Paraquat Gets EPA Thumbs Up: Advocates Get The Agency’s Middle Finger
Paraquat Gets EPA Thumbs Up: Advocates Get The Agency’s Middle Finger
The recent EPA endorsement of paraquat, despite mounting evidence linking it to Parkinson's disease (PD), is a profound betrayal of public trust. This decision, seemingly driven by corporate interests, disregards the health and well-being of communities across the nation, fueling an intensified wave of outrage and disappointment.
The EPA's report, touting the benefits of paraquat for crop production, is a stark slap in the face to those who tirelessly advocate for environmental safety.
Commentary by Larry Gifford
The recent EPA endorsement of paraquat, despite mounting evidence linking it to Parkinson's disease (PD), is a profound betrayal of public trust. This decision, seemingly driven by corporate interests, disregards the health and well-being of communities across the nation, fueling an intensified wave of outrage and disappointment.
The EPA's report, touting the benefits of paraquat for crop production, is a stark slap in the face to those who tirelessly advocate for environmental safety.
The EPA ruling reads, “After a thorough review of the relevant studies, the Agency concluded that the weight of evidence was insufficient to link paraquat exposure from pesticidal use of U.S. registered paraquat products to PD in humans.”
Despite acknowledging the potential link between paraquat and PD, the agency's assertion that benefits outweigh risks feels like a callous dismissal of the suffering and harm inflicted on individuals and families affected by this debilitating disease.
The ruling continues, “Although Parkinson’s Disease (PD) is not an expected result of the pesticidal use of paraquat, a connection has been hypothesized throughout the scientific literature, and so out of an abundance of caution, the Agency conducted a systematic review to assess the relationship between paraquat exposure and PD.”
Well, thank goodness they did a “systematic review” — cue the exaggerated eye-roll. But, unfortunately, the agency must not have read the article which noted exposure to paraquat within 1,600 feet of a home increases risk of developing Parkinson’s disease by 75%, or the University of California, Los Angeles, and the University of Southern California study which found that people exposed to paraquat at a younger age -- in their teen or young adult years -- had an increased Parkinson's risk of 100 to 500 percent, depending on overall exposure. Hmmm… surely The Michael J Fox Foundation included them among the studies and 107,000 signature petition pleading the EPA to ban paraquat.
Golly, I think I know what happened. This is funny. Well, it’s funny, not-funny. Sad, really. Actually a bit embarrassing for the EPA.
The agency didn’t read it.
You read that correctly. They didn’t get around to it. The agency admits it failed to fully consider scientific studies and testimony submitted by the Michael J. Fox Foundation and Earthjustice.
The ruling reads, “First, EPA recognizes that the Michael J. Fox Foundation and Earthjustice submitted letters to EPA on August 4, 2023, along with information that they believe is relevant to EPA’s consideration of paraquat’s health risks. This information consisted of approximately 90 submissions including scientific studies, as well as testimony filed in an ongoing state lawsuit concerning paraquat. While the Agency has started reviewing that material, it was unable to complete that review prior to the issuance of this document.”
The EPA's decision reflects a deeply flawed regulatory process that prioritizes profit over public health. By downplaying the significant risks associated with paraquat exposure, the agency not only undermines its own credibility but also perpetuates a system of injustice that disproportionately impacts vulnerable communities.
More than 10,000,000 pounds of Paraquat is used on U.S. crops each year. Paraquat is the deadliest pesticide used in U.S. agriculture, capable of killing a human with just a sip, as the U.S. Environmental Protection Agency (EPA) warns. For the record, it’s also used in Australia.
Despite the growing body of research linking paraquat to PD, the EPA's insistence on insufficient evidence is a blatant disregard for scientific consensus and the lived experiences of those affected. This dismissal of legitimate concerns only serves to amplify the outrage and disappointment felt by communities who expected better from their government.
In the end, the EPA's approval of paraquat is not just a failure of regulatory oversight but a betrayal of the fundamental duty to protect public health. Until meaningful action is taken to address the risks associated with paraquat exposure, the cycle of outrage and disappointment will persist, leaving communities vulnerable and disillusioned.
Thank you to The Michael J. Fox Foundation for including and representing PD Avengers and other organizations in the Unified Parkinson's Advocacy Council in the EPA filing.
Countries where paraquat is banned or severely restricted
.Austria
Belgium
Belize
Benin
Brazil
Bulgaria
Burkini Faso
Cambodia
Canada
Caribbean
Chad
Chile
China
Columbia
Cote d’Ivoire
Croatia
Cyprus
Czech Republic
Denmark
Dominican Republic
England
Estonia
Finland
France
Gambia
Germany
Greece
Guinea
Guinea-Bissau
Hungary
Iceland
Indonesia
Ireland
Italy
Kuwait
Latvia
Lithuania
Luxembourg
Malaysia
Mali
Malta
Morocco
Mozambique
Netherlands
Niger
Northern Ireland
Norway
Oman
Peru
Philippines
Poland
Portugal
Romania
Saudi Arabia
Scotland
Senegal
Slovakia
Slovenia
South Korea
Spain
Sweden
Switzerland
Taiwan
Togo
Wales
Spark of Change: Igniting Parkinson's Advocacy
Kristi LaMonica PhD seizes advocacy opportunities with U.S. Congresspersons and State lawmakers in New York’s capital city. She is urging support for the National Plan to End Parkinson’s Act and the statewide push for a Parkinson’s registry. Read her first hand account here.
by Kristi LaMonica PhD.
I live about a 20-minute drive north of New York's state capital Troy. This area has become quite the epicenter for Parkinson's advocacy, and I'm fully on board. Last year, Representative Paul Tonko (D-NY), was bipartisan co-sponsor of the National Plan to End Parkinson’s Act. I'm lucky to live right in the district of Representative Tonko. The only downside was that the plan didn't make it to the voting floor in 2022. But hey, the sponsors were true to their word –brought it back in 2023. And once again, Representative Tonko stood strong as a bipartisan co-sponsor.
Following the national plan closely through my PD Avengers connection and the Michael J. Fox Foundation (MJFF), I jumped at advocacy opportunities. My debut was at the end of March when I became part of a small group asked to meet with a staffer from Senator Kirsten Gillibrand's team (D-NY). I was given just three minutes to share my story. The goal was to sway Senator Gillibrand into co-sponsoring the national plan – and she did.
Fast forward a bit, earlier this month, MJFF contacted me again. I was invited to a "Faces of Parkinson’s" roundtable discussion with Senator Tonko and other local advocates. The day kicked off with me on a little parking adventure – street parking can be quite a puzzle. Flustered, I made it to Representative Tonko's office and was relieved to be greeted by familiar faces.
Representative Tonko kicked things off by discussing how support for a National Plan to End Alzheimer’s has done wonders for research and drug pipelines. During this discussion, my dyskinesia acted up and I couldn’t sit still. Honestly, I took it as a good sign. When people with Parkinson’s advocate, we often look too put-together. I believe when we look too good, it works against our cause. It makes it more difficult for people to justify more funding for Parkinson’s. To that point, none of us in the room exactly fit the traditional image of someone with Parkinson's – you know, the stooped, white-haired, elderly man shuffling about.
We covered a lot of ground – from research to medications and nearly everything in between. Talking about the number of diagnoses created the perfect segue into discussing young onset Parkinson’s disease (YOPD), the unique challenges we face and for a request the YOPD community not be forgotten in the National Plan. The struggle to get disability support was brought up, and the research gap concerning women and hormones got its moment in the spotlight. I made sure to let Representative Tonko know that data from the PD Avengers and Fox Insight Experiences of Women with PD survey is open access via Fox Den. For researchers, it's like a treasure trove of preliminary data for grants. Overall, our meeting was a success. We didn't have to convince Representative Tonko to stand with us, but we did manage to introduce him to some new aspects.
Yesterday, another email from MJFF landed in my inbox. I'm in for a meeting with Senator Chuck Schumer's staffers (D-NY) on September 5th. It syncs perfectly with my teaching schedule, so of course, I'm saying yes!
In addition to advocating for the National Plan, I was invited to speak at a press event at the state capital to support a state registry for people with Parkinson’s. I was not feeling my best that day. I was off. And I wasn’t on by the time I had to leave. It was the first time I had to ask my husband to drive me anywhere. On the way to the event, I ditched my prepared speech and just spoke from the heart about the challenges Parkinson’s gave me that day. The bill unanimously passed the state senate but unfortunately the New York State Assembly did not take up the bill.
I implore each of you to reach out to state lawmakers in support of state registries across the country for Parkinson’s disease.
EDITOR’S NOTES: There is not a national registry for Parkinson’s in the United States. But there is a plan afoot. The goal is for each state to establish its own registry and feed the data into the Center for Disease Control's National Neuro-logical Conditions Surveillance System, which tracks the incidence and prevalence of many neurologic disorders, including Parkinson's.
If you would like to learn more about state government relations and how you can be involved in advancing work toward a cure for Parkinson’s, please register for the second annual State of the States webinar: 50 States, 50 Legislatures, and Thousands of Pieces of Legislation. Join the Michael J. Fox Foundation Policy Team on Wednesday, August 30 for a discussion on legislative wins, losses, and lessons learned along the way in state legislatures across the U.S. You can register for the webinar here.
Kristi LaMonica’s Advocacy Journey: Insights for All
We can learn valuable lessons from Kristi LaMonica's adventures in advocacy.
Local Impact Matters: Living near Troy, New York's capital, taught Kristi the power of local advocacy. Change begins at home and radiates outward, creating tangible impact.
Resilience Brings Results: Despite delays, the National Plan to End Parkinson's Act's reintroduction in 2023 reflects the strength of persistence in advocacy.
Brevity Packs Punch: In her first speech to Senator Gillibrand's staffer, Kristi learned the might of concise, heartfelt messages to spur action.
Authenticity Over Perfection: Participating in a "Faces of Parkinson’s" discussion highlighted authenticity's power. Openness, not challenges, strengthens advocacy.
Inclusion is Vital: Advocating for the entire Parkinson's community, especially young onset patients, ensures equitable attention and boosts advocacy.
Stories Leave Impact: Sharing personal experiences, from accessing disability support to women's research gaps, enriches advocacy conversations.
Diverse Strategies Succeed: Engaging with officials in various contexts underscores the versatility of advocacy approaches.
Seize Opportunities: Amid personal challenges, speaking for a state registry showcased authenticity's resonance.
Collaboration Amplifies: Working with PD Avengers and Michael J. Fox Foundation emphasizes collective advocacy strength.
Incremental Steps Matter: State senate bill success proves small actions accumulate to significant change.
As Kristi LaMonica PhD. readies for Senator Schumer's staff discussion, her journey underscores every voice's importance and the impact of any contribution, no matter its size. Authenticity, seizing moments, and collaboration fuel her impactful advocacy.
Suggested Reading: Big wins and Next Steps in State Advocacy
PD Avengers Assemble - July 2022
Updates on Paraquat Lawsuits, PMD Alliance’s “All In” Conference, the inaugural Improv for Parkinson’s Summit, Every Victory Counts guide now available in Canada thanks to a collaboration between Davis Phinney Foundation and Parkinson’s Canada and more.
PD Avengers, if you missed July’s PD Avengers ASSEMBLE meeting, here’s the video.