We are a global alliance of people w/ Parkinson's, our partners & friends aligned to add urgency to the cause of ending PD through wellness, advocacy & research
Joined July 2020
- Tweets998
- Following543
- Followers3.2K
- Likes904
We want to hear from you.
PD Avengers Community Pulse
pdavengers.com/community-pul… is a new, ongoing way for people across the global Parkinson’s community to tell us what they are experiencing, what matters most, and where action is needed. Check it out.
#Survey #Parkinsons
Join PD Avengers for a free virtual screening of Come Talk To ME, a powerful documentary about Parkinson’s disease, speech, communication, and relationships.
kinema.com/events/Come-Talk-… #PDAvengers #ComeTalkToME #CarePartners #ParkinsonsAwareness
There is no food security without human health — and no serious brain health strategy without stronger pesticide protections.
PD Avengers is calling on the Government of Canada to clarify, constrain, and revisit Bill C-30’s pesticide amendments
Shaky C – “Soundtrack of Your Life” (Official Music Video) This is a great song released by my college pals as a fundraiser for PD Avengers. @Giffordtweet youtu.be/cWhMhXk0pm8?si=CcBw… via @YouTube
If you haven't checked out the music and video from "Shaky C" -- I encourage you to and share it widely with your friends.
shakyc.com/
It's original music and animated video. Plus, it's a fund raiser for PD Avengers.
#parkinsons #EndPD #parkinsonscouldbeyou
April is #ParkinsonsAwarenessMonth and PD Avengers & Parkinson & Movement Disorder Alliance
are raising awareness in #NYC with billboards in #TimesSquare WWW.F-PARKINSONS.COM
@SoaniaMathur @TimHagueSr @Giffordtweet @BrianGrantOrg @asoftvoicepd @MichaelOkun @RayDorseyMD
Be sure to register your sit-to-stands at standuptoparkinsons.com/ #parkinsonsawareness
Thanks @FINTECHTVglobal for having me on the closing bell show "Taking Stock" -- and for the cool graphics.
#ENDPD #WorldParkinsonsDay #SparktheNight
Spark the Night returns April 11, 2026, as landmarks worldwide light up blue to raise awareness for Parkinson’s.
Larry Gifford (@Giffordtweet) of @PdAvengers joins @JD_Durkin to discuss the mission behind the campaign and its global impact.
PD Avengers retweeted
Spark the Night returns April 11, 2026, as landmarks worldwide light up blue to raise awareness for Parkinson’s.
Larry Gifford (@Giffordtweet) of @PdAvengers joins @JD_Durkin to discuss the mission behind the campaign and its global impact.
Times Square Billboards Highlight Environmental Risks Linked to Parkinson’s einpresswire.com/article/903… @PdAvengers @PMDAlliance
Most people don’t think Parkinson’s could happen to them — until it does. #YourRiskIsReal! #Parkinson’s is the fastest-growing neurological disease. Watch. Share.
🌐 f-parkinsons.com
Thank you @PolkSheriff for spreading the word to end Parkinson's. youtube.com/clip/UgkxaYH-uHP… via @YouTube
What is the PD Avengers and how did it get started? Why are more than 10,000 people signed up as members?
parkinsonseurope.org/parkins…
April 11 is World Parkinson's Day and Spark The Night -- landmarks, bridges, buildings, and homes everywhere will glow blue for World Parkinson’s Day. You can:
✨ Light up a landmark
✨ Create a Sparklet
👉 sparkthenight.org #SparkTheNight #Sparklets #WorldParkinsonsDay
We’re asking House and Senate Labor–HHS Appropriations to make sure the National Plan to End Parkinson’s is actually implemented, not just celebrated. #whereisthePDplan
"As someone living with Parkinson’s, I know how easily communication can be misread in high-stress encounters with law enforcement. The Blue Envelope Programs Act is a way to make those encounters safer, and more respectful.” - Larry Gifford, President of PD Avengers
Today, I introduced the bipartisan Supporting Blue Envelope Programs Act with @RepRutherfordFL. Blue Envelope Programs work, in the Inland Empire and in 29 states nationwide, helping first responders communicate safely with people with Autism & I/DD. I'm excited to lead this effort to expand them nationwide.
Parkinson’s is the fastest-growing brain disease, but the National Parkinson’s Project is still invisible to patients and families. Dear Congress, #whereisthePDplan
Two years after Congress passed the National Plan to End Parkinson’s and 17 months after it became law, we still haven’t seen a public PD plan. #whereisthePDplan
Last chance!
Today we go live with DBS Explained: It’s Not Rocket Science! — a jargon-free webinar from @PdAvengers + @AbbottNews Neuromodulation.
🕙 10:00 AM PDT / 1:00 PM ET
🔗 Register: eventbrite.ca/myevent?eid=16…