Top Tweets for #PSPAwareness
Progressive supranuclear palsy is often mistaken for other conditions. The sooner the real culprit is discovered, the sooner the right course of treatment can begin: https://t.co/iusRlT6wTv
#PSPawareness #BrainHealth
The Florida Senate has declared May 2026 as PSP Awareness Month. What does this mean—and why is it important? Learn more in the graphic, then visit the Fixel Institute website to explore our PSP Center of Excellence and FAQs.
#PSPAwareness #NeurodegenerativeDiseases #Advocacy
After progressive supranuclear palsy left her unable to talk, former Rep. Jennifer Wexton found her voice again thanks to assistive technology.
Read how she's using it to raise awareness and inspire others like her: https://t.co/HwMS9GxAKd
@RepWexton #PSPawareness #Dementia
Progressive Supranuclear Palsy (PSP) is a rare condition causing movement issues & dementia, often misdiagnosed as Parkinson’s. Symptoms include balance problems, eye movement difficulties, & cognitive decline.
#PSPAwareness #Dementia #RareDisease
It’s day 9 of our 12 Days of Awareness 🎄🎅. We’re sharing the Personal Experiences of PSP, like Claire, who details the journey her family went through when her Mum began experiencing PSP symptoms. Read Claire’s story in full here: https://t.co/ayATjMhKHj #PSPawareness
‘#PSP is rare but real.’ 💙 This inspiring lady raises awareness of Progressive Supranuclear Palsy on World Movement Disorders Day. Recognizing early symptoms is key. Let’s break the stigma & support each other! #PSPAwareness #BreakingTheStigma #MoveDisorder
@movedisorder
Louis, Aric, Miranda, Liam, & Florence are leaving Newquay to climb each of Ben Nevis, Scafell Pike & Snowdon in 24 hours to raise awareness & funds for the @PSPAssociation.
Florence joined @twhowe_media to explain more: https://t.co/6JSHiHa7YB
#KeepItCHAOS #PSPAwareness
PSP is a neurological disorder that impacts 30,000 folks across the country – including my friend @RepWexton – yet there is no known cure.
This #PSPAwareness Month, I’m working to help people better understand what PSP is and fight so that no one has to live with this disease.
What a week! Started with the @BrainEnviro, then a congressional briefing on #PSPAwareness with @RepWexton and @MichaelJFoxOrg, and ending with the passing of the National Plan to End #Parkinson’s Act. Amazing advocacy, collaboration and progress all around! 🧠📣
BREAKING: The U.S. Senate unanimously passed the National Plan to End Parkinson’s Act! The passage caps off a historic week of advocacy for CurePSP that came to fruition after years of dedicated support from the entire CurePSP community. #HR2365 Full story:https://t.co/jZ0r976HTv
Showing my support today for my good friend, @RepWexton, this #PSPAwareness Month. PSP is a neurological disorder that impacts 30,000 Americans—yet there is still no known cure. We must do more to better diagnose, treat, and cure PSP. It's on all of us to step up.
PSP & CBD Awareness Week is fast approaching - 17 to 23 June.
We will launch a new campaign called #WeCare. Learn more: https://t.co/vDR2TD5Dsu
We encourage you to help us raise as much awareness of PSP & CBD as possible.
#PSPAwareness #CBDAwareness #RaiseAwareness #PSP #CBD
Today I'm sharing my support for #PSPAwareness Month and the urgent need to better diagnose, treat, and cure PSP.
This "Parkinson's on steroids" condition is devastating for families across the country and we must do more to fight this disease.
PSP or "Parkinson's on steroids" impacts 30,000 Americans, including my friend @RepWexton who I've worked with to promote STEM education & stop the CCP's forced labor.
During #PSPAwareness Month, we help people better understand this devastating disease & fight for a cure.
Today I'm sharing my support for #PSPAwareness Month & the urgent need to better diagnose, treat, & cure PSP. This "Parkinson's on steroids" condition is devastating for families in Georgia & thousands more across the country.
I am inspired by @RepWexton & proud to join her.
PSP has taken a toll on my body, but it has not affected who I am inside nor my dedication to doing my job of serving my community in Congress.
I'm leading #PSPAwarenessWeek to make the most of my platform and spread the word so we can better fight this devastating disease.
Today I'm sharing my support for Progressive Supranuclear Palsy (PSP) Month and the urgent need to better diagnose, treat, and cure PSP. #PSPAwareness
PSP is a neurological disorder that impacts 30,000 Americans – yet there is no known cure.
This #PSPAwareness Month, I’m joining @RepWexton to raise awareness and fight for more resources so that no one has to live with this devastating disease.
PSP has taken a toll on my body, but it has not affected who I am inside nor my dedication to doing my job of serving my community in Congress.
I'm leading #PSPAwarenessWeek to make the most of my platform and spread the word so we can better fight this devastating disease.
PSP is a neurological disorder that impacts 30,000 Americans, yet there is no known cure.
This #PSPAwareness Month, we're working to help people better understand what PSP is and fight so that no one has to live with this devastating disease.
Thank you Rep. Carter for your support! Sharing information that spreads #PSPAwareness is crucial to expanding research and care initiatives
Showing my support today for #PSPAwareness Month. PSP is a neurological disorder that affects 30,000 Americans, but there is no known cure. I’m standing with those battling this disorder and their families and we fight for more research. @CurePSP @RepWexton
I join my friend and colleague @RepWexton on #PSPAwareness Month to help people learn about PSP and advocate for better resources and research so no one has to live with this devastating disease.
Showing my support today for #PSPAwareness Month. PSP is a neurological disorder that affects 30,000 Americans, but there is no known cure. I’m standing with those battling this disorder and their families and we fight for more research. @CurePSP @RepWexton
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