Bill > SR13

This state Senate resolution addresses Stiff Person Syndrome (SPS), a rare neurological autoimmune disorder affecting approximately one in a million people, by raising public awareness and supporting research efforts. The resolution acknowledges that SPS is a terminal condition with no known cure, predominantly affecting females and causing significant physical and social challenges such as muscle stiffness, spasms, and impaired mobility that often lead to social isolation. The Senate formally supports educating the public about SPS, applauds advocates and organizations working to promote research and provide support, and recognizes the commitment of researchers and health professionals seeking effective treatments. Additionally, the resolution designates March 15, 2025, as International Stiff Person Syndrome Awareness Day in California, aiming to highlight the syndrome's impact and encourage greater understanding among medical professionals and the general public. The resolution emphasizes the importance of early diagnosis, continued research, and providing hope and support for individuals affected by this challenging condition.

https://leginfo.legislature.ca.gov/faces/billStatusClient.xhtml?bill_id=202520260SR13