Louisiana Senate Bill SR3

Louisiana 2015 Regular Session

• Introduced: 4/13/15
• Passed: 4/14/15

Caption

Commends Tara MacInnes for her tireless works with Moyamoya disease and recognizes May 6, 2015, as Moyamoya Disease Awareness Day.

Impact

The resolution solidifies Moyamoya Disease Awareness Day in Louisiana, which is an important step in increasing public knowledge about this rare disease. It brings attention to the struggles faced by individuals diagnosed with Moyamoya disease and highlights the need for supporting patients and their families. This increased awareness may influence healthcare policies and encourage funding for research and treatment options.

Summary

Senate Resolution No. 3 pertains to the commendation of Tara MacInnes for her significant contributions to promoting awareness of Moyamoya disease. Moyamoya disease is a rare cerebrovascular disorder characterized by the narrowing of arteries at the base of the brain, which can lead to serious health complications such as strokes. The resolution recognizes May 6, 2015, as Moyamoya Disease Awareness Day in Louisiana, highlighting the importance of awareness and advocacy for those affected by this condition.

Sentiment

The sentiment surrounding SR3 is largely positive, reflecting a supportive recognition of Tara MacInnes's efforts and the broader issue of rare disease advocacy. The bill emphasizes community awareness and solidarity among those affected by Moyamoya disease, contributing to a sense of unity and hope for patients and their families.

Contention

While SR3 is generally well-received, as it simply honors an individual and proclaims a day for awareness, there are underlying challenges in terms of resources and recognition for rare diseases like Moyamoya. The bill does not directly address funding or specific initiatives but serves as a platform to promote discussions about the necessity of better treatment and support for patients.