Updated Oct 24, 2026
/Jeff Garlin reveals suicide plan during 'The Goldbergs' exit/Vistra Shares Rise on $4.2 Billion Nuclear Loan Commitment/Andrew Luster, Max Factor heir and serial rapist, released from prison/Family recounts naming inherited disease that altered household dynamics/Dana Senaha shares family experience with new pancreatic cancer drug/Pathos raises $237 million in Series E led by Bristol Myers Squibb/Jeff Garlin reveals suicide plan during 'The Goldbergs' exit/Vistra Shares Rise on $4.2 Billion Nuclear Loan Commitment/Andrew Luster, Max Factor heir and serial rapist, released from prison/Family recounts naming inherited disease that altered household dynamics/Dana Senaha shares family experience with new pancreatic cancer drug/Pathos raises $237 million in Series E led by Bristol Myers Squibb

Family recounts naming inherited disease that altered household dynamics

A personal account details how a family's unnamed inherited condition, referred to only as "it," was finally identified, changing their understanding of the illness. The narrative describes the symptoms experienced by the author's mother, including hand tremors and word loss, as well as periods of unreachability. The condition had a history in the family, with the author's grandmother dying at age 29 of what the family believed was a similar ailment. The author's mother showed symptoms before the author was old enough to ask questions, while the author's older sister received a diagnosis at age 26. In the household, the disease was characterized by a pronoun rather than a medical term, used in phrases like "it got worse over the winter" or "we don't know much about it." The story highlights the shift from vague descriptions to a specific name for the condition.

By Hannah Voss2 min read
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A personal account details how a family's unnamed inherited condition, referred to only as "it," was finally identified, changing their understanding of the illness. The narrative describes the symptoms experienced by the author's mother, including hand tremors and word loss, as well as periods of unreachability. The condition had a history in the family, with the author's grandmother dying at age 29 of what the family believed was a similar ailment. The author's mother showed symptoms before the author was old enough to ask questions, while the author's older sister received a diagnosis at age 26. In the household, the disease was characterized by a pronoun rather than a medical term, used in phrases like "it got worse over the winter" or "we don't know much about it." The story highlights the shift from vague descriptions to a specific name for the condition.