Supplements have long been the objects of attack by Big Pharma, as most of them are natural and cannot be patented, threatening the huge profits made from much more toxic pharmaceutical products. The medical industry has long desired to bring supplements under government control, so they could either ban them outright or further refine them into patent-able products from which they could then profit from. But with strong consumer action preventing legal action (so far) to ban supplements or regulate them, it would appear the medical system is now taking matters into their own hands and banning them outright. The Children’s Hospital of Philadelphia became the first hospital in the country to ban supplements from being dispensed to patients. So patients at this hospital will no longer have access to such supplements as probiotics, vitamins, minerals, digestive enzymes, herbs, etc.
In new trade talks between the US and the European Union, we need to make sure “harmonization” doesn't make our supplement laws like theirs. Last March, the Obama Administration announced its intention to enter into Transatlantic Trade and Investment Partnership (TTIP) negotiations with the European Union (EU) to increase trade and investment between the two regions. According to the White House fact sheet, the goal of the negotiations is to boost economic growth in the US and EU, and increase jobs supported by transatlantic trade and investment. One of their stated aims is to reduce costly “behind the border” non-tariff barriers that impede the flow of goods, including agricultural goods. What we do not want to see a threat develop to our access to a wide range of higher-dose supplements or to legitimate health claims on products. With increasing harmonization of laws worldwide, it is important for us to fight back against inappropriate regulation of natural products among our trading partners. Inevitably, our regulatory agencies will come under pressure to conform, when trading partners adopt more restrictive policies.
Just as Congress is preparing to recess until the second week in September, Sen. Dick Durbin (D-IL) reintroduced legislation that would deal a deadly blow to nutritional supplements. This bill is a naked new FDA power grab—an attempt to move us one step closer to a full FDA pre-approval system for supplements. That, of course, would just make supplements insanely expensive, like drugs—if you could get them at all.
Ubiquinol, the reduced form of CoQ10, effectively rescues cells from the damage caused by a statin drug thereby protecting muscle cells from myopathies. Patients with statin-associated myopathy who took CoQ10 experienced significantly less pain, decreased muscle weakness and cramps, and less fatigue. Ubiquinol is not only important for those taking statins, it’s also been found to lower the risk of a variety of chronic diseases and has anti-aging properties.
Cardiovascular disease is the #1 cause of death within industrialized societies. A recent study published in the International Journal Cardiology indicates that aged garlic extract, in combination with vitamin B12, folic acid, vitamin B6 and arginine, is capable of favorably altering the ratio of brown to white adipose (fat) tissue surrounding the heart muscle, reducing homocysteine (a blood vessel damaging amino acid) and slowing the progression of coronary artery calcification in human subjects.
Make no mistake, there is a well orchestrated campaign underway to take away your rights and access to vitamins and supplements. Illinois Senator Durbin is planning to reintroduce his supplement bill, the Dietary Supplement Labeling Act (S 1310), which would grant more power to the FDA to regulate dietary supplements like they were drugs.
Dr. Paul A. Offit, chief of the infectious diseases division of the Children’s Hospital of Philadelphia, thinks vitamins should be treated as drugs, stating that people receive enough nutrients through their regular diet and do not need supplements. He ignores data that conflicts with his agenda and only cites studies that suggest negative effects of supplementation and excludes important evidence to the contrary. This approach could very well be due to the fact that he will soon be publishing a book bashing alternative medicine.
A new NIH study proclaiming that Ginkgo biloba causes cancer is so absurd you must wonder if they produced it with a straight face. More important, though, is why—and the reason is truly frightening. It’s part of a system determined to steal all natural health methods and hand them to Big Pharma & Big Medicine for profits.
Senator Orrin Hatch (R-UT) and three of his colleagues have introduced S 1031, a bill that would allow Health Savings Account (HSA) funds to go toward dietary supplements without having to get a doctor’s prescription; the same would apply to Health Flexible Spending Accounts (FSAs). The legislation, called the Family and Retirement Health Investment Act of 2013, does this by expanding the term “medical care” to include dietary supplements, and it would allow spending up to $1,000 each year. A companion bill, HR 2194, was introduced in the House by Rep. Erick Paulsen (R-MN).
Alzheimer’s disease is currently at epidemic proportions. It’s becoming increasingly clear that what you eat, or don’t eat, can influence your risk as well as the rate at which the disease progresses. B group vitamins, in particular, especially folic acid and vitamins B6 and B12, are again making headlines for their powerful role in preventing Alzheimer’s disease. B vitamins may reduce brain shrinkage by up to 90 percent!