Designates March 28, 2015, as Prader-Willi Syndrome Day in Lousiana in honor of Cooper McReynolds.
The resolution does not impose any new laws or regulations but serves to raise awareness and recognition of Prader-Willi Syndrome, highlighting the impact of this disorder on individuals and families. By officially designating a day for PWS, it is part of broader efforts to inform the public about the disorder, which includes intellectual impairments and serious health issues like chronic overeating and diabetes. It also seeks to promote necessary educational resources and services for those affected by the syndrome and their caregivers.
SCR111 is a Senate Concurrent Resolution designating March 28, 2015, as 'Prader-Willi Syndrome Day' in Louisiana. This resolution honors Cooper McReynolds, a representative of those affected by Prader-Willi Syndrome (PWS), which is a congenital genetic disorder. PWS affects an estimated one in thirty thousand individuals globally, including approximately thirty children currently diagnosed in Louisiana. By establishing this day, the resolution aims to promote awareness of the challenges faced by those living with this condition and the need for public understanding and support.
The sentiment surrounding SCR111 is generally positive, reflecting a collaborative effort among legislators to acknowledge and support individuals with rare diseases. The designation of a specific day for PWS serves as a rallying point for advocacy and community support, creating an opportunity for education and compassion toward those affected. Overall, the resolution highlights the importance of understanding rare genetic disorders in Louisiana and fostering a supportive environment for individuals with such conditions.
There were no significant points of contention reported surrounding SCR111, as it was overwhelmingly supported in the Senate with a unanimous vote of 34-0. The resolution is seen as a non-controversial measure, focusing on raising awareness and not involving debates over policy or funding. However, it emphasizes the ongoing need for advocacy for individuals with rare diseases and the importance of continued legislative support for health-related awareness initiatives.