Help Us Crush PSP.

Brothers PSP Foundation was founded in honor of a brother who is still fighting Progressive Supranuclear Palsy — a rare, relentless neurodegenerative disease that steals movement, speech, and independence.

Most people succumb to PSP within 4–8 years of diagnosis. Our brother was diagnosed in 2014 and has fought longer than anyone we know — a true survivor. We're racing to get him, and every family like ours, a treatment or a cure before this dreadful, debilitating disease claims another life.

PSP families face impossible choices: safe transportation, home modifications, specialized equipment, and travel to the few specialists who understand this disease. We were determined that no California family should face it alone.

Today we fund the research pointing toward a cure, and provide direct, practical grants so families can focus on what matters most — time together.