President-elect Trump wants measurable impacts toward ending chronic disease within two years. Mr. Kennedy emphatically replied, "Mr. President, I will do that."
Everyone is arriving on the scene with suggestions on how he should make America healthy. The media focus on the dangers of processed foods, but are dead silent on the fact that Congress should repeal the extraordinary protections available for vaccine manufacturers under the National Childhood Vaccine Injury Act of 1986, and the PREP Act.
Here is what I see as the main hindrances to our achieving optimal national health by 2027.
Vaccines
Vaccines are obviously the primary cause of the childhood chronic disease epidemic. Four years ago, attorney Greg Glaser and I filed a petition in federal court to bring to the President's attention the fact that a control group study and a pause on vaccine mandates is imperative or our national security would be in peril.
Food Ingredients
Pharma controls much of the FDA-approved vitamin ingredient, preservative, coloring, and additive market. Promoting healthier choices by banning harmful ingredients is difficult since big pharma is implicated.
Growth hormones for cattle and sheep
Since the 1950s, the FDA approved steroid hormone drugs such as natural estrogen, progesterone, testosterone, and their synthetic versions. It is impossible for me to believe these alterations don't negatively impact our health.
Bovine Growth Hormones
Bovine somatotropin (bST) is an FDA approved drug to increase milk production in dairy cows. The FDA determined that milk and meat from these cows is safe for humans to eat.
Food Irradiation
Unbelievably, FDA approved gamma rays emitted from radioactive forms of the element cobalt (Cobalt 60 is a byproduct of a nuclear reactor) or of the element cesium (Cesium 137 produced by nuclear fission in nuclear reactors), X-rays produced by reflecting a high-energy stream into food, or a high-energy electron beam propelled from an accelerator into foods including: beef and pork, crustaceans, fresh fruits and vegetables, lettuce and spinach, poultry, seeds for sprouting, shell eggs, shellfish, spices and seasonings.
Pasteurization
Ultra-high temperature processing (UHT) is an FDA-approved food processing technology that sterilizes liquid food by heating it above 284 °F.
Pascalization
HPP is a non-thermal food preservation technique using intense pressure for a certain time to preserve juice for up to 60 days. Commercial cold-pressed juices are not raw, but the public believes that this juice is made through a pressing method. It is not.
Pesticides
The EPA and the FDA share responsibility for the oversight of pesticide chemical residues in food. The EPA also establishes tolerances, and the FDA enforces them.
GMOs
GMO is the common term that describes foods that have been created by genetic engineering. The list of GMO crops is extensive.
Lobbying
Interest groups spent a record $4.2 billion lobbying federal lawmakers in 2023, led by the pharmaceutical and health products industries. OpenSecrets estimates health companies spent over $739 million for the year.
DSHEA
Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), the FTC and the FDA share jurisdiction over the marketing of herbs and dietary supplements. They took away the ability of dietary and herbal supplement manufacturers to convey truthful information that their products can treat, cure, or prevent any disease. What is permitted is 'window dressing' that only describes how a nutrient or dietary ingredient affects the normal structure or function of the human body.
What must be done?
An outright prohibition on the standard unhealthy lifestyle is out of the question. Radical changes could wipe out entire industries. Action must not only be precise, but must remain cognizant that a half of a century of bad choices cannot be easily erased in two years.
Although well intended (I hope) most of the standard suggestions will have a negligible impact at best if these lesser-known culprits are ignored. Rather than initiate a congressional investigation on the harms of breakfast cereals, I hope these issues are thoroughly examined.
Great points! On the vaccine front, here are some policy changes that would not require action by Congress
• TRUTH. End the public health information war by replacing censorship, propaganda, and secrecy with transparency and truth.
o End censorship.
o Make federal public health data and analysis public, without years of FOIA litigation. Require pharma companies (rather than tax-payers) to bear the cost of preparing licensing documents for immediate publication after a license is granted.
o Stop funding propaganda. End the flow of HHS grants (millions and millions of $$!) awarded for efforts to manipulate public behavior, especially with regard to vaccines.
o Bring truth to government pronouncements regarding public health. Remove the false information currently plaguing the websites of public health agencies, and replace it with truth. Enforce the Information Quality Act.
• ACCOUNTABILITY AND COUNTERMEASURES.
o End/limit liability shields for manufacturers of “countermeasures” by terminating all current PREP Act declarations.
o Terminate all Emergency Use Authorizations.
o Enforce existing laws regarding manufacturing, purity, labeling, and fraud; refer criminal wrongdoing to DOJ.
o Make CICP functional.
Revise regulations to ensure transparency and due process.
Revise regulations to extend the filing deadline.
Promulgate an injury table for C19 shots.
Fully staff program, and seek sufficient funding from Congress.
• SCIENCE. Do not allow any clinical trial to support authorization or licensure unless it has the following features:
o The entity/individuals conducting the trial have no financial interest in the product;
o The trial is randomized, double-blinded, and uses a true placebo control;
o The trial remains blinded for a period of time sufficient to meaningfully assess both efficacy and safety;
o The trial is powered by enough participants to meaningfully assess both safety and efficacy;
o The trial is reviewed and assessed in a written report by a panel of experts with no financial or other interest in the product or in the product’s manufacturer;
o All data from the trial (minus identifying personal information) are made immediately available to the public for independent analysis, along with the names of all entities and individuals who conducted or reviewed the trial and their written reports.
Damage done from the jabs. Apparently 200 million sheep took it! Can’t reverse the damage. I know people who were paralyzed, have cancer, stroked out, auto immune diseases, etc all from the convid jab. These can’t be reversed! Their lives are forever ruined. They would have made America healthier by not poisoning them!