Kentucky 2022 Regular Session

Kentucky Senate Bill SB39

Introduced
1/5/22  
Refer
1/5/22  

Caption

AN ACT relating to Down syndrome and spina bifida information.

Impact

The bill will amend the existing Kentucky Revised Statutes to formalize the obligation of health facilities and providers to distribute substantial information tailored to families receiving positive test results for Down syndrome or spina bifida. The Cabinet for Health and Family Services is tasked with creating and making available this information, ensuring its relevance and accuracy. This legislative change is expected to positively impact public health by improving the informational landscape for families grappling with these diagnoses.

Summary

SB39 is a legislative act aimed at enhancing the provision of information regarding Down syndrome and spina bifida to expectant and new parents. The bill mandates that healthcare providers, including physicians and genetic counselors, supply comprehensive and up-to-date evidence-based resources whenever they deliver a positive diagnosis for these conditions. This initiative seeks to ensure that affected families receive vital information about health outcomes, support options, and treatment pathways, thereby empowering them to make informed decisions during and after prenatal care.

Sentiment

The sentiment surrounding SB39 is primarily positive, reflecting a broader commitment to supporting families with children born with significant health challenges. Stakeholders and advocates believe that the bill recognizes the critical need for accessible, high-quality information and resources. However, there can be concerns about the implementation, ensuring that the information provided is accurate and comprehensive, leading to effective support for parents.

Contention

While support for SB39 is notably strong among healthcare providers and advocacy groups for Down syndrome and spina bifida, potential contentions could arise regarding the execution of the bill's requirements. Ensuring compliance and maintaining the standard of information issuers may be challenging, especially considering the variety of health facilities involved. Further discussions might be warranted to address these potential hurdles and ensure that the intended benefits of the bill are fully realized.

Companion Bills

No companion bills found.

Previously Filed As

KY S814

Requires DOH to provide information regarding spina bifida to certain parents and families of newborns; "Levi's Law."

KY A1937

Requires DOH to provide information regarding spina bifida to certain parents and families of newborns; "Levi's Law."

KY A2665

Requires DOH to provide information regarding spina bifida to certain parents and families of newborns; "Levi's Law."

KY S1739

Requires DOH to provide information regarding spina bifida to certain parents and families of newborns; "Levi's Law."

KY HB274

Relating to information regarding spina bifida.

KY SB1032

Developmental disabilities; spina bifida.

KY SB1024

Developmental disabilities; spina bifida

KY HB2924

Relating to information regarding Down syndrome.

KY HB3374

Relating to information regarding Down syndrome.

KY HB1058

Requires the Dept. of Health and Hospitals to provide information concerning Down syndrome to healthcare providers and on its website

Similar Bills

No similar bills found.