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 18, 2013 |
substituted by a962a ordered to third reading cal.1425 committee discharged and committed to rules |
Jun 10, 2013 |
reported and committed to finance |
May 22, 2013 |
print number 2186a |
May 22, 2013 |
amend (t) and recommit to health |
Jan 14, 2013 |
referred to health |
Senate Bill S2186A
Signed By Governor2013-2014 Legislative Session
Sponsored By
(R, C, IP) Senate District
Archive: Last Bill Status Via A962 - 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
(D, WF) Senate District
(D, WF) 46th Senate District
(R, IP) Senate District
(R, C, IP) Senate District
2013-S2186 - Details
2013-S2186 - Sponsor Memo
BILL NUMBER:S2186 TITLE OF BILL: 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 PURPOSE: To provide outpatient coverage under the Child Health Plus, Family Health Plus, and Healthy New York programs for blood clotting factor concentrates as well as other treatments and services necessary for individuals with hemophilia and other clotting protein deficiencies. SUMMARY OF PROVISIONS: Subdivision 7 of section 2510 of the public health law, as amended by section 21 of part B of chapter 109 of the laws of 2010, is amended to include: *outpatient blood clotting factor products and other treatments and services furnished in connection with the care of hemophilia and other blood clotting protein deficiencies; Paragraph a of subdivision 7 of section 2510 of the public health law, as amended by chapter 526 of the laws of 2002 is amended to include: * outpatient blood clotting factor products and other treatments and
2013-S2186 - Bill Text download pdf
S T A T E O F N E W Y O R K ________________________________________________________________________ 2186 2013-2014 Regular Sessions I N S E N A T E January 14, 2013 ___________ Introduced by Sen. ROBACH -- read twice and ordered printed, and when printed to be committed 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 clotting factor treatments similar to those used by individuals with hemophilia. EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets [ ] is old law to be omitted. LBD02168-01-3
co-Sponsors
(D, WF) 46th Senate District
(R, IP) Senate District
(R, C) Senate District
(R, C, IP) Senate District
2013-S2186A (ACTIVE) - Details
2013-S2186A (ACTIVE) - Sponsor Memo
BILL NUMBER:S2186A TITLE OF BILL: 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 concentrates and other necessary treatments and services PURPOSE: To provide outpatient coverage under the Child Health Plus, Family Health Plus, and Healthy New York programs for blood clotting factor concentrates as well as other treatments and services necessary for individuals with hemophilia and other clotting protein deficiencies. SUMMARY OF PROVISIONS: Subdivision 7 of section 2510 of the public health law, as amended by section 21 of part B of chapter 109 of the laws of 2010, is amended to include: *outpatient blood clotting factor products and other treatments and services furnished in connection with the care of hemophilia and other blood clotting protein deficiencies; Paragraph a of subdivision 7 of section 2510 of the public health law, as amended by chapter 526 of the laws of 2002 is amended to include:
2013-S2186A (ACTIVE) - Bill Text download pdf
S T A T E O F N E W Y O R K ________________________________________________________________________ 2186--A 2013-2014 Regular Sessions I N S E N A T E January 14, 2013 ___________ Introduced by Sens. ROBACH, ADAMS, BRESLIN, GRISANTI, MARCHIONE, NOZZO- LIO, PARKER, VALESKY -- read twice and ordered printed, and when printed to be committed to the Committee on Health -- 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 (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. LBD02168-05-3
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