Health Data Health Policy How To 
Health Populi
MARCH 26, 2025
When his publisher asked him to write a third book on AI in health care still a hot topic in publishing Tom said hed rather turn to a subject long on his mind: the state of health care in America and how to change the conversation on health policy to involve all citizens. appeared first on HealthPopuli.com.
Health Populi
APRIL 6, 2022
He had me at the statement, “I believe health data is medicine.”. Those were the words of Ardy Arianpour, CEO and Co-Founder of Seqster, when sharing with me how his company was founded. In summing up the patient-centered interoperability goal, Ardy summarized: “We’ve created the Mint.com of health data.”
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Health Populi
JUNE 18, 2024
Health care access is a challenge in rural and urban areas, cities and suburbs, and across more demographic groups than you might realize, as we see wait times grow for appointments, primary care shortages, and delays in screening plaguing health systems around the world. ” The post How to Get Better Care to More People?
Health Populi
JANUARY 28, 2020
Most older Americans would share data collected through a wearable tech device with their health care provider, but a minority (35%) would share that information with a health insurance company. One-third of older people wouldn’t share their health data with any third party at all.
Health Populi
OCTOBER 24, 2019
In mode of attendee (and self-confessed collegial-groupie of Dr. Topol’s), I took in his remarks taking notes as fast as I could thanks to Mom teaching me how to type on an IBM Selectric (the significance of which I wrote about here in the Huffington Post ). “The U.S.
Health Populi
APRIL 17, 2023
The bill expands privacy protections for Washington State’s health citizens beyond HIPAA’s provisions. The My Health, My Data Act defines “consumer health data” as “personal information that is linked or reasonably linkable to a consumer and that identifies a consumer’s past, present, or future physical or mental health.”
Health Populi
JUNE 5, 2020
But while the new ONC rules may make it easier for health consumers to access personal health information, the Field of Dreams phenomenon subverts the noble goal: we may “build” a system for people to access health data (like Blue Button), but patients may not “come.” How to deal?
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