# What This Bill Actually Does

This is a symbolic resolution that designates May 2024 as "Progressive Supranuclear Palsy Awareness Month." In practical terms, it's Congress saying "we recognize this disease exists and we support efforts to raise awareness about it." It doesn't create new laws, fund research, or change any government programs—it's essentially an official statement of support.

Progressive supranuclear palsy, or PSP, is a rare brain disease that affects about 30,000 Americans. It's often confused with Parkinson's disease, but it's actually a distinct condition that gets worse quickly. People with PSP experience problems with balance, speech, swallowing, thinking clearly, and vision. Most patients need full-time care within three to four years of diagnosis. There's currently no cure and no treatment that can slow the disease down.

The resolution highlights why awareness matters: PSP is frequently misdiagnosed, which delays people from getting proper care. By designating May as an awareness month, Congress is essentially giving a platform to patient advocacy groups, researchers, and families dealing with this disease to educate the public and healthcare professionals. The resolution also expresses support for continued research to find better treatments and eventually a cure. While this won't directly change your life unless you or someone you know has PSP, it signals that Congress recognizes the disease as important and supports the work of organizations fighting to help patients and their families.

Expressing support for the designation of the month of May 2024 as "Progressive Supranuclear Palsy Awareness Month".

Wexton, Jennifer

<p>This resolution expresses support for the designation of Progressive Supranuclear Palsy Awareness Month.</p>