What's happening
This resolution urges the Governor to designate September 10-16, 2017, as Duchenne Muscular Dystrophy Awareness Week in New York.
Why it matters
Raising public awareness about Duchenne Muscular Dystrophy (DMD) can help families and medical professionals recognize early signs, leading to earlier diagnosis and potentially better management of the disease.
Highlighting the lack of a cure and the need for accelerated research could increase funding and advocacy efforts, potentially speeding up the development of new treatments and support for those affected.
The resolution brings attention to both the genetic and spontaneous nature of DMD, emphasizing that it can affect any family, which may reduce stigma and encourage broader community support.
By formally recognizing organizations like Jar of Hope and the efforts of scientists, the resolution fosters collaboration between policymakers, advocacy groups, and researchers, potentially paving the way for more coordinated efforts in combating DMD.
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Headline styles
Duchenne Awareness Week Proclaimed
Plain English, a few words. Used as the page title.
Sponsors
59 Multi-sponsors
- Peter Abbate
- Thomas Abinanti
- William A. Barclay
- Didi Barrett
- Michael Blake
- Kenneth Blankenbush
- Edward Braunstein
- Vivian Cook
- Marcos Crespo
- Clifford Crouch
- Michael DenDekker
- Anthony D'Urso
- Steven Englebright
- Joseph Errigo
- Patricia Fahy
- Michael J. Fitzpatrick
- Sandy Galef
- Joseph Giglio
- Mark Gjonaj
- Deborah Glick
- Richard Gottfried
- Aileen Gunther
- Pamela Harris
- Stephen Hawley
- Earlene Hooper
- Alicia Hyndman
- Mark C. Johns
- Billy Jones
- Charles Lavine
- Donna Lupardo
- Chad A. Lupinacci
- John T. McDonald III
- David McDonough
- Thomas McKevitt
- Steven McLaughlin
- Michael G. Miller
- Melissa Miller
- Michael Montesano
- Angelo J. Morinello
- Walter T. Mosley
- Robert Oaks
- Felix Ortiz
- Philip Palmesano
- Crystal Peoples-Stokes
- N. Nick Perry
- Edward Ra
- Andrew Raia
- Linda Rosenthal
- Rebecca Seawright
- Aravella Simotas
- James Skoufis
- Dan Stec
- Fred Thiele
- Mary Beth Walsh
- Raymond Walter
- David Weprin
- Carrie Woerner
- Tremaine Wright
- Kenneth Zebrowski
History
- Adopted
- Referred to calendar
Full text
1 pageUnderlined is new[Struck] is removedOfficial text on nysenate.gov ↗
Assembly Resolution No. 602 BY: M. of A. Cusick MEMORIALIZING Governor Andrew M. Cuomo to proclaim September 10-16, 2017, as Duchenne Muscular Dystrophy Awareness Week in the State of New York WHEREAS, It is the custom of this Legislative Body to recognize… Show allHide
Assembly Resolution No. 602 BY: M. of A. Cusick MEMORIALIZING Governor Andrew M. Cuomo to proclaim September 10-16, 2017, as Duchenne Muscular Dystrophy Awareness Week in the State of New York WHEREAS, It is the custom of this Legislative Body to recognize official weeks that are set aside to increase awareness of serious illnesses that affect the lives of citizens of New York State; and WHEREAS, Attendant to such concern, and in full accord with its long-standing traditions, this Legislative Body is justly proud to memorialize Governor Andrew M. Cuomo to proclaim September 10-16, 2017, as Duchenne Muscular Dystrophy Awareness Week in the State of New York, in conjunction with the observance of National Duchenne Muscular Dystrophy Awareness Week; and WHEREAS, Duchenne muscular dystrophy is the most common fatal genetic disorder diagnosed in childhood, affecting approximately one in every 3,500 live male births (about 20,000 new cases each year worldwide); since the Duchenne gene is found on the X-chromosome, it primarily affects boys, however, it occurs across all races and cultures; and WHEREAS, Duchenne muscular dystrophy results in progressive loss of strength and is caused by a mutation in the gene that encodes for dystrophin; since dystrophin is absent, the muscle cells are easily damaged; and WHEREAS, The progressive muscle weakness leads to serious medical problems, particularly issues relating to the heart and lungs; young men with this debilitating disease typically live into their late twenties; and WHEREAS, Becker muscular dystrophy, which is less severe than Duchenne muscular dystrophy, occurs when dystrophin is manufactured, but not in the normal folin or amount; and WHEREAS, Duchenne muscular dystrophy can be passed from parent to child, but approximately 35% of cases occur because of a random spontaneous mutation; in other words, it can affect anyone; and WHEREAS, Although there are medical treatments that may help slow its progression, there is currently no cure for Duchenne muscular dystrophy; and WHEREAS, Jar of Hope's mission is to find a cure through accelerated research, calls for action in Washington D.C., demand optimal care for all young men, and educate the global community; and WHEREAS, Scientists around the globe are conducting intense research to understand what causes muscle dysfunction in Duchenne muscular dystrophy and to apply that understanding to the development of effective treatments; and WHEREAS, National Duchenne Muscular Dystrophy Awareness Week will highlight the importance of identifying and communicating early signs of this genetic disorder which is the key to early diagnosis; now, therefore, be it RESOLVED, That this Legislative Body pause in its deliberations to memorialize Governor Andrew M. Cuomo to proclaim September 10-16, 2017, as Duchenne Muscular Dystrophy Awareness Week in the State of New York; and be it further RESOLVED, That copies of this Resolution, suitably engrossed, be transmitted to The Honorable Andrew M. Cuomo, Governor of the State of New York; and Jar of Hope.
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