California 2017-2018 Regular Session

California Senate Bill SR108

Introduced
4/30/18  
Refer
4/30/18  
Refer
4/30/18  
Passed
5/7/18  

Caption

Relative to Cystic Fibrosis Awareness Month

Impact

The passing of SR 108 has a primarily symbolic impact but seeks to encourage state agencies and healthcare professionals to advocate for enhanced support for those with cystic fibrosis. By promoting awareness, the resolution aims to stimulate interest in research and development for potential treatments and highlights the urgency of addressing the needs of a community that continues to face significant health challenges due to the disease.

Summary

Senate Resolution No. 108, introduced by Senator Monning, designates May 2018 as Cystic Fibrosis Awareness Month in California. The resolution aims to raise public awareness about cystic fibrosis, a severe genetic disease that affects approximately 30,000 individuals in the United States. The bill emphasizes the importance of education regarding the disease, its symptoms, and the need for early diagnosis to improve the lives of those affected. It also highlights significant advancements in the understanding and treatment of cystic fibrosis, which have led to increased life expectancy for patients.

Sentiment

The sentiment surrounding SR 108 is notably positive, reflecting a collective commitment to improving awareness and support for individuals with cystic fibrosis. Legislators and advocates alike view the resolution as an essential step in mobilizing public and institutional support for continued research and better care options. The recognition of Cystic Fibrosis Awareness Month is seen as a critical effort to acknowledge the struggles of patients and their families, thereby fostering a more informed and compassionate society.

Contention

There seems to be little contention associated with the resolution itself, as it focuses on raising awareness rather than being transformative legislation. However, it does underline ongoing discussions about the adequacy of healthcare resources and research funding for rare genetic diseases. Some advocates may argue for more immediate legislative actions targeting healthcare improvements and direct support systems for patients, yet SR 108 serves as a platform for broader discussions on these vital issues.

Companion Bills

No companion bills found.

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