Overview
What is Sickle Cell Thalassemia Patients Networks Inc?
Sickle Cell Thalassemia Patients Networks Inc, abbreviated as SCTPN, is a dedicated nonprofit organization based in Brooklyn, New York. Their mission revolves around enhancing the lives of individuals and families affected by Sickle Cell Disease, Thalassemia, and other hemoglobin disorders. They aim to improve quality of life through various initiatives such as education, advocacy, and support interactions. SCTPN actively promotes academic excellence in children and young adults living with these conditions by offering tutorial services, achievement awards, and college scholarships. The organization's headquarters can be found at 1139 St. Johns Place, Brooklyn, NY 11213, and it employs a team of 12 individuals dedicated to their cause.
Official website here: www.sctpn.net
Is Sickle Cell Thalassemia Patients Networks Inc legitimate?
Sickle Cell Thalassemia Patients Networks Inc is a legitimate nonprofit organization registered as a 501(c)(3) entity. Sickle Cell Thalassemia Patients Networks Inc submitted a form 990, which is a tax form used by tax-exempt organizations in the U.S., indicating its operational transparency and adherence to regulatory requirements. Donations to this organization are tax deductible.
Heare are some key statistics you may want to consider:
Executive Compensation: $0
Professional Fundraising Fees: $0
Other Salaries and Wages: $99,654
For more financial information, click here
Official website here: www.sctpn.net
What is the mission statement of Sickle Cell Thalassemia Patients Networks Inc?
The Sickle Cell Thalassemia Patients Networks Inc is committed to enhancing the quality of life for individuals and families affected by Sickle Cell Disease, Thalassemia, and other hemoglobin disorders. They accomplish this through three main avenues: education, advocacy, and support. The educational aspect involves promoting academic excellence in children and young adults living with these conditions through tutorial services, achievement awards, and college scholarships. In addition to education, they also provide referrals to resources that can help mitigate the negative emotional, psychological, social, and economic impact of these debilitating conditions. The organization's mission is to interact with individuals and families, offering them the necessary support to navigate their daily lives more effectively.
Official website here: www.sctpn.net
Who is the CEO of Sickle Cell Thalassemia Patients Networks Inc?
Teresa Ginger Davis is the President of Sickle Cell Thalassemia Patients Networks Inc.
Official website here: www.sctpn.net
What is the revenue of Sickle Cell Thalassemia Patients Networks Inc?
Sickle Cell Thalassemia Patients Networks Inc's revenue in 2022 was $301,033.
Official website here: www.sctpn.net
Who are the executives of Sickle Cell Thalassemia Patients Networks Inc and what are their salaries?
The average compensation at Sickle Cell Thalassemia Patients Networks Inc during 2022 was $8,304. There are 12 employees and 25 volunteers at Sickle Cell Thalassemia Patients Networks Inc.
Here are 5 key members and their salaries:
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- Compensation: $23,075
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Official website here: www.sctpn.net
Where can I find the form 990 for Sickle Cell Thalassemia Patients Networks Inc?
Sickle Cell Thalassemia Patients Networks Inc's most recent form 990 was submitted in 2022 and can be accessed here.
Official website here: www.sctpn.net
Learn more at the official website: www.sctpn.net
Mission Statement of Sickle Cell Thalassemia Patients Networks Inc
Sickle Cell Thalassemia Patients Networks Inc, a nonprofit organization, is committed to enhancing the quality of life for individuals and families affected by Sickle Cell Disease, Thalassemia, and other hemoglobin disorders. Their mission is threefold: education, advocacy, and support. They strive to promote academic excellence in children and young adults living with these conditions through tutorial services, achievement awards, and college scholarships. This educational component aims to equip these individuals with the necessary skills and knowledge to overcome the challenges posed by their conditions.
Beyond education, Sickle Cell Thalassemia Patients Networks Inc also engages in advocacy efforts. They aim to diminish the negative emotional, psychological, social, and economic impact of these debilitative conditions by advocating for resources and support. Their advocacy work seeks to create a more inclusive and supportive environment for individuals living with these conditions.
Lastly, Sickle Cell Thalassemia Patients Networks Inc provides referrals to resources that can help mitigate the impact of these conditions. They offer support interaction, connecting individuals and families with the resources they need to navigate their daily lives more effectively. This holistic approach to care ensures that individuals and families living with Sickle Cell Disease, Thalassemia, and other hemoglobin disorders have the resources and support they need to live fulfilling lives.
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Impact
October, 2024
Sickle Cell Thalassemia Patients Networks Inc significantly enhances the quality of life for individuals and families affected by Sickle Cell Disease, Thalassemia, and other hemoglobin disorders. By promoting academic excellence among children and young adults, they offer tutorial services, achievement awards, and college scholarships, empowering the next generation to pursue their educational goals despite the challenges posed by these conditions.
Their annual benefit awards not only recognize the essential contributions of caregivers but also foster a sense of community and support within the Sickle Cell community. Through education, advocacy, and comprehensive support interactions, SCTPN addresses the emotional, psychological, social, and economic challenges faced by patients and their families. Furthermore, they provide valuable referrals to resources that help alleviate the burdens associated with these debilitating diseases, ensuring that individuals receive the support they need to thrive.
Overall, SCTPN plays a pivotal role in creating a nurturing environment that encourages resilience and academic success while fostering a strong community connection for those impacted by these conditions.
This information is meant to be a general summary of Sickle Cell Thalassemia Patients Networks Inc. Please take the time to review official sources before making any decisions based upon the content provided here.
Financials
This financial information is from Propublica.
Other financial information:
This information is from the most recently submitted tax form from this organization, which was in 2022.
- Investment Income: $5
- Gross Receipts: $301,033
Assets and Liabilities:
- Total Assets: $127,418
- Total Liabilities: $22,219
- Net Assets: $105,199
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Organization Details
Founding Year
1992
Phone
(347) 533-8485Principal Officer
Teresa Ginger Davis
Main Address
1139 ST JOHNS PLACE, Brooklyn, NY, 11213
Website
www.sctpn.netNTEE Category
Code: G20 - Disease
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