New Innovative Progressive Supranuclear Palsy Trial
$75 million NIH grant could lead to the first effective drugs for a condition with few treatment options.
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A PSP Society support group is a voluntary gathering of patient and/or care-partners who share common experiences related to living with a prime of life disease such as PSP, CBD or MSA. Participants offer emotional and practical support reducing the sense of isolation that is associated with rare brain diseases.
Call for emotional support if you or a loved one has recently been diagnosed, if you're feeling isolated or if you just need to vent. Leave a message and an experienced member of our team will get back to you in 48 hours or less. We've all experience living with PSP in the family.
PSP Society scientific advisors field questions of a scientific or medical nature. Sessions are open to patients, care-partners, families and community allies affected by Progressive Supranuclear Palsy (PSP), Multiple System Atrophy (MSA), Corticobasal Degeneration (CBD) or related conditions.
Find answers to questions other in your shoes have had. Everything we share is reviewed by our team of scientific advisors. Search for keywords or browse common categories to learn at your own pace. Resources and suggestions are drawn from our community of patients and care-partners and are updated monthly.
In case of emergency, carry a wallet sized information card alerting others to your condition, associated symptoms and how to be of assistance. Request your free card mailout today.
Access and download printable informational documents on PSP, CBD and MSA to keep or to share with friends, family and healthcare providers. Learn about causes, treatments, history and the role of your allied health professionals.
News & Events
News & Events
Read about upcoming events, PSP Society of Canada updates and scientific developments.
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