The CurePSP Center of Care network was established in 2017 with the goal of connecting people diagnosed with progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) or multiple system atrophy (MSA) to the best possible clinical care to support their disease management and quality of life. Medical centers have been designated a CurePSP Center of Care through eligibility criteria centered around leadership in specialized therapies and treatment options, comprehensive support services and clinical research dedicated to PSP, CBD and MSA. There are currently 32 CurePSP Centers of Care in the United States and 4 in Canada, and CurePSP aims to expand this foundational care network in the coming years.
Comprehensive Care
Improving diagnosis, treatment and support for rare neurodegenerative diseases
Leadership
Supporting the PSP, CBD and MSA community through regional leadership, outreach and resource sharing
Awareness
Serving as advocates and educators for patients, families, healthcare professionals and policymakers
Collaboration
Partnering with CurePSP and the Center of Care network to enhance care and research
Mission of the CurePSP Centers of Care Program:
- Enhance access to accurate and early diagnosis, high-quality and state-of-the-art clinical care, and comprehensive support for PSP, CBD and MSA.
- Serve as regional leaders and resources for those affected by PSP, CBD and MSA and healthcare professionals.
- Increase awareness of PSP, CBD and MSA among patients, families, healthcare professionals, policymakers, and local and larger communities.
- Promote collaboration within the CoC network to optimize standards of care delivery for PSP, CBD and MSA and to create opportunities for multi-center research initiatives.
Centers of Care Listing
Please see this document for the full list of CurePSP Centers of Care.
CARES Grants
The CurePSP Collaborative Approaches to Resources, Education and Support (CARES) grant program was launched in 2022 to foster partnerships within the center network through a shared goal of understanding and addressing the unmet care needs of the atypical Parkinsonism community.
CARES projects must:
- Involve at least two CurePSP Centers of Care
- Focus on one or more of the following areas relating to PSP, CBD and/or MSA:
- Evaluating ways to enhance access to care (e.g., waiting times, telehealth)
- Assessing gaps and addressing improvement in support and outreach for underserved or underrepresented populations (e.g., racial, ethnic or gender differences in lived experiences, health literacy, rural or isolated communities, LGBTQ+)
- Studying the provision of novel person-/family-centered diagnostics, individualized goals of care, skill-building programs, or rehabilitative, mental health or palliative care services
- Educating the medical community in best practices in diagnosis, assessment and treatment
- Attending to other relevant high priority needs identified by the Centers of Care
- Be designed to produce measurable, generalizable and publishable data
Best Practices in the Clinical Management of Progressive Supranuclear Palsy and Corticobasal Syndrome
In 2021, the CurePSP Center of Care network published a consensus statement on the pharmacological and multidisciplinary management of PSP and CBS in the prestigious peer-reviewed journal, Frontiers in Neurology.
For Healthcare Professionals
See criteria for CurePSP Center of Care designation here.
For questions related to applying for Center of Care designation, please email Jessica Shurer, MSW, LCSW, Director of Clinical Affairs and Advocacy, at shurer@curepsp.org
Visit our webpage for healthcare professionals for additional resources, including how to order educational materials for your clinic, continuing education opportunities, scientific publications and a differential diagnosis tool.