crisis and her
difficult childhood. She opens several chapters with descriptions of famous
case studies and experiments, situating her own experience within a long and
disturbing lineage of women dismissed, misdiagnosed, and mistreated by medical
professionals.
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