HUGE thank you to @RepWexton for your continued collaboration and awareness-raising and @InsidePolitics for telling her story and featuring @CurePSP 📣🧠
EXCLUSIVE: "When it comes to illness, progressive is not a good thing to be." Virginia's @RepWexton will retire next year as she battles a rare brain disease described as "Parkinson's on steroids." She shares her story with @MZanona in a sit-down interview. #InsidePolitics
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
#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.
I was in Sterling today to celebrate how our Bipartisan Infrastructure Law is making it possible to clean up the Hidden Lane Superfund site.
I applaud @EPA and local govt efforts to clean up toxins and restore clean drinking water. We're making our community safer and healthier.
🌟Join us for an insightful webinar on advocacy and the bipartisan National Plan to End Parkinson's Act! Learn how @CurePSP and @MichaelJFoxOrg collaborate to drive this crucial legislation forward and how you can get involved! Register now: https://t.co/76ickscN4u
Thrilled to connect with our partners at #AANAM! These connections are the driving force behind our mission. Partnership propels progress. @MissionMSA@ParkinsonDotOrg@AFTDHope
The @ParkinsonDotOrg Team Training and Advanced Team Training will be held in Minneapolis this year! @CurePSP is partnering with the Parkinson Foundation for the Advanced interdisciplinary course focused on atypical Parkinsonian syndromes. Join me!!
https://t.co/Oy0PuU8LJr
Harness the power of education with our CurePSP Toolkit! Perfect for healthcare, academic and community leaders looking to make a difference. Last reminder! Secure your #CurePSP Awareness Toolkit today!❤️https://t.co/WuGXyZjaNu
#HopeInAction#Awareness#NonProfit#Advocacy
Always an honor to meet the most influential disease advocacy groups for neurodegenerative diseases on the planet. Thank you for your work 🙏🏼
#AAN2024@CurePSP@AFTDHope@alzassociation
Excited to see our Associate Director, Courtney Malburg, attending the session on "Neuro-Palliative Care: Maximizing Quality of Life in Serious Neurologic Illness" at #AANAM! Maximizing quality of life is crucial for patient well-being.
For a few days, half of @CurePSP is meeting in our New York offices. I snuck in during one of their work sessions. The Clinical Affairs & Advocacy team is working with the Marketing and Communications team to plan several exciting efforts. After a long day, they are all smiling!
Exciting visit to @PDCMDC, our newest #CurePSP Center of Care! 🏥 @RoyCLinMD and Rory Mahabir led a dynamic agenda featuring breakthrough clinical services, research insights and a peek into neurodegenerative disease studies in fruit fly models. Thank you for your dedication!
We're proud to announce the recipients of CurePSP's Collaborative Approaches to Resources, Education, and Support (CARES) Grants for 2023, marking the second year of this impactful funding program. 🌐
Continue Reading: https://t.co/oqnbI3Kbrv
Grateful for the tireless advocacy of @RepWexton whose dedication to the Parkinsonism community has resulted in the House’s passage of this historic legislation. This is huge for the @CurePSP community. Now we must continue the momentum on the Senate side! 📣
🚨 The House just passed the bipartisan National Plan to End Parkinson’s Act! 🚨
This is a transformative step to fight PD & atypical PD diseases like mine. We’re going to save lives and give families hope.
I’m grateful to @RepGusBilirakis & @RepPaulTonko for their leadership.
Thank you @MacFarlaneNews for helping amplify @RepWexton voice and willingness to tell her story and struggles living with PSP. Thank you for working with her to raise awareness. It makes a huge difference for all aspect of what we’re trying to solve.
It was a great pleasure to attend @CurePSP Hope as big as Texas at Dallas, meet the community, and present what @BCMhouston@BCMneurology@PDCMDC has to offer.
Thanks @JoriFleisher for the compassionate talk and @JessicaShurer for your innovative and exemplary leadership!
We are extremely fortunate to have @CurePSP Center of Care directors @RoyCLinMD and @JoriFleisher representing at our Hope As Big As Texas event to benefit the CurePSP Quality of Life Respite Grants.
Patients with #PSP need to be sooner and more frequently. ⚡️Senior author⚡️on an important POV manuscript with Marian Dale of @OHSUBrain, @FarwaAli_, @KristopheDiaz and many others from @CurePSP Centers of Care. Out now in @ParkinsonismD! https://t.co/z5d51uEdaU
Successful North Carolina visit! Productive discussions with Dr. Sklerov at the #CurePSP Center of Care at @UNCneurology on PSP trials and legislative advocacy on insurance coverage while also connecting with some incredible families! A united front for a stronger community. 🌟
📢 Exciting news from #CurePSP! We've expanded our network to 33 specialized medical centers across the US and Canada with the addition of @PDCMDC, @VanderbiltU and @univmiami. Together, we're advancing care for PSP, CBD and MSA. 🌎
https://t.co/RS2byTY1p1
#BecauseHopeMatters