Overview
What is Proteus Syndrome Foundation?
The Proteus Syndrome Foundation is a nonprofit organization committed to offering support to families affected by Proteus Syndrome. They achieve this through educational resources and connecting affected individuals with other families and medical experts. Additionally, they aim to raise funds for extensive professional health education, with the ultimate objective of identifying the root cause, developing treatments, and ultimately finding a cure for Proteus Syndrome.
Official website here: www.proteus-syndrome.org
Is Proteus Syndrome Foundation legitimate?
Proteus Syndrome Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. Proteus Syndrome 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: $20,000
Professional Fundraising Fees: $0
Other Salaries and Wages: $0
For more financial information, click here
Official website here: www.proteus-syndrome.org
What is the mission statement of Proteus Syndrome Foundation?
The Proteus Syndrome Foundation is committed to offering support to families affected by the condition, primarily through education and facilitating connections between affected individuals and medical professionals. They also aim to raise funds to promote extensive professional health education. Their ultimate objective is to uncover the causes of Proteus Syndrome, develop effective treatments, and ultimately discover a cure for this condition.
Official website here: www.proteus-syndrome.org
Who is the CEO of Proteus Syndrome Foundation?
Kim Hoag Green is the Executive Di of Proteus Syndrome Foundation.
Official website here: www.proteus-syndrome.org
What is the revenue of Proteus Syndrome Foundation?
Proteus Syndrome Foundation's revenue in 2022 was $90,842.
Official website here: www.proteus-syndrome.org
Who are the executives of Proteus Syndrome Foundation and what are their salaries?
There 25 volunteers at Proteus Syndrome Foundation.
Here are 10 key members and their salaries:
- Compensation: $20,000
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
- Compensation: $0
- Related: $0
- Other: $0
Official website here: www.proteus-syndrome.org
Where can I find the form 990 for Proteus Syndrome Foundation?
Proteus Syndrome Foundation's most recent form 990 was submitted in 2022 and can be accessed here.
Official website here: www.proteus-syndrome.org
Learn more at the official website: www.proteus-syndrome.org
Mission Statement of Proteus Syndrome Foundation
The Proteus Syndrome Foundation is committed to providing assistance to families affected by Proteus Syndrome. Their mission is threefold: firstly, they aim to educate individuals living with this condition and their families, fostering a sense of community and connecting them with other affected individuals and medical professionals. Secondly, the foundation is devoted to raising funds with the ultimate goal of advancing professional health education. Lastly, their ultimate objective is to uncover the causes, develop treatments, and eventually find a cure for Proteus Syndrome.
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Impact
October, 2024
The Proteus Syndrome Foundation has made a significant impact by providing essential support to families affected by Proteus Syndrome. Through education and networking opportunities, it connects individuals living with the condition to other families and medical professionals, fostering a sense of community and shared understanding. This foundation also actively raises funds to enhance professional health education, crucial for driving research aimed at understanding the cause of Proteus Syndrome, developing effective treatments, and ultimately finding a cure. Its commitment to empowering families and advancing medical knowledge plays a vital role in improving the lives of those impacted by this rare condition.
This information is meant to be a general summary of Proteus Syndrome 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.
- Investment Income: $3,194
- Gross Receipts: $108,599
Assets and Liabilities:
- Total Assets: $191,330
- Total Liabilities: $2,212
- Net Assets: $189,118
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Organization Details
Founding Year
1993
Phone
(901) 756-9375Principal Officer
Kim Hoag Green
Main Address
8485 DULWICH ROAD, CORDOVA, TN, 38016
Website
www.proteus-syndrome.orgNTEE Category
Code: T99Z - Philanthropy
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