Overview
What is Supporters Of Families With Sickle Cell Disease?
Supporters of Families with Sickle Cell Disease is a nonprofit organization situated in Tulsa, Oklahoma, with the US address 5424 N Madison Ave 74126. Their primary mission is to enhance knowledge, awareness, advocacy, and support for individuals living with chronic health conditions, particularly Sickle Cell Disease, in underserved communities within Oklahoma. They achieve this goal through various outreach programs, reaching over 4,500 participants annually. Their activities aim to improve the quality of life for patients and their families by promoting self-efficacy, advocating for systemic changes in patient care, disability policies, education, and family support. They also strive for economic self-sufficiency and increased awareness of the disease. Their objective is to expand their reach by 10% in the coming years.
Official website here: www.sicklecelloklahoma.org
Is Supporters Of Families With Sickle Cell Disease legitimate?
Supporters Of Families With Sickle Cell Disease is a legitimate nonprofit organization registered as a 501(c)(3) entity. Supporters Of Families With Sickle Cell Disease 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.
Here are some key statistics you may want to consider:
Executive Compensation: $0
Professional Fundraising Fees: $0
Other Salaries and Wages: $0
For more financial information, click here
Official website here: www.sicklecelloklahoma.org
What is the mission statement of Supporters Of Families With Sickle Cell Disease?
Supporters of Families with Sickle Cell Disease aims to enhance the self-confidence and improve the overall well-being of individuals and their families suffering from Sickle Cell and Thalassemia. This is achieved by implementing systemic changes in healthcare, disability policies, education, family support, economic self-sufficiency, awareness, and advocacy. Their mission is carried out through various outreach programs annually, reaching over four thousand five hundred participants, with an aim to expand their reach by 10% in the near future. The organization works towards increasing awareness and support for individuals living with chronic health conditions in underserved communities.
Official website here: www.sicklecelloklahoma.org
Who is the CEO of Supporters Of Families With Sickle Cell Disease?
Velvet Brown is the Executive Director of Supporters Of Families With Sickle Cell Disease.
Official website here: www.sicklecelloklahoma.org
What is the revenue of Supporters Of Families With Sickle Cell Disease?
Supporters Of Families With Sickle Cell Disease's revenue in 2022 was $663,494.
Official website here: www.sicklecelloklahoma.org
Who are the executives of Supporters Of Families With Sickle Cell Disease and what are their salaries?
- Velvet Brown (Executive Director)
- Jeremiah Watts (Mhr*Cdd*Pastor)
- Cynthia Brooks (Secretary) [Trustee/Director]
- Lorice Cooper (Tresurer) [Trustee/Director]
- Jennittee Marshall (Chaplin) [Trustee/Director]
- Sherence Thompson (Scd Parent) [Trustee/Director]
- Shaquanda Lewis (Council Amb)
- Drew Diamond (Council Amb)
- Bonnie Johnson (Council Amb)
- Dr Marshan Oliver Marick (Council Amb)
- James Mchenry (Council Amb)
- Clifton Talbert (Council Amb)
- Barbara Talbert (Council Amb)
- Corrina Jackson (Council Amb)
- Ester Wilcox (Council Amb)
Official website here: www.sicklecelloklahoma.org
Where can I find the form 990 for Supporters Of Families With Sickle Cell Disease?
The Supporters Of Families With Sickle Cell Disease’s most recent form 990 was submitted in 2022 and can be accessed here
Official website here: www.sicklecelloklahoma.org
Learn more at the official website: www.sicklecelloklahoma.org
Mission Statement of Supporters Of Families With Sickle Cell Disease
Supporters of Families with Sickle Cell Disease is an organization dedicated to enhancing the self-efficacy and improving the overall quality of life for individuals and families affected by Sickle Cell and Thalassemia within Oklahoma. Their mission is multi-faceted, aiming to instigate systemic changes in patient care, disability policies, education, family support, economic self-sufficiency, awareness, and advocacy. By implementing these changes, the organization strives to significantly improve the lives of those living with these chronic health conditions.
In concrete terms, Supporters of Families with Sickle Cell Disease aims to increase awareness and knowledge about these conditions through various outreach programs. The organization has successfully reached over four thousand five hundred participants with this information annually, and they aim to expand their reach by 10% in the coming years. They believe that through strong community engagement and education, individuals and families can better navigate their health challenges and improve their overall well-being.
The organization's mission is not limited to awareness and education, however. They also advocate for systemic changes in patient care and disability policies. By working towards these goals, they aim to empower patients and their families to live more fulfilling lives, with improved access to essential resources and support. Supporters of Families with Sickle Cell Disease is committed to making a meaningful difference in the lives of those affected by these conditions, striving for a future where individuals and families can live with confidence and dignity.
Impact
This information is meant to be a general summary of Supporters Of Families With Sickle Cell Disease. Please take the time to review official sources before making any decisions based upon the content provided here.
Wednesday, July 24, 2024
Supporters Of Families With Sickle Cell Disease is making a significant impact by increasing self-efficacy and improving the overall quality of life for patients and their families living with Sickle Cell and Thalassemia in Oklahoma. Through systemic changes in patient care, disability policies, education, family support, economic self-sufficiency, awareness, and advocacy, they are providing crucial support to an underserved community. By conducting outreach programs and activities, they have reached out to thousands of participants, spreading knowledge and awareness about these chronic health conditions. Their goal of expanding their reach by 10% in the coming years shows their commitment to making a real difference in the lives of those affected by Sickle Cell Disease in Oklahoma.
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.
- Assets and Liabilities:
Programs
Programs are reported by nonprofits in their tax forms and are normally their tax-exempt activities.
GOVERNMENT PROGRAMS
Revenue
$569,146
Organization Details
Founding Year
2004
Phone
(918) 619-6174
Principal Officer
Velvet Brown
Main Address
5424 N Madison Ave, Tulsa, OK, 74126
Website
www.sicklecelloklahoma.org
NTEE Category
Code: E60 - Health
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