Top Tweets for #PSPAwarenessMonth
May is #PSPAwarenessMonth, made even more meaningful by the Florida Senate officially designating May 2026 as Progressive Supranuclear Palsy Awareness Month. Raise awareness for this neurodegenerative disease and learn answers to 10 common PSP questions: https://t.co/wzxM539Vct
This #PSPAwarenessMonth, we’re bringing attention to progressive supranuclear palsy (PSP), a complex, rapidly progressing disease that affects movement, vision, speech, and more.
Raising awareness can help drive earlier disease recognition and advance the research needed to change what’s possible for patients.
We are deeply committed to the progressive supranuclear palsy (PSP) community during May, which is dedicated to raising awareness of this disease, and beyond.
Learn more about PSP on our website at https://t.co/m3HFvvk0bW
#PSPAwarenessMontWe are deeply committed to the progressive supranuclear palsy (PSP) community during May, which is dedicated to raising awareness of this disease, and beyond.
Learn more about PSP on our website at https://t.co/m3HFvvk0bW
#PSPAwarenessMontWe are deeply committed to the progressive supranuclear palsy (PSP) community during May, which is dedicated to raising awareness of this disease, and beyond.
Learn more about PSP on our website at https://t.co/m3HFvvk0bW
#PSPAwarenessMontWe are deeply committed to the progressive supranuclear palsy (PSP) community during May, which is dedicated to raising awareness of this disease, and beyond.
Learn more about PSP on our website at https://t.co/m3HFvvk0bW
#PSPAwarenessMontWe are deeply committed to the progressive supranuclear palsy (PSP) community during May, which is dedicated to raising awareness of this disease, and beyond.
Learn more about PSP on our website at https://t.co/m3HFvvk0bW
#PSPAwarenessMonth
This #PSPAwarenessMonth, we remember our founder Richard Rainwater, who was driven by his experience with #PSP to expand his philanthropic efforts to include research into primary tauopathies. Explore his story: https://t.co/Ngkw9J651X
It is estimated that PSP impacts more than 30,000 Americans, though the disorder is
often misdiagnosed.
Every day, @RepWexton represents her district with strength and courage every day. I am honored to call her a colleague and friend.
#PSPAwarenessMonth
As we mark #PSPAwarenessMonth, let's honor the tens of thousands of Americans affected by Progressive Supranuclear Palsy. I stand with @RepWexton in her courageous battle and her mission to enhance awareness, improve diagnosis and treatment, and ultimately find a cure for PSP.
BIG NEWS: The Senate just took a groundbreaking step to fight Parkinson’s and related diseases like my PSP.
Passing this bipartisan bill, which I’ve championed in Congress, gives families like mine hope that one day soon we can and will find a cure for these terrible diseases.
Great success of the 1st PSP Day today at @hospitalclinic with clinical, biomarker & care results of the PSP Barcelona Registry by our fab multidisciplinary team. Inspiring interaction with PSP patients & carers. Look forward to the 2nd PSP Day on May 2025!
#PSPawarenessmonth
@RepWexton has shown immeasurable strength and courage in her battle with PSP. This #PSPAwarenessMonth, I’m proud to stand with her by cosponsoring the resolution to raise awareness of this illness and recognize the individuals who battle it every day.
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.
Even while battling an unrelenting disease, my friend, constituent & Congresswoman @RepWexton continues to be an example of true public service. This Session, I carried a resolution recognizing May as #PSPAwarenessMonth in VA. Honored to join her in the fight for a #PSP cure.
Today, I'm proud to lead 100 Members in a bipartisan resolution recognizing #PSPAwarenessMonth.
I know personally how scary and devastating a disease this is for tens of thousands of Americans & their families.
It's time to step up our fight against PSP.
https://t.co/kvSc48n0jU
I stand with @repwexton in her quest to raise awareness about PSP, work to develop better treatments, & one day find a cure #pspawarenessmonth
I'm sharing my personal journey with PSP not because I want you to feel sorry for me, but because there are tens of thousands of other Americans and their loved ones fighting the same battles.
That's why I'm leading a bipartisan effort to recognize May as #PSPAwarenessMonth.
Today, I'm proud to lead 100 Members in a bipartisan resolution recognizing #PSPAwarenessMonth.
I know personally how scary and devastating a disease this is for tens of thousands of Americans & their families.
It's time to step up our fight against PSP.
https://t.co/kvSc48n0jU
Over 30,000 Americans are impacted by PSP, including my dear colleague, @RepWexton. This neurological disorder is devastating for individuals & their families, & there is still no known cure.
During #PSPAwarenessMonth, we highlight the need to better diagnose, treat, & cure PSP.
Progressive supranuclear palsy affects an estimated 30,000 Americans.
I’m wearing this hummingbird pin in support of my friend @RepWexton and the thousands fighting PSP. We must do everything in our power to combat this disease and uplift the PSP community. #PSPAwarenessMonth
#PSPAwarenessMonth recognizes the tens of thousands of Americans living with Progressive Supranuclear Palsy.
We proudly stand with our friend and colleague @RepWexton as she battles this disease and raises awareness to better diagnose, treat and finally cure PSP.
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.
Yesterday, we took part of a PSP 101 Congressional briefing with @RepWexton and @MichaelJFoxOrg. Today I’m at the @NIH @NIH_NINDS talking to leaders and funders in advocacy and neurogenetics. Two impactful days! #PSPAwarenessMonth #CurePSP
PSP is a devastating condition that @RepWexton battles every day & yet she never fails to show up & represent her constituents.
She's an inspiration & I'm proud to join her this #PSPAwarenessMonth to raise awareness & provide better care to the 30,000 people impacted by PSP.
CurePSP and Rep. Jennifer Wexton were on the Hill yesterday for a PSP Congressional Briefing! Join us in supporting her digital day of action by tagging your reps using #PSPMonth #PSPAwarenessMonth and #MyPSPStory!
Standing in solidarity with my courageous colleague @RepWexton in recognizing #PSPAwarenessMonth. Let’s help individuals battling this terrible disease in Michigan and across the U.S. receive better care and support.
My colleague @RepWexton is such a dedicated public servant, and I'm incredibly proud to stand with her as we mark #PSPAwarenessMonth.
PSP impacts 30,000 Americans—yet there is no known cure. It's time to do more to fight this 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.
This #PSPAwarenessMonth, I’m standing with my colleague @RepWexton and fighting in Congress on behalf of all Americans battling PSP. We must do more to better diagnose, treat, and cure this terrible disease.
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