So… your friend has Parkinson’s.

Harrison Ford and Michael J. Fox share advice on how best to be there for someone with Parkinson’s, from navigating changes in handwriting to staying connected and helping counter social isolation.

Learn more about how you can help find a cure website. bit.ly/4xuz8M4

Momentum is building: On June 18, Representatives Anna Paulina Luna (@repluna) and Chellie Pingree (@chelliepingree) introduced the Paraquat Prevention Act. This significant milestone reflects a growing recognition among lawmakers that paraquat poses a public health concern that tion.

We spoke with Dan Feehan, MJFF’s chief policy and government affairs officer on where efforts to ban paraquat stand, what’s happening at the state and federal levels and how advocacy is helping drive change.

Read more: michaeljfox.org/news/how-close…

Today, @GovPhilScott signed H. 739 into law, making Vermont the first in the United States to ban paraquat, a pesticide linked to increased Parkinson’s disease risk.

Upon signing the bill, Governor Scott said: “Today, I signed H.739, which phases out the use of the harmful the coming years. I appreciate Michael J. Fox and his Foundation for their work on this issue and hope this can serve as a model for other states to follow.”

Next, Vermont will end the sale and use of paraquat later this year, with a phased transition for certain crops until a full statewide ban takes effect in December 2030.

70+ countries and one U.S. state have now banned paraquat. This is a clear and critical message to other states and our federal government: The time to ban paraquat is now.

This week, Vermont lawmakers passed bipartisan legislation to ban paraquat — and with the Governor’s signature, Vermont will become the first state in the U.S. to address this environmental risk linked to Parkinson’s disease.

Every step of the way, advocates raised their voices, s and pushed for change — and it resulted in a major victory for the Parkinson’s community.

Vermont’s actions send a clear and critical message to other states and our federal government: the time to ban paraquat is now.

Read more in our latest article about this historic milestone and how you can bring this change to your state. michaeljfox.org/news/vermont-p…

Today’s House vote was a critical win for public health and the Parkinson’s community. By passing the Luna Amendment, Congress removed harmful language from the Farm Bill that could have blocked states from adopting stronger pesticide protections — including efforts to ban ke paraquat. We’re grateful to @RepLuna and all who voted to protect the public good.

Lawmakers need to hear from people impacted by paraquat — a pesticide linked to Parkinson’s disease.

The federal government is paying attention, but attention isn’t enough. More than 70 countries have banned paraquat, including the EU and China. The U.S. has not.

If you or a ion to paraquat or other environmental exposures, your story can help drive urgent action. 🔗 michaeljfox.org/advocacystory?…

As Congress looks at @NIH funding, The Michael J. Fox Foundation stands united with @APDAParkinsons & @ParkinsonDotOrg to say robust investment in research is essential. #FundNIH #Act4PD

MJFF + our over 2.75 million friends and advocates across America thank you, @SenSchumer, for your tremendous leadership in passing the National Plan to End Parkinson’s. Let’s get to work!

For @RaceTrac, its legacy of giving to Parkinson’s research is personal. Through their annual Run for Research 5K and opportunities in-store, RaceTrac has raised over $7 million for MJFF research programs. Learn more from @kristiwooten’s piece in @gpbnews. bit.ly/3PyxHaU

Recent findings announced in August reveal a genetic variant that appears to increase the risk of #Parkinsons disease among people of African descent. In a recent article from @NPR, managing director of @ASAP_Research, Ekemini Riley, PhD discusses the significance of this ons for the future of Parkinson’s research and therapies.

Read more: bit.ly/48oRZfD

"In celebration of Hispanic Heritage Month, we recognize that diversity is the foundation of MJFF’s strength. It is through the blend of experiences, perspectives, and ideas that we expand the frontiers of Parkinson’s research." - Vanessa Arnedo, MJFF Chief People Officer

Please join us in congratulating our founder, @realmikefox, as the recipient of the 2023 Elevate Prize Catalyst Award conferred by the @ElevatePrize. The award recognizes prominent individuals who use their influence to inspire social action.

Recognized for his tireless optimism to change the future for millions of people and families in the Parkinson’s community, Michael was presented the award onstage last night at #CGI2023.

bit.ly/45Zefe6

A #Parkinsons diagnosis can bring many questions and emotions. In our upcoming webinar on September 21 at 12 p.m. ET, expert panelists will discuss ways to manage emotions and navigate the early years of a Parkinson’s diagnosis.
Register now: bit.ly/3PeAHJc

Over the last three days, The Michael J. Fox Foundation has been on a mission to raise funds for critical research that still needs funding. We want to thank our devoted community during these three days of action. With your support, we are closer to a world without Parkinson's.

Our biomarker breakthrough is a direct result of the progress we have made with the help of our supporters. Help us ensure that time-sensitive research projects get the necessary resources in 2023 to find the next breakthrough in #ParkinsonsDisease. ➡️ bit.ly/3LnrxsJ

During the next three days, The Michael J. Fox Foundation is on a mission to raise funds for research that still needs funding. Support our efforts today for a better tomorrow. 👇 bit.ly/461mvut

*Please click on the video in order to pause it for more reading time*

There are only 5 days left of National Make-A-Will Month. If you haven't created or updated your will, your future wishes may not be protected. Get tips on how and when to create/update your will with our "17 Reasons to Update Your Will" guide today. bit.ly/3OUqyky

Until recently, our understanding of Parkinson’s biology has been limited to mainly volunteers of European descent. In a groundbreaking research discovery, today new findings published in @TheLancetNeuro reveal a novel genetic variant that increases the risk of Parkinson's among nt. This finding — enabled by support from the @ASAP_Research initiative and The Michael J. Fox Foundation — importantly provides a step toward therapeutic development and research that is reflective of the diverse biology and experiences of all individuals living with Parkinson's.

Learn more: bit.ly/3E82RAz

Join us for our State of the States webinar next week August 30th at 12 p.m. ET as we discuss our Parkinson's policy #legislative wins, losses, and lessons learned along the way in state legislatures across the U.S. Register today: bit.ly/3YydSo5

Read our latest blog to learn more about Allie's research journey in our landmark study and how her involvement early on in her diagnosis is playing a critical role in how we understand and treat the disease. bit.ly/44yib4l

Join us on October 29 as we run, walk, and rally together against Parkinson’s. Participants will have the liberty of choosing between 1-Mile or 5K with a chance to win exciting prizes for the top fundraisers.

Lace up and register today: bit.ly/3QMRLrZ

Today is #NationalNonprofitDay, and we want to take a moment to express our deepest gratitude to our worldwide community of supporters. Your generosity, dedication, and unwavering commitment have helped us accomplish so much in pursuit of a cure for #Parkinsons. Thank you for and every year.

Stem cells have grabbed headlines for decades. Now, at last, they are starting to deliver on their therapeutic promise, with multiple stem cell therapies in clinical trials for #Parkinsons disease.

In this episode of our award-winning “Parkinson’s Science POV” series, experts potential of stem cells for Parkinson’s disease and the latest #research in the field.

Listen to the full episode here: bit.ly/3E0zfoK

This episode was brought to you in partnership with @BlueRockTx

Meet Mona, a monthly supporter of The Michael J. Fox Foundation (MJFF). Diagnosed with Parkinson's in 2017, Mona has ensured that her impact on Parkinson's research will last forever by including MJFF in her will.
Read more: bit.ly/3s0jwTE

Smell loss may be one of the most important signals of #Parkinsons risk. Our landmark study is exploring this link. If you're age 60 and older without Parkinson's, you can help this research by taking a free scratch-and-sniff test. Request yours today at mysmelltest.org/getmytest.

Join us in Seattle, Washington on September 9, and Columbus, Ohio on October 14 for PDIQ, our free educational event designed for people with Parkinson’s and their loved ones. ​

Discover new research and network with the local Parkinson's community: bit.ly/3KzedkK

The Michael J. Fox Foundation enjoyed meeting thousands of new and old friends in the Parkinson’s community for the 6th @WorldPDCongress (WPC) in Barcelona, Spain last month. See a few of our favorite behind-the-scenes highlights at #WPC2023!

"Off" is a term doctors and researchers use frequently in Parkinson's care. But people with PD may be less familiar with the term or what it means for them. In our webinar replay, we cover tips for managing “off” time and the latest research. Register now: bit.ly/45fdooS

We hear it all the time, whether we have Parkinson’s disease or not: Eat a healthy, balanced diet. But what does that mean? What’s healthy and what’s balanced?

Learn more in our Ask the MD video, Dishing on Diet for Parkinson’s: bit.ly/3OiUvKV

More than 60% of U.S. adults have not created a will. At The Michael J. Fox Foundation, we're aware of how daunting making a will can be, but it doesn't have to be.

Download our free and easy to use guide to ensure you leave a lasting legacy. 👉 bit.ly/3DIMFp2

Come one, come all to the Denver Run/Walk on October 8 at City Park Pavilion! 🏃 🏃‍♀️

Help us raise awareness and funds for Parkinson's research, one step at a time. Together, we can make a significant impact on the lives of millions. Register now: bit.ly/45beJNx

The Michael J. Fox Foundation mourns the passing of Patient Council member Bill Wilkins.

Founder of the Wilkin’s Parkinson’s Foundation, Bill is remembered as an extraordinary person, leaving a lasting legacy in Parkinson’s research.

Full tribute: bit.ly/43R6WTT

What exactly is gene therapy and how does it work? Who is a candidate for gene therapy? When might we see a gene therapy for Parkinson’s disease?

Learn more from our recent podcast, brought to you with support from Asklepios BioPharmaceutical, Inc. (@ask_bio).

Our latest film highlights the achievements that have been fueled by our extraordinary community. From the first large-scale genetic map of #Parkinsons to this year’s landmark biomarker discovery, none of this would’ve been possible without your help. bit.ly/3Oxb07D

This #WorldBrainDay, take a significant step towards understanding and improving brain health with our free guide. Explore tips for supporting brain health at every age, your role in research, and how to reduce the risk of brain diseases like #Parkinsons. bit.ly/3WC19Ox

REM sleep behavior disorder (RBD) can be an early indicator of Parkinson's disease. Dr. Stephen Joza discusses the connection and the critical role people with RBD play in research.

Listen to the full podcast episode to learn more: bit.ly/46VGY4H

With the help of our supporters, we announced 61 grants totaling more than $13.7 million in April and May of this year.

Help us maintain this momentum by donating today: bit.ly/46VNQz1

Calling all Denver Runners + Walkers!

Join us on October 8, 2023, for the #MJFF's annual Denver Run/Walk. Unite with runners and walkers worldwide to help move a cure for Parkinson's disease over the finish line.

Register to raise awareness for #PD: bit.ly/44rpCuA

Ends soon! Register for MJFF's PD Therapeutics Conference with early bird special promo code EB2023. Join over 300 research and business development professionals in NYC for the world's only conference exclusively focused on PD drug development. Learn more bit.ly/44lehfC

Join us on August 26 to be part of a global community uniting to pedal toward a cure for Parkinson's disease.

Can't participate in Tour de Fox? Discover more ways to give to the MFJJ this summer bit.ly/3XT60xi

In our upcoming webinar, expert panelists will discuss how genes play a role in #Parkinsons, how gene therapy might treat disease, and more.

This webinar is brought to you with support from Asklepios BioPharmaceutical, Inc. (@ask_bio).

Register now: bit.ly/3XxDKzN

Parkinson's IQ + You is coming to Seattle, Washington on September 9, 2023! Join us for an empowering day of learning and networking with fellow Parkinson's advocates.

Register now: bit.ly/3O6A3hr

Did you know there are more ways to get involved besides direct financial donations? Discover the different ways to further support Parkinson's research ➡️ bit.ly/449qRi1

Our study is exploring the connection between long-term smell loss and risk for Parkinson’s. If you are age 60 and up without Parkinson’s, you can help this critical research by taking a free scratch-and-sniff test. Request yours today at mysmelltest.org/getmytest.

There are many ways you can support our mission of finding a cure for Parkinson's disease. Your support will ensure the development of improved therapies for those living with Parkinson's today.

Discover which gift option works best for you 👉 bit.ly/3NneEz3

Our Legacy Circle was founded to thank and honor those who have named us in their estate plans.
Help ensure Parkinson's research can continue for years to come by joining our Legacy Circle.

Is MJFF already part of your future plans? Let us know today: bit.ly/3NJGOWv

When you give to The Michael J. Fox Foundation, you help us make a difference.

Discover the different gift options available to you and we'll work with you to find a charitable plan that lets you provide for your family and support Parkinson's research. bit.ly/3NEFrZ6

Planned Giving is a way of giving that allows everyone to incorporate causes they care about into their financial and estate plans, but why is it important for you?

Get started here ➡️ bit.ly/46jdmh6