3 Privacy Concerns Patients May Not Know About
ST. PAUL, Minn.—Citizens’ Council for Health Freedom (CCHF) is alerting Americans to three privacy issues they may not know anything about. Groundbreaking New Book on the Dangers of Electronic Health Records (EHRs)
ST. PAUL, Minn.—If you’ve ever been in the doctor’s office and the clinician isn’t looking you in the eye—but at a computer screen instead—you know how electronic health records (EHRs) have impacted the medical industry. But this lack of patient-doctor interaction due to EHRs is just the tip of the iceberg.
CMS Plan for ‘Direct Primary Contractors’ Will Confuse Public / Compromise DPC Clinics
ST. PAUL, Minn.—Patient privacy advocate Citizens’ Council for Health Freedom (CCHF) has spoken out about the Centers for Medicare & Medicaid Services’ (CMS) potential plan to wrap direct primary care contracting (DPC) clinics back into the government. Renaming ‘Meaningful Use’ Won’t Free Doctors or Protect Patient Privacy
ST. PAUL, Minn.—The Center for Medicare & Medicaid Services (CMS) is renaming the “Meaningful Use” program. The newly named “Promoting Interoperability” program will include revamped programs toaddress electronic health records (EHRs) interoperability, physician reporting requirements and hospital price transparency.
What’s the Problem with EHRs? 347,000 Data Breaches Since 2009
ST. PAUL, Minn.—The implementation of theHealth Information Technology for Economic and Clinical Health Act in 2009 was a blow for health freedom. HITECH, embedded within the Recovery Act, provided at least $27 billion to establish a National Health Information Network for data sharing without patient consent. HITECH requires doctors and hospitals to use government-certified electronic health records (EHRs) or face financial penalties. Minnesota Legislators Voting on Crucial Patient Privacy and Consent Bill Thursday
ST. PAUL, Minn.—Citizens’ Council for Health Freedom (CCHF) is alerting Minnesota residents about a crucial legislative vote Thursday that will impact medical privacy and patient consent rights. Revised Common Rule Strips Parents of Consent Rights Re: Baby DNA Used for Research
ST. PAUL, Minn.—As things stand, in just over two months parents will lose their consent rights for the use of their newborn baby’s DNA for federally funded research, once the revised Common Rule goes into effect on July 19, 2018.
CCHF Connects with Lawmakers on Patient Privacy, Opioid Crisis
ST. PAUL, Minn.—Citizens’ Council for Health Freedom (CCHF) is reaching out to lawmakers regarding two matters in the ongoing “opioid crisis.”
First, CCHF sent a letter to leaders of the House Energy and Commerce Committee, urging them to keep private the medical records of those undergoing substance abuse treatment.
New Parent Lawsuit Exposes Stolen ‘Baby DNA,’ Says Citizens’ Council for Health Freedom
ST. PAUL, Minn.—Citizens’ Council for Health Freedom (CCHF) is applauding a new lawsuit where a group of parents are suing the state of Michigan for “stolen blood” because the Michigan BioTrust for Health stores Baby DNA for research—without parental consent. World Aghast at Facebook Data Scandal, But HIPAA Shares Private Patient Data Every Day
ST. PAUL, Minn.—Headlines exploded when it was discovered that Facebook may have had a role in allowing a UK-based political data firm that worked for Donald Trump’s presidential campaign to improperly access data on 87 million people, CNN, among others, reported. Less than a month later, CNBC reported Facebook had a plan to match Facebook user data with patient data, which was put on hold after the previous leak was discovered. Follow Us on Social MediaFollow Us
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Health Privacy Alert!
HIPAA DOES NOT PROTECT PRIVACY... AND YOU ARE By federal law, you are not required to sign the clinic or hospital HIPAA "Privacy" form (or the Acknowledgement of the Notice of Privacy Practices embedded in consent forms)...even if the clinic tries to insist that you must.
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