A new law quietly passed last December contains a waiver of informed consent that eliminates the requirement of pharmaceutical companies to let you know if a medication or vaccine given to you or your child is experimental.
Wow. One last Christmas surprise from President Obama.
This is according to Section 3024, “Informed Consent Waiver for Clinical Investigations” of H.R. 32, the “21st Century Cures Act.” Here’s the wording of the text:
Clinical testing of investigational medical devices and drugs no longer requires the informed consent of the subjects if the testing poses no more than minimal risk to the subjects and includes safeguards.
“Clinical testing” is not clearly defined. Furthermore, who the heck gets to decide what “minimal risk” is? The pharmaceutical companies? The FDA? Medical professionals? How incredibly patronizing.
I don’t know about you, but before taking medication or allowing my children to, I want to know all of the details. What are the risks? What are the potential side effects? What is the worst thing that could happen if we don’t take it?
I want to be fully informed and make my own decision, and anything less than that is a type of condescension that makes my blood boil. My children and I are not Big Pharma’s lab rats.
I hadn’t heard a thing about this until my friend Melissa from Truthstream Media send me the horrifying video below and I knew that I had to let you folks know right away. Sign up here to stay up to date with the latest news and information that relates to your freedom and well-being.
This video is a must-watch and explains it in far more detail.
Daisy is a coffee-swigging, gun-toting, homeschooling blogger who writes about current events, preparedness, frugality, and the pursuit of liberty on her websites, The Organic Prepper and DaisyLuther.com She is the author of 4 books and the co-founder of Preppers University, where she teaches intensive preparedness courses in a live online classroom setting. You can follow her on Facebook, Pinterest, and Twitter.