After a string of successes in 2023, The Michael J. Fox Foundation’s (MJFF) Public Policy team approached this year’s state legislative sessions with two goals: To build on wins to date and to introduce new ways for lawmakers to support the Parkinson’s community in their states. 

This year, we saw an expansion in state Parkinson’s registries, improved insurance coverage for biomarker testing, new genetic testing protections, increased environmental advocacy and more.  

With most legislative sessions now closed, join us in celebrating our wins and laying the groundwork for continued advocacy in 2025. Don’t forget to sign up to get opportunities to advocate in your home state! 

Creating Parkinson's Research Registries

Statewide population-based registries are rich data sources that can fuel research and help researchers, clinicians and policymakers better understand Parkinson's and how to treat it by: 

• Identifying high-risk groups and supporting patient contact studies. 

• Determining accurate incidence and prevalence rates by state.  

• Studying patterns of the disease over time.  

• Improving understanding of links between Parkinson’s and risk factors such as pesticide exposure and military service.  

In 2022, when MJFF began lobbying state lawmakers and rallying local advocates in earnest, just four states had Parkinson’s disease registries. Today, that number is up to 14, with Connecticut, Massachusetts and New York passing legislation this year! 

Increasing Access to Biomarker Testing  

Analysis of tissue, blood and other substances, known as biomarker testing, can provide patients with critical information about their health. While most applications of biomarker testing are in oncology or autoimmune diseases, there is research underway to benefit people living with Parkinson’s and other neurological diseases.  

We urge states to require health plans, including Medicaid, to expand access to this important health care tool by covering the cost of biomarker testing for all conditions, including Parkinson’s. This year, Colorado, Connecticut, Florida, Indiana and Iowa passed legislation to do so, bringing the total number of states ensuring access to biomarker testing to 19.

Expanding Genetic Testing Protections

Federal law prohibits health insurers from using information from genetic testing — like the presence of a gene mutation linked to a neurological disorder — to deny coverage or engage in price discrimination. However, these federal protections do not extend to life insurance, long-term care insurance and disability insurance coverage. The good news: Local lawmakers can fill this gap for their constituents by passing state legislation.  

Louisiana did just that, enacting a law that prohibits insurers from increasing premiums or denying, canceling, limiting or refusing to renew coverage based on genetic testing results. In addition, Nebraska passed the Genetic Information Privacy Act which prohibits direct-to-consumer testing companies from disclosing genetic test results to insurers and employers without consent. 

New This Year: Advocating for Environmental Policy Change

For more than a decade, MJFF has joined advocates and partner organizations across the country to call for the ban of harmful chemicals, including trichloroethylene and paraquat, which may increase Parkinson’s risk by up to 500 percent.

For the first time in 2024, MJFF took our environmental advocacy to the state level by joining forces with the Center for Biological Diversity, Farmworker Justice and the Environmental Working Group to advocate for a California bill that would make the state the first in the U.S. to ban paraquat. 

The final legislation was amended to instead require the California Department of Pesticide Regulation to re-evaluate the safety of the use and sale of the herbicide by January 1, 2029, and determine whether to renew its registration or create new restrictions. The bill was signed into law by Governor Gavin Newsom on September 27, 2024.

“We are encouraged by the progress being made in California setting the example for other states to act when it comes to evaluating the safety and toxicity of chemicals with long term neurological and other health implications,” said Julia Pitcher, MJFF's director of state government relations.

New This Year: Funding Parkinson's Research

This year, MJFF embarked on a new effort to secure state funding for Parkinson's research in California, Connecticut, Illinois and Pennsylvania. In June, MJFF joined Pennsylvania state representative Kyle Mullins to announce his intent to seek $10 million in the state's budget to fund research on neurodegenerative diseases including Parkinson’s, ALS and Alzheimer’s.

With the help of local advocates, we were able to secure a starter fund of $3 million in Pennsylvania. This is the first time a state has ever dedicated general fund dollars for Parkinson’s research in the history of MJFF’s public policy efforts. The State Policy team plans to continue to build on this success in other states in 2025.  

Inspired? Act Now!

Join our Parkinson’s Policy Network to get access to opportunities to advocate for policy change to accelerate science, expand access to care and improve everyday life for people living with Parkinson’s in your state now, and in the future.