Monthly Archives: May 2017

Podcast: You Make Me Sick! Nature-rich lives and the future of environmentalism

For this month’s episode of You Make Me Sick, we broke from our usual discussion of things that might harm your health to talk about an exposure that might help your health. Specifically we talked with journalist and advocate Richard Louv about the ways in which exposure to green spaces can affect your health. Mr. Louv, author of Last Child in the Woods and The Nature Principle and founder of the non-profit Children and Nature Network, sat down with us to discuss the need to design nature rich lives and the future of environmentalism.

Want more? Subscribe to us on iTunes or Google Play, or check out our SoundCloud to listen via desktop! [Image credit Francisco Anzola]

Posted in Health science / Tagged | Comments are closed

Toxic secrets in our food? EDF joins in lawsuit aimed at protecting food safety

Today, Environmental Defense Fund joined other groups in challenging a Food and Drug Administration (FDA) rule that allows chemical and food manufacturers to decide for themselves – in secret – what chemicals and food additives can be added to foods. The practice puts our health at risk and does not fulfill Congress’ requirement that FDA determine that chemical additives are safe before they can be used in food.

Americans would be shocked to learn that food companies routinely add novel chemicals to our food without first getting FDA approval. In doing so, the companies are exploiting a loophole exempting ingredients “Generally Recognized as Safe” (GRAS) from formal FDA review and approval.

Originally intended for ingredients like vinegar and olive oil, industry now abuses the GRAS loophole by bypassing FDA review and making safety determinations in secret. The alarming result: even FDA does not know what is in our food. In fact, FDA has no way to know what chemicals are actually being used in which food or in what quantities—even in baby food.

Last year, the FDA issued a final rule formalizing this outrageous practice. We described this decision as a lost opportunity for safer food additives when the decision was made. Today, EDF and our colleagues at the Center for Food Safety (CFS), Breast Cancer Prevention Partners, Center for Science in the Public Interest, and Environmental Working Group, represented by CFS and the environmental law firm Earthjustice, joined in filing suit against the FDA for unconstitutionally and illegally delegating that authority to self-interested food and chemical manufacturers.

It is disappointing that the groups were forced to take legal action. In addition to being a bad policy that doesn’t comply with law, or protect public health, the FDA is oddly out of touch with public sentiment. Just last week an industry funded survey showed overwhelming consumer concern about chemicals in food, including cancer causing chemicals, while showing diminished confidence in the food supply. This continues a trend that has been building for years. Food companies would be wise to take notice: adding secret chemicals without FDA scientific review to our food is no way to improve confidence in their products.

But with thousands of secret chemicals in our food, we can’t wait for industry or FDA to wise up. Today’s lawsuit seeks to force FDA to do what should be common sense—determine that food additives are safe before they can be added to our food.

Posted in FDA, Food, General interest / Tagged , | Comments are closed

Red tape and over-reach: That is the Regulatory Accountability Act, in a word – and a graphic

Richard Denison, Ph.D., is a Lead Senior Scientist.

I blogged last week about the new-but-not-improved Senate Regulatory Accountability Act (RAA), focusing on how it would reinstate some of the worst flaws of the old Toxic Substances Control Act (TSCA) that were fixed in the bipartisan TSCA reform legislation, the Lautenberg Act, signed into law last June.

Here are a few additional things to note.  This bill is scheduled to be marked up next Wednesday in the Senate Homeland Security and Governmental Affairs Committee (HSGAC).

I noted in my last post that RAA is sweeping in scope, and would affect dozens of federal laws and protections in one fell swoop.  My colleague Martha Roberts has just put up a blog post that illustrates this incredibly broad reach by providing a few tangible examples of protections that would be at risk if RAA were to be enacted.

And talk about red tape:  I’m including below her updated graphic depicting the vast bureaucracy RAA would create that all federal agencies would be forced to navigate (click on the thumbnail to enlarge it).

Posted in Health policy, Regulation, TSCA reform / Tagged , | Comments are closed

Toxic Exposures: 10 Americans expose the toxic chemicals in our environment

Every day we are exposed to potentially hazardous chemicals we can’t see —chemicals used in everything from the clothes we wear to the lotions we use and even the couch we sit on. Synthetic chemicals are used to make 96% of products in the United States. Yet scientific research continues to link chemicals in common use to health effects like cancer, infertility, and asthma.

EDF selected 10 individuals across the country to wear a novel wristband technology designed to detect chemicals in their environment for one week – including Gordon, Karen, and Averi.

 

Gordon is a lieutenant for the Memphis Fire Department. Gordon’s wristband detected 16 chemicals, including gamma-chlordane, a pesticide that has been banned in the U.S. since the 1980s, and 3,4-dichlorophenyl isocyanate, a “chemical intermediate,” which is reportedly used exclusively for chemical manufacturing processes. While there were no fires to fight the week he wore the wristband, Gordon wondered if he came into contact with these chemicals from a site visit to a location that formerly housed chemical stockpiles, his local auto repair shop, the nearby highway – or even his fire suit.

Read More »

Posted in Emerging testing methods, Environment / Tagged | Comments are closed

Our health protections at risk: TSCA reform undone by “regulatory reform”?

Lindsay McCormick is a Project Manager. Richard Denison, Ph.D., is a Lead Senior Scientist.

On February 24th, President Trump signed Executive Order 13777, calling on all government agencies to recommend regulations for “potential repeal, replacement, or modification.” As of this writing, EPA has received 46,050 comments on its regulatory reform process. Interestingly, the overwhelming majority of these comments come from individuals across the country voicing their support for strengthening EPA’s regulatory protections, demonstrating that Americans stand strong in their opposition to regulatory roadblocks and rollbacks.

In compliance with this executive order, EPA held a stakeholder meeting last week to identify “regulatory reform” opportunities under the Toxic Substances Control Act (TSCA).

The irony – and absurdity – of this process is that not even a year ago, Congress passed, with overwhelming bipartisan support, sweeping reforms to TSCA, finally providing EPA with new tools and authority to review and manage chemicals more effectively. The need for a credible regulatory agency—one able to make timely, independent, science-based decisions about chemical safety—was seen by all parties as essential to increase public confidence in the safety of chemicals. Under-regulation, not over-regulation, has been the clear problem in this arena for decades.  Read More »

Posted in Industry influence, Nanotechnology, Regulation, TSCA reform / Tagged , , | Comments are closed

New but not improved: The new Regulatory Accountability Act would severely threaten TSCA implementation and many other vital health protections

Richard Denison, Ph.D., is a Lead Senior Scientist.

Last week, as anticipated, Senator Rob Portman introduced his updated Regulatory Accountability Act (RAA).  Sens. Hatch, Heitcamp and Manchin cosponsored the bill.

While it’s new, it can’t be said it’s improved.  Some problems raised with Sen. Portman’s earlier version of the bill were addressed but many were not and quite a few new very problematic provisions were added.

In March, I blogged about the irony that RAA would reinstate a number of requirements that Congress just last June removed from the old Toxic Substances Control Act (TSCA) through the Lautenberg Act amendments that were enacted with overwhelming bipartisan support.  Unfortunately, many of those problems remain with Sen. Portman’s new version of RAA.  And, those flawed requirements would be imposed across the entire federal government, effectively rewriting dozens of federal statutes simultaneously.

I have updated my earlier analysis of RAA vs. the new TSCA to reflect the new version of RAA.   Read More »

Posted in Health policy, Regulation, TSCA reform / Tagged , | Comments are closed