As Passed by the Senate

130th General Assembly
Regular Session
2013-2014
Am. H. B. No. 105


Representative Hayes 

Cosponsors: Representatives Derickson, Beck, Milkovich, Strahorn, Wachtmann, Antonio, Bishoff, Brown, Hottinger, Adams, R., Amstutz, Anielski, Ashford, Baker, Blair, Boose, Buchy, Budish, Burkley, Carney, Green, Grossman, Hackett, Hagan, C., Hall, Landis, McClain, O'Brien, Patmon, Pelanda, Ramos, Reece, Roegner, Rogers, Sears, Slaby, Smith, Sprague, Stebelton, Young Speaker Batchelder 

Senators Tavares, Brown, Burke, Coley, Eklund, Hite, Hughes, Jones, Kearney, Lehner, Manning, Obhof, Oelslager, Patton, Peterson, Schaffer, Turner, Uecker, Widener 



A BILL
To enact section 5.2280 of the Revised Code to 1
designate the calendar week including the 2
seventeenth day of July as "Congenital 3
Diaphragmatic Hernia Week."4


BE IT ENACTED BY THE GENERAL ASSEMBLY OF THE STATE OF OHIO:

       Section 1.  That section 5.2280 of the Revised Code be 5
enacted to read as follows:6

       Sec. 5.2280.  The calendar week including the seventeenth day 7
of July is designated as "Congenital Diaphragmatic Hernia Week." 8

       Section 2.  In enacting section 5.2280 of the Revised Code, 9
it is the intent of the General Assembly to increase public 10
awareness and understanding of congenital diaphragmatic hernias. 11
The General Assembly considers it vitally important that the state 12
designate the calendar week including the seventeenth of July as 13
"Congenital Diaphragmatic Hernia Week." According to CHERUBS - The 14
Association of Congenital Diaphragmatic Hernia Research, Awareness 15
and Support, a congenital diaphragmatic hernia (CDH) occurs when 16
the diaphragm fails to form fully, which allows the abdominal 17
organs to move into the chest cavity and prevents lung growth. CDH 18
occurs in 1,600 babies every year in the United States. The state 19
encourages and commends private efforts, including those of 20
CHERUBS, to enhance funding for CDH research, provide educational 21
materials and programs, and create a support network for families 22
affected by this devastating birth defect.23