Assembly Actions -
Lowercase Senate Actions - UPPERCASE |
|
---|---|
Oct 23, 2013 |
signed chap.428 |
Oct 11, 2013 |
delivered to governor |
Jun 18, 2013 |
returned to assembly passed senate 3rd reading cal.1425 substituted for s2186a |
Jun 10, 2013 |
referred to finance delivered to senate passed assembly ordered to third reading rules cal.70 rules report cal.70 reported |
Jun 03, 2013 |
reported referred to rules |
May 13, 2013 |
print number 962a |
May 13, 2013 |
amend (t) and recommit to ways and means |
Apr 16, 2013 |
reported referred to ways and means |
Jan 09, 2013 |
referred to health |
Assembly Bill A962A
Signed By Governor2013-2014 Legislative Session
Sponsored By
KELLNER
Archive: Last Bill Status - Signed by Governor
- Introduced
-
- In Committee Assembly
- In Committee Senate
-
- On Floor Calendar Assembly
- On Floor Calendar Senate
-
- Passed Assembly
- Passed Senate
- Delivered to Governor
- Signed By Governor
Actions
Votes
Bill Amendments
co-Sponsors
Clifford Crouch
Gary Finch
Richard Gottfried
multi-Sponsors
Brian F. Curran
Michael Cusick
Andrew Hevesi
Joseph Lentol
2013-A962 - Details
2013-A962 - Bill Text download pdf
S T A T E O F N E W Y O R K ________________________________________________________________________ 962 2013-2014 Regular Sessions I N A S S E M B L Y (PREFILED) January 9, 2013 ___________ Introduced by M. of A. KELLNER, CROUCH, FINCH -- Multi-Sponsored by -- M. of A. CURRAN, CUSICK, HEVESI, LUPARDO, MARKEY, WALTER -- read once and referred to the Committee on Health AN ACT to amend the public health law and the social services law, in relation to providing that persons with hemophilia and other clotting protein deficiencies who are otherwise eligible for the Child Health Plus or Family Health Plus programs shall have access to reimbursement for outpatient blood clotting factor concentrates and other necessary treatments and services THE PEOPLE OF THE STATE OF NEW YORK, REPRESENTED IN SENATE AND ASSEM- BLY, DO ENACT AS FOLLOWS: Section 1. Legislative findings. Hemophilia is a rare hereditary bleeding disorder resulting from a deficiency in blood proteins known as clotting factors. Without an adequate supply of clotting factors, indi- viduals can experience prolonged bleeding following routine medical and dental procedures, trauma, and a range of physical activities. Addi- tionally, individuals with hemophilia often experience spontaneous internal bleeding that can cause severe joint damage, chronic pain, and even death. Prior to the 1970s, individuals with hemophilia seldom lived beyond the age of 30 years. Early treatment consisted of whole blood and plasma transfusions at hospitals. These treatments were difficult, time consum- ing and only minimally effective. The advent of commercially prepared blood clotting factors in the 1980s represented a major advance in treatment, both in terms of efficacy and convenience. Most importantly, these advances allowed for home infusion. In addition to hemophilia, there are several other disorders resulting from blood protein deficiencies. These include Von Willebrand Disease (VWD), the most common bleeding disorder, affecting approximately two million Americans. Individuals with the severest form of VWD rely on EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets [ ] is old law to be omitted.
co-Sponsors
Clifford Crouch
Gary Finch
Richard Gottfried
Joseph Morelle
multi-Sponsors
Brian F. Curran
Michael Cusick
Andrew Hevesi
Joseph Lentol
2013-A962A (ACTIVE) - Details
2013-A962A (ACTIVE) - Bill Text download pdf
S T A T E O F N E W Y O R K ________________________________________________________________________ 962--A 2013-2014 Regular Sessions I N A S S E M B L Y (PREFILED) January 9, 2013 ___________ Introduced by M. of A. KELLNER, CROUCH, FINCH, GOTTFRIED -- Multi-Spon- sored by -- M. of A. CURRAN, CUSICK, HEVESI, LENTOL, LUPARDO, MARKEY, MOSLEY, WALTER -- read once and referred to the Committee on Health -- reported and referred to the Committee on Ways and Means -- committee discharged, bill amended, ordered reprinted as amended and recommitted to said committee AN ACT to amend the public health law, in relation to providing that persons with hemophilia and other clotting protein deficiencies who are otherwise eligible for the Child Health Plus program shall have access to reimbursement for outpatient blood clotting factor concen- trates and other necessary treatments and services THE PEOPLE OF THE STATE OF NEW YORK, REPRESENTED IN SENATE AND ASSEM- BLY, DO ENACT AS FOLLOWS: Section 1. Legislative findings. Hemophilia is a rare hereditary bleeding disorder resulting from a deficiency in blood proteins known as clotting factors. Without an adequate supply of clotting factors, indi- viduals can experience prolonged bleeding following routine medical and dental procedures, trauma, and a range of physical activities. Addi- tionally, individuals with hemophilia often experience spontaneous internal bleeding that can cause severe joint damage, chronic pain, and even death. Prior to the 1970s, individuals with hemophilia seldom lived beyond the age of 30 years. Early treatment consisted of whole blood and plasma transfusions at hospitals. These treatments were difficult, time consum- ing and only minimally effective. The advent of commercially prepared blood clotting factors in the 1980s represented a major advance in treatment, both in terms of efficacy and convenience. Most importantly, these advances allowed for home infusion. In addition to hemophilia, there are several other disorders resulting from blood protein deficiencies. These include Von Willebrand Disease EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets [ ] is old law to be omitted.
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