Overview
What is Sickle Cell Disease Foundation?
The Sickle Cell Disease Foundation, based in Ontario, California, is a dedicated nonprofit organization that works tirelessly to improve the lives of individuals affected by Sickle Cell Disease. Their primary mission is to establish a supportive environment where these individuals can receive comprehensive, patient-centered, coordinated, accessible, safe, and high-quality care, regardless of their location within California. They accomplish this by collaborating with healthcare providers, agencies, and the community through the Networking California for Sickle Cell Care (NCSCC) initiative. This collaborative effort aims to create a cohesive plan that sets specific goals to ensure optimal care for individuals with Sickle Cell Disease. The Sickle Cell Disease Foundation partners with the Center for Inherited Blood Disorders, a non-profit hematology center of excellence, to provide education, support, and multidisciplinary services to both children and adults with Sickle Cell Disease and other inherited disorders. The organization's ultimate goal is to build a world where individuals living with Sickle Cell Disease can expect the care and compassion they deserve. With a workforce of 29 dedicated individuals, the Sickle Cell Disease Foundation is committed to making a significant impact in the lives of those affected by this condition.
Official website here: www.scdfc.org
Is Sickle Cell Disease Foundation legitimate?
Sickle Cell Disease Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. Sickle Cell Disease Foundation 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: $293,206
Professional Fundraising Fees: $0
Other Salaries and Wages: $1,227,835
For more financial information, click here
Official website here: www.scdfc.org
What is the mission statement of Sickle Cell Disease Foundation?
The Sickle Cell Disease Foundation's mission is geared towards creating a world where individuals affected by Sickle Cell Disease receive the necessary care and compassion they deserve. They strive to achieve this by collaborating with providers, agencies, and the community to develop and implement a comprehensive, patient-centered, coordinated, accessible, safe, and high-quality care plan for individuals with Sickle Cell Disease, regardless of their location or healthcare provider. This mission is carried out in partnership with the Center for Inherited Blood Disorders, a non-profit organization providing education, support, and multidisciplinary services to adults and children with various inherited disorders.
Official website here: www.scdfc.org
Who is the CEO of Sickle Cell Disease Foundation?
Mary E Brown is the President & Ceo of Sickle Cell Disease Foundation. The CEO's salary of Sickle Cell Disease Foundation is $202,098 and their total compensation is $202,098.
Official website here: www.scdfc.org
What is the revenue of Sickle Cell Disease Foundation?
Sickle Cell Disease Foundation's revenue in 2022 was $2,848,547.
Official website here: www.scdfc.org
Who are the executives of Sickle Cell Disease Foundation and what are their salaries?
The average compensation at Sickle Cell Disease Foundation during 2022 was $52,450. There are 29 employees and 150 volunteers at Sickle Cell Disease Foundation.
Here are 19 key members and their salaries (Sickle Cell Disease Foundation's CEO's salary is $202,098 and their total compensation is $202,098):
- Compensation: $202,098
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- Other: $0
- Compensation: $101,017
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- Compensation: $91,108
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Official website here: www.scdfc.org
Where can I find the form 990 for Sickle Cell Disease Foundation?
Sickle Cell Disease Foundation's most recent form 990 was submitted in 2022 and can be accessed here.
Official website here: www.scdfc.org
Learn more at the official website: www.scdfc.org
Mission Statement of Sickle Cell Disease Foundation
The Sickle Cell Disease Foundation aims to establish a world where individuals afflicted with Sickle Cell Disease receive the necessary care and compassion. To achieve this goal, the foundation collaborates with various providers, agencies, and the community to develop and implement a cohesive plan. This plan is designed to ensure that people with Sickle Cell Disease receive comprehensive, patient-centered, coordinated, accessible, safe, and high-quality care, regardless of their location or chosen healthcare provider in California. The Sickle Cell Disease Foundation partners with the Center for Inherited Blood Disorders, a non-profit hematology center of excellence, to provide education, support, and multidisciplinary, family-centered services to both adults and children living with various inherited disorders, including Sickle Cell Disease.
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Impact
October, 2024
The Sickle Cell Disease Foundation significantly impacts the lives of individuals living with Sickle Cell Disease by fostering a collaborative healthcare approach through the Networking California for Sickle Cell Care (NCSCC) initiative. This effort ensures that patients receive comprehensive, patient-centered, and high-quality care, no matter where they are in California. By bringing together healthcare providers, agencies, and community members, the foundation works to implement a cohesive plan that establishes specific goals for accessible and safe healthcare services.
Through its partnership with the Center for Inherited Blood Disorders, the foundation enhances the supports available, offering education and multidisciplinary services to both adults and children affected by inherited blood disorders. The foundation’s commitment to building a compassionate care environment encourages improved health outcomes and quality of life for those living with Sickle Cell Disease, ultimately creating a more informed and supportive community.
This information is meant to be a general summary of Sickle Cell Disease Foundation. 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.
- Program Service Revenue: $2,017,417
- Gross Receipts: $2,848,547
Assets and Liabilities:
- Total Assets: $4,364,809
- Total Liabilities: $1,528,117
- Net Assets: $2,836,692
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Programs
Programs are reported by nonprofits in their tax forms and are normally their tax-exempt activities.
Contracts
Revenue
$339,975
Subawards
Revenue
$1,677,442
Organization Details
Founding Year
1957
Phone
(909) 743-5226Principal Officer
Mary E Brown
Main Address
3602 Inland Empire Blvd Suite C315, Ontario, CA, 91764
Website
www.scdfc.orgNTEE Category
Code: G30 - Disease
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