Did not become law. It stopped in the Senate on May 21, 2018. The 2018–2019 session has ended.
2018–2019 Session
Senate Bill 2086
Establishes central registry for sickle cell trait diagnoses; provides for informational outreach and genetic counseling.
Sponsors
Who carried the bill in each chamber, and who signed on. Each name leads to the member's page.
In the Senate
Sponsor from Feb 26
Chief co-sponsor from Jun 7
Its course
March 5 to May 21, 2018, on one scale. In the top row each mark is a day something happened; taller marks are busier days.
Each committee stop sits inside its chamber.
Every action4 actions on 4 days
In the SenateMar 5 to May 21 · stopped77 days
Health, Human Services and Senior CitizensMar 5 to Mar 127 days
Budget and AppropriationsMar 13 to May 2169 days
Text
Each version as the Legislature printed it.
l9n doesn't hold this bill's text yet.
What happened
In l9n's words, one line for each step. Every action as the Legislature published it is below.
In the Senate Mar 5 – May 21
- Mar 5Introduced in the Senate and sent to Health, Human Services and Senior Citizens
- Mar 12Health, Human Services and Senior Citizens recommended it
- Read a second time
- Mar 13Sent to Budget and Appropriations
- May 21Budget and Appropriations recommended it
- Read a second time