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NYS Sickle Cell Advocacy Network Inc

Queens Village, NY · EIN 113373180 · Form 990EZ · FY2019 · Micro (<$100K)
revenue
$32K
expenses
$44K
net assets
$0
employees
mission · from form 990

Education and support

profile · synthesized from sources

NYS Sickle Cell Advocacy Network Inc is a nonprofit organization based in New York that provides education and support services related to sickle cell disease. The organization focuses on raising awareness, offering patient and family support, and promoting public understanding of the condition. Its activities are centered on community outreach and health advocacy within New York State.

named programs · 2 · from sources

What they call their work

Patient and Family Support Services
Offers counseling, resource navigation, and peer support for individuals and families affected by sickle cell disease
Sickle Cell Education Outreach
Provides community-based educational programs about sickle cell disease, including screening, inheritance, and management
activities · 1 group

What they do

  • Bleeding and Blood Disorder Support Services 1 activity
    • Provide education and support services
      Offers educational resources and support services related to sickle cell disease, including patient and community outreach programs.
financials · form 990EZ · fy2019
revenue
Total revenue$32K
Contributions & grants$32K100%
Program service revenue
Investment income
Other revenue
expenses
Total expenses$44K
Program expenses
Admin / overhead
Fundraising
Salaries & benefits
Grants paid out
balance sheet
Total assets$15K
Cash
Investments
Liabilities
Net assets$0
2 years on record · 2018–2019 · YoY revenue -32.0%
leadership · form 990 part vii · fy2019

Who runs it

board members · 1
  • GLORIA ROCESTER — Director
strategies · 1

How they approach the work

Named approaches extracted from this org’s sources. Where others share an approach, follow it to see the full set of orgs running it.

  • Education and Support for Sickle Cell Disease
    methodology: education_and_support
    By providing education and support services, the organization aims to improve health outcomes and quality of life for individuals affected by sickle cell disease, because informed patients and caregivers can better manage the condition and navigate healthcare systems.