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Bills · 2019-2020 Regular Session

SB 908

Died at session end Official bill text Atom feed

Relating to: information on Down syndrome. (FE)

Family Genetics and genetic testing Guardian and ward Health services department of — Health Medical service — Occupations Nurses Organization miscellaneous Physician

  1. Introduced, stopped here
  2. Passes Senate, not reached
  3. Passes Assembly, not reached
  4. Governor signs, not reached
  5. Law, not reached

Unfamiliar terms? Glossary

What this bill does

Plain-language analysis by the nonpartisan Legislative Reference Bureau

This bill requires certain health care practitioners and genetic counselors who

provide prenatal or postnatal care or genetic counseling, who administer or request

administration of prenatal or postnatal screening or diagnostic tests that detect

Down syndrome, and who receive the results of those tests to deliver certain

information to an expectant parent, parent, or guardian whose child has a prenatal

screening that indicates or a postnatal diagnosis of Down syndrome. The bill

requires the Department of Health Services to make available the information

related to Down syndrome specified in the bill in informational support packages and

on its Internet site. The bill also requires DHS to establish a grant program to award

grants to at least one nonprofit organization for the creation of the information

materials on Down syndrome specified in the bill.

Sponsors

Introduced by: Kooyenga (R)

Full history

  1. Mar 26, 2020 · Senate

    Introduced by Senator Kooyenga

  2. Mar 26, 2020 · Senate

    Read first time and referred to Committee on Health and Human Services

  3. Apr 1, 2020 · Senate

    Failed to pass pursuant to Senate Joint Resolution 1