Citizens’ Council for Health Freedom Says Americans’ Private Health Data is Already at Risk and Forced Interoperability Will Make Gaining Access Even Easier
ST. PAUL, Minn.—One lawmaker is pushing for a bill that will require all Electronic Health Records (EHRs) in the country to work together and be able to communicate from system to system.
The Minnesota House of Representatives Civil Law and Data Practices Committee, held an informational hearing to learn more about protecting patients’ health information in the state.
The morning’s presentation, titled “Protecting Medical Privacy in Minnesota,” included testimony by CCHF on protecting patients’ rights and data and the threats to Minnesota’s current privacy protections as a result of efforts to repeal the state’s privacy law by requiring the state to conform to HIPAA.
Citizens’ Council for Health Freedom Releases New Report on Newborn Data Collection; Says Birth Certificates and Newborn DNA Storage Pose Double Threat
ST. PAUL, Minn.—There’s something expectant parents should know about the private, sensitive information being shared at the hospital at the time of their baby’s birth.
I hereby petition the Minnesota Legislature and Governor Dayton to give me and my doctor a choice to protect privacy and autonomy by REPEALING the Minnesota EHR Mandate Law.
ST. PAUL, Minn.—The birth of a baby is a joyous time, filled with activity, questions from new parents and lots of information sharing—especially at the hospital.
But during that somewhat stressful time, precious private information about these new little lives will be shared with countless others, through a seemingly harmless document—the birth certificate.
Citizens’ Council for Health Freedom (CCHF, www.cchfreedom.org), a Minnesota-based national organization dedicated to preserving patient-centered health care and protecting patient and privacy rights, recently released a new report, called “Not Just a Birth Certificate: How states use birth certificates to collect data, conduct research and warehouse electronic health information.”
The President wants your genetic code. Mr. Obama has announced a new “Precision Medicine Initiative” (PMI) that includes databasing medical records, genetic blueprints and lifestyles of a million or more Americans. Here are seven disturbing aspects of his initiative:
Patient Advocate Says New Mandate Will Harm Doctor-Patient Relationships; Survey Demonstrates Concern
ST. PAUL, Minn.—When Minnesota rang in the new year, the state also ushered in a new mandate requiring all health providers to utilize an Electronic Health Record (EHR) system that will share their patients’ private data with other entities and greatly impact the doctor-patient relationship.
ST. PAUL, Minn.—This past year was perhaps one of the most crucial in history regarding patient rights and privacy, as important issues such as government health care, the storage of and research on baby DNA and federal biosurveillance plans all made headlines.
Monday, CCH Freedom released our first publication of stories on “The HIPAA Privacy Deception.” In short, there’s no privacy. HIPAA is not what people think it is. The 12 stories came from people who legally refused to sign the so-called “HIPAA privacy form” at their clinic or hospital.