Support Network

Network of Support

CurePSP is here for you and your family through the journey with PSP, CBD or MSA.

Brain Donation

By donating your brain to Mayo Clinic Brain Bank in Jacksonville, Florida, supported by CurePSP, you are providing an invaluable resource to researchers for finding a cure to end PSP and CBD.

Learn more about our Brain Donation Program

Family Conferences

Among its various educational activities, CurePSP sponsors and organizes family conferences across the country, providing people with the opportunity to learn more about PSP, CBD, and MSA and to develop a sense of community. We recognize that these diseases present daily challenges for patients and families.

Learn more about Family Conferences

Request Info

CurePSP works with academia and pharmaceutical companies to facilitate human clinical trials that are essential to advancing science and developing new drugs for PSP, CBD, MSA, and related diseases.

Submit a request for information here

Bereavement Support

CurePSP has collated the latest, most up-to-date information on PSP, CBD, and MSA available, and is happy to send all material, free of charge, upon request, to the address you provide in the form below.

bereavement support resources

Centers of Care

CurePSP Centers of Care are medical centers recognized as being able to provide quality care for the specific needs of PSP and CBD patients. This allows us to provide recommendations to patients on where they might find suitable care.

Find a CurePSP Center of Care near you

Respite Services

CurePSP has created the Cherie Levien Quality of Life Fund to ease the financial burden of getting professional, in-home respite care. Our goal in developing the fund is to reduce the stress that is often experienced by caregivers.

Learn more about the Cherie Levien Quality of Life Fund

CurePSP encourages and organizes activities that foster face-to-face communication, exchange of ideas and information, and interaction for comfort and mutual benefit to group members. The groups are for caregivers, family members, friends, and people with PSP, CBD, MSA, or a related disease. There are three ways to connect.

Find the right support for you

Newly Diagnosed with PSP, CBD or MSA?

We’ve created a comprehensive checklist to aid you in navigating a recent diagnosis of PSP, CBD or MSA. Use this helpful guide to easily connect with the CurePSP community, learn how to become your own advocate and stay proactive along your journey.

Newly Diagnosed Checklist

Connect to the Community

Through our national/international support groups and regional peer support offerings, the CurePSP community is here to empower and assist you as you navigate life with PSP, CBD or MSA.

Learn about our offerings

Educational Resources

CurePSP maintains a library of educational resources, which you can download or order, to offer guidance and tools for life with PSP, CBD or MSA.

See our full catalogue of available resources

CurePSP Centers of Care

The CurePSP Centers of Care program is a network of medical centers, 31 in the US and 2 in Canada, dedicated to the comprehensive care of PSP, CBD and MSA.

Find specialized care here

Upcoming Events

From family conferences to educational webinars to fundraisers, CurePSP hosts a variety of events to support our community and our cause.

See our events calendar here

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