Overview
What is Smith-Lemli-Opitz Foundation?
The Smith-Lemli-Opitz Foundation is a charitable organization, headquartered in Fargo, North Dakota, dedicated to serving families impacted by Slo Syndrome. Established in 1988 with a small group of 37 families, the foundation's mission has since expanded to support over 500 families worldwide. Its primary objective is to fund research studies on Smith-Lemli-Opitz Syndrome, aiming to gain a deeper understanding of the condition. Simultaneously, the foundation provides vital information to these families, fostering a sense of community and mutual support. By offering grants and resources, the Smith-Lemli-Opitz Foundation seeks to enhance the lives of those affected by this syndrome.
Official website here: www.smithlemliopitz.org
Is Smith-Lemli-Opitz Foundation legitimate?
Smith-Lemli-Opitz Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. Smith-Lemli-Opitz Foundation submitted a form 990EZ, 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
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Official website here: www.smithlemliopitz.org
What is the mission statement of Smith-Lemli-Opitz Foundation?
The Smith-Lemli-Opitz Foundation's mission is centered around supporting families affected by Slo Syndrome. This is accomplished through its primary objective of raising funds for research into the condition. The foundation provides grants for studying Smith-Lemli-Opitz Syndrome and offers informational resources to these families. Originally established by a group of 37 families in 1988, the organization has since expanded to assist over 500 families. Its mission is to offer a platform for these families to exchange experiences and information, thereby fostering a sense of community and support.
Official website here: www.smithlemliopitz.org
Who is the CEO of Smith-Lemli-Opitz Foundation?
Gretchen Noah is the President of Smith-Lemli-Opitz Foundation.
Official website here: www.smithlemliopitz.org
What is the revenue of Smith-Lemli-Opitz Foundation?
Smith-Lemli-Opitz Foundation's revenue in 2022 was $59,374.
Official website here: www.smithlemliopitz.org
Who are the executives of Smith-Lemli-Opitz Foundation and what are their salaries?
- Gretchen Noah (President)
- Kate Duren (Director)
- Kelly Noah (Secretary)
- Caroline Kelly (Director)
- Kayleigh Kempster (Director)
- Carola Gutierrez (Director)
- Celia Trimestra (Director)
- Michael Cohen (Director)
- Amy Dinunzio (Director)
Official website here: www.smithlemliopitz.org
Where can I find the form 990EZ for Smith-Lemli-Opitz Foundation?
The Smith-Lemli-Opitz Foundation’s most recent form 990EZ was submitted in 2022 and can be accessed here
Official website here: www.smithlemliopitz.org
Learn more at the official website: www.smithlemliopitz.org
Mission Statement of Smith-Lemli-Opitz Foundation
The Smith-Lemli-Opitz Foundation, a nonprofit organization established in 1988, is dedicated to supporting families impacted by Slo Syndrome. Its primary objective is to raise funds for research grants, aimed at advancing the understanding of Smith-Lemli-Opitz Syndrome. Alongside this, the foundation serves as a resource, providing families with essential information about the condition. Initially, the organization began as a small network of 37 families sharing experiences and knowledge. Since then, it has grown significantly, now assisting over 500 families affected by Slo Syndrome. The Smith-Lemli-Opitz Foundation's mission is to offer a supportive environment, fostering understanding, and facilitating research advancements in the field of Slo Syndrome.
Impact
This information is meant to be a general summary of Smith-Lemli-Opitz Foundation. Please take the time to review official sources before making any decisions based upon the content provided here.
Sunday, August 4, 2024
The Smith-Lemli-Opitz Foundation's impact is significant in providing support services to families affected by Smith-Lemli-Opitz Syndrome (SLO). By raising funds to provide research grants for the study of SLO and offering information to families, the foundation plays a crucial role in improving the lives of individuals with this rare genetic condition. Originally founded by a group of 37 families with SLO children in 1988, the foundation has since grown to support over 500 families, making a difference in the SLO community.
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:
Organization Details
Phone
(701) 367-1976
Principal Officer
Gretchen Noah
Main Address
PO BOX 10598, FARGO, ND, 58106
Website
www.smithlemliopitz.org
NTEE Category
Code: A99Z - Arts
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