A Rare Disease True Crime Story
Sometimes truth is stranger than fiction, and rare disease is a mystery for most people, including those who have it. At a mystery writers conference I attended in Boston, one of the presenters was a Medical Examiner, who served as the consultant for the TV show, Crossing Jordan. She shared her unusual cases with the audience, who were looking for realism and inspiration for their writing.
My ears perked up as she spoke about a terrible story that occurred in 1989 when a woman named Patricia Stallings brought her baby into the ER after the child was vomiting and having difficulty breathing. As the doctors examined the baby, they found high levels of ethylene glycol in the child’s blood, which they suspected was due to antifreeze poisoning. As a result, they removed the child from the mother’s care. Four days after the mother visited her child in foster care, the child became very ill again, and the mother was arrested. The child died shortly after, and the mother was convicted for her son’s murder.
While serving a life sentence in prison, she gave birth to another child. The child was placed in foster care, but soon the second child also started having symptoms. The medical examiner was called in to study the baby’s bottle, to find proof it had been tampered with poison. After further analysis of the blood with a biochemistry professor, the examiner realized what was misidentified as ethylene glycol was actually propionic acid. The medical examiner remembered a lecture she had in medical school about a genetic disease that caused the body to produce propionic acid, and, after consultation with specialists, the baby was diagnosed with methylmalonic acidemia (MMA).
The mother served two years in prison before being released in 1991, following proof that the lab testing of the blood samples of the first child had mistakenly identified propionic acid as ethylene glycol, and that he had MMA.
This story is a cautionary reminder of the many kinds of challenges that people living with rare diseases have faced. Fortunately, with prenatal screening tests available in most states, rare diseases, such as methylmalonic acidemia (MMA) and propionic acidemia (PA), are being diagnosed sooner. With better diagnostics and research into these diseases, we can only hope that, in the future, stories like the one of Patricia Stallings will serve as historical or fictional inspiration.
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Nina Wachsman
Nina is the co-founder and president of Know Rare
Nina’s experience goes across therapeutic categories from rare disease like pulmonary arterial hypertension (PAH), autoimmune disease and cancer, and her expertise ranges from market research and strategy to patient and digital marketing.
Additionally, she has been a founder and angel investor of a biotech start-up, helped brand an oncology patient organization, Aim at Melanoma, and worked on patient education for Genentech’s leading HER2 therapy, Herceptin.
Nina is also a mother, grandmother, artist, and author of The Gallery of Beauties, a novel set in the Venice in the early 17th century.