Overview
What is National Alliance Of Sickle Cell Centers?
The National Alliance of Sickle Cell Centers is a nonprofit organization situated in Washington, D.C., specifically at 1129 20th street NW suite 400. Their primary mission involves supporting sickle cell disease centers in offering superior quality, all-encompassing care. They achieve this by establishing standards, advocating for their adoption, identifying resources, and strengthening these centers. The organization has received funding from various sources, including industry companies and grants, to initiate research and assess outcomes from new medications and treatments for sickle cell disease. Currently, their funds are utilized with the exception of operating expenses.
Official website here: www.sicklecellcenters.org
Is National Alliance Of Sickle Cell Centers legitimate?
National Alliance Of Sickle Cell Centers is a legitimate nonprofit organization registered as a 501(c)(3) entity. National Alliance Of Sickle Cell Centers 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: $0
For more financial information, click here
Official website here: www.sicklecellcenters.org
What is the mission statement of National Alliance Of Sickle Cell Centers?
The National Alliance of Sickle Cell Centers' mission is centered around supporting sickle cell disease centers in providing top-notch, comprehensive care. They achieve this by establishing standards, promoting their implementation, identifying opportunities and resources to enhance these centers, and advocating for access to comprehensive care. This mission aims to improve health outcomes, enhance the quality of life, and boost survival rates for individuals with sickle cell disease. The alliance also strives to strengthen these centers, enabling them to deliver optimal care.
Official website here: www.sicklecellcenters.org
Who is the CEO of National Alliance Of Sickle Cell Centers?
Julie Kanter Washko is the Consultant of National Alliance Of Sickle Cell Centers.
Official website here: www.sicklecellcenters.org
What is the revenue of National Alliance Of Sickle Cell Centers?
National Alliance Of Sickle Cell Centers's revenue in 2022 was $400,100.
Official website here: www.sicklecellcenters.org
Who are the executives of National Alliance Of Sickle Cell Centers and what are their salaries?
There 11 volunteers at National Alliance Of Sickle Cell Centers.
Here are 8 key members and their salaries:
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- Compensation: $2,925
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- Compensation: $21,380
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- Compensation: $6,500
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- Compensation: $2,400
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Official website here: www.sicklecellcenters.org
Where can I find the form 990 for National Alliance Of Sickle Cell Centers?
National Alliance Of Sickle Cell Centers's most recent form 990 was submitted in 2022 and can be accessed here.
Official website here: www.sicklecellcenters.org
Learn more at the official website: www.sicklecellcenters.org
Mission Statement of National Alliance Of Sickle Cell Centers
The National Alliance of Sickle Cell Centers, as an organization, is committed to supporting sickle cell disease centers in delivering top-notch, comprehensive care. Their mission involves setting standards, advocating for their adoption, and identifying opportunities and resources to enhance the centers' capabilities. This aim is to improve health outcomes, enhance the quality of life, and increase survival rates for individuals living with sickle cell disease. The alliance also works towards advocating for broader access to comprehensive care, with the ultimate goal of enhancing the overall well-being of those affected by the condition. The organization has successfully secured funding from various sources, including industry companies and grants, to initiate research and assess the effectiveness of new medications and therapies for people with sickle cell disease.
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Impact
October, 2024
The National Alliance of Sickle Cell Centers plays a critical role in enhancing the quality of care for individuals living with sickle cell disease (SCD). By supporting specialized SCD centers, the organization sets standards and promotes their adoption, ensuring that patients receive comprehensive and high-quality treatment. Through its initiatives, it identifies opportunities and resources aimed at strengthening these care centers, fostering a collaborative approach to improving health outcomes.
Moreover, the Alliance advocates for access to comprehensive care, which is vital for enhancing the quality of life and survival rates of those affected by SCD. Recent efforts, including securing funding for startup projects and conducting retrospective studies to evaluate the effectiveness of new medications and therapies, reflect its commitment to advancing treatment options and understanding patient outcomes. By focusing on both advocacy and resource development, the National Alliance of Sickle Cell Centers significantly impacts the health landscape for individuals with sickle cell disease.
This information is meant to be a general summary of National Alliance Of Sickle Cell Centers. 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: $1,129
- Gross Receipts: $400,100
Assets and Liabilities:
- Total Assets: $489,851
- Total Liabilities: $0
- Net Assets: $489,851
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Organization Details
Founding Year
2020
Phone
(205) 761-3785Principal Officer
Julie Kanter Washko
Main Address
1129 20th street NW suite 400, Washington, DC, 20036
Website
www.sicklecellcenters.orgNTEE Category
Code: G20 - Disease
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