l9n/ New Jersey

2018–2019 Session

Assembly Bill 2184

Establishes central registry for sickle cell trait diagnoses; provides for informational outreach and genetic counseling.

Did not become law. It stopped in the Senate on May 21, 2018. The 2018–2019 session has ended.

Sponsors

Who carried the bill in each chamber, and who signed on. Each name leads to the member's page.

In the General Assembly

2 co-sponsors

Carol A. Murphy, Reed Gusciora

Its course

January 29 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 action9 actions on 8 days

In the General AssemblyJan 29 to Feb 1517 days

Health and Senior ServicesJan 29 to Jan 290 days

AppropriationsJan 29 to Feb 8 · moved on10 days

BudgetFeb 8 to Feb 124 days

In the SenateFeb 15 to May 21 · stopped95 days

Budget and AppropriationsMar 13 to May 2169 days

Votes

Yeas to nays, as the Legislature recorded them. Committee votes are set in.

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 General Assembly Jan 29 – Feb 15

  1. Introduced in the General Assembly and sent to Health and Senior Services
  2. Health and Senior Services recommended it
  3. Sent to Appropriations
  4. Sent to Budget
  5. Budget recommended it
  6. Read a second time
  7. Passed the General Assembly, 63 to 4

In the Senate Feb 22 – May 21

  1. Arrived in the Senate
  2. Sent to Health, Human Services and Senior Citizens
  3. Health, Human Services and Senior Citizens recommended it
  4. Read a second time
  5. Sent to Budget and Appropriations
  6. Budget and Appropriations recommended it
  7. Read a second time
All 9 actions, as published