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K00498 Summary:

BILL NOK00498
 
SAME ASNo Same As
 
SPONSORShimsky
 
COSPNSR
 
MLTSPNSRSantabarbara
 
 
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K00498 Text:

 
Assembly Resolution No. 498
 
BY: M. of A. Shimsky
 
        MEMORIALIZING  Governor  Kathy  Hochul to proclaim
        May 2025 as Williams Syndrome Awareness Month in the
        State of New York
 
  WHEREAS, It is the custom of  this  Legislative  Body  to  recognize
official  months  which  are  set aside to increase awareness of serious
health issues that affect the lives of citizens  of  the  State  of  New
York; and
 
  WHEREAS,  It  is  the  sense of this Legislative Body to memorialize
Governor  Kathy  Hochul  to  proclaim  May  2025  as  Williams  Syndrome
Awareness Month in the State of New York; and
 
  WHEREAS,  Williams  Syndrome  (WS) is a genetic condition present at
birth and can affect anyone; it  is  characterized  by  various  medical
issues,  including  cardiovascular  disease,  developmental  delays, and
learning disabilities; these  medical  conditions  often  coincide  with
striking  verbal abilities, highly social personalities, and an affinity
for music; and
 
  WHEREAS, It is estimated that Williams Syndrome impacts one in every
10,000 individuals worldwide, including as many  as  30,000  within  the
United  States;  it  is known to occur equally in both males and females
and in every culture; and
 
  WHEREAS, As children with Williams Syndrome grow, many struggle with
issues like spatial relations, numbers, and abstract reasoning which can
render performing daily tasks a challenge; and
 
  WHEREAS, In adulthood, individuals with Williams Syndrome will often
need  supportive  housing  and  other  resources  to  reach  their  full
potential;  with  these  supports,  they can contribute greatly to their
communities as volunteers or paid employees in numerous fields; and
 
  WHEREAS, Camille Fortunato, as a parent of  a  child  with  Williams
Syndrome,  began  a  quest  for  appropriate educational and therapeutic
services for her son, Anthony; and
 
  WHEREAS, Camille Fortunato's son, Anthony, was very ill when he  was
born, and doctors were initially unable to determine what the underlying
issue  was; she and her husband, Stefano Filippazzo, took Anthony to see
cardiologists, pulmonologists, and critical  care  physicians;  it  took
years  of  excruciating searching to finally find the diagnosis for this
rare disease; and
 
  WHEREAS, Upon receiving Anthony's diagnosis, Camille  Fortunato  and
Stefano   Filippazzo  embarked  upon  a  commendable  pursuit  to  raise
awareness and capital for the Williams Syndrome  Association;  over  the
years,   they   have  participated  in  a  variety  of  very  successful
fundraising events; and
 
  WHEREAS, Founded in 1982, the Williams  Syndrome  Association  (WSA)
provides support to individuals with Williams Syndrome, as well as their
 
families,  connecting  them with professionals and other individuals who
can assist them in coping with the condition; and
 
  WHEREAS,  Through  this  organization's  efforts  of  raising public
awareness,  funding  critical  new  research,  and  providing   valuable
information  and  support to families, the Williams Syndrome Association
has improved the quality of  life  and  futures  of  those  affected  by
Williams Syndrome; and
 
  WHEREAS,  The Williams Syndrome Association, along with the families
and friends of  those  afflicted  with  Williams  Syndrome,  are  to  be
commended  for  their hard work, compassion, and dedication to educating
the citizens of the State of New York about  this  rare  disorder;  now,
therefore, be it
 
  RESOLVED,  That  this Legislative Body pause in its deliberations to
memorialize Governor Kathy Hochul  to  proclaim  May  2025  as  Williams
Syndrome Awareness Month in the State of New York; and be it further
 
  RESOLVED,  That  a  copy  of this Resolution, suitably engrossed, be
transmitted to The Honorable Kathy Hochul, Governor of the State of  New
York.
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