This bill establishes November 12, 2025, as Creutzfeldt-Jakob Disease (CJD) Awareness Day to raise public awareness about this rare and fatal brain disorder.
David Valadao
Representative
CA-22
This bill officially establishes November 12, 2025, as Creutzfeldt-Jakob Disease (CJD) Awareness Day. The purpose is to raise public awareness about this rare, rapidly progressive, and fatal brain disorder. The House of Representatives supports this day to recognize the unique challenges faced by CJD patients and their families.
If you’re like most people, you probably haven’t spent much time thinking about Creutzfeldt-Jakob Disease, or CJD. It’s a rare, devastating, and rapidly progressive brain disorder caused by prions—abnormal proteins that mess up the brain. This resolution sets aside November 12, 2025, as Creutzfeldt-Jakob Disease (CJD) Awareness Day, specifically to shine a light on this condition and the heavy burden it places on patients and their families. It’s a purely symbolic move, but one that aims to get this rare disease on the public radar.
This resolution is about recognition, not regulation. It doesn't allocate funding, change healthcare law, or create a new agency. Instead, the House of Representatives is officially throwing its support behind the goals and ideals of CJD Awareness Day. Think of it as Congress using its platform to say, “Hey, this is a serious issue that deserves attention.” For the community of patients and caregivers dealing with this disease, this kind of official recognition can be huge, providing validation and potentially spurring greater public interest or research focus down the line.
Since this bill is a resolution establishing an awareness day, its impact is indirect. It won’t change your taxes, your commute, or your health insurance premiums. The real effect is on public knowledge. CJD is often misunderstood or completely unknown outside of medical circles. By designating a specific day, the resolution provides a focal point for advocacy groups to share information, educate the public, and push for more research into diagnosis and treatment—a critical step, given the disease’s fatal nature.
For the average person, this is an opportunity to learn about a rare disease that often flies under the radar. For those families already navigating the immense challenges of CJD, this designation is a moment of visibility, acknowledging the unique difficulties they face due to the disease's swift progression. Ultimately, this resolution is a straightforward, low-vagueness gesture of support, using the power of the calendar to bring a serious health issue out of the shadows.