Overview
What is Turner Syndrome Society Of The United States?
The Turner Syndrome Society of the United States (TSSUS), based in Houston, Texas, is a dedicated nonprofit organization focused on Turner Syndrome (TS). They offer a range of programs, including organizing national events for individuals with TS and their families, creating and maintaining TS content and resources, connecting people to relevant information, sustaining a research registry and professional provider directory, and raising TS awareness. In 2021, they supported over 2,500 individuals, managed 20 support groups, attracted 84,000 unique website visitors, and engaged 500+ attendees in 52 webinars. TSSUS advances knowledge, facilitates research, and provides support for all individuals impacted by Turner Syndrome, reaching out to approximately 75,000 people during Awareness Month. With a team of three dedicated employees, TSSUS is committed to making a difference in the lives of those with Turner Syndrome.
Official website here: www.turnersyndrome.org
Is Turner Syndrome Society Of The United States legitimate?
Turner Syndrome Society Of The United States is a legitimate nonprofit organization registered as a 501(c)(3) entity. Turner Syndrome Society Of The United States 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: $90,492
Professional Fundraising Fees: $0
Other Salaries and Wages: $106,744
For more financial information, click here
Official website here: www.turnersyndrome.org
What is the mission statement of Turner Syndrome Society Of The United States?
The Turner Syndrome Society of the United States (TSSUS) is dedicated to advancing knowledge, facilitating research, and providing support for individuals impacted by Turner Syndrome. Their mission encompasses organizing events, creating and maintaining resources, connecting people to information, sustaining research registries, and fostering professional provider directories. Through these efforts, they aim to increase awareness and provide assistance to over 2,500 individuals annually, as well as support various groups and reach a wide online audience. In 2021, they also facilitated 9 Turner Syndrome research studies.
Official website here: www.turnersyndrome.org
Who is the CEO of Turner Syndrome Society Of The United States?
Cindy C Scurlock is the Director of Turner Syndrome Society Of The United States. The CEO's salary of Turner Syndrome Society Of The United States is $90,492 and their total compensation is $90,492.
Official website here: www.turnersyndrome.org
What is the revenue of Turner Syndrome Society Of The United States?
Turner Syndrome Society Of The United States's revenue in 2022 was $522,013.
Official website here: www.turnersyndrome.org
Who are the executives of Turner Syndrome Society Of The United States and what are their salaries?
The average compensation at Turner Syndrome Society Of The United States during 2022 was $65,745. There are 3 employees and 50 volunteers at Turner Syndrome Society Of The United States.
Here are 11 key members and their salaries (Turner Syndrome Society Of The United States's CEO's salary is $90,492 and their total compensation is $90,492):
- Cindy C Scurlock (President & Ceo)
- Kristen Mckenney (Director)
- Laura Wuertele (Director)
- Christine Haley (Director)
- Sarah Bauer (Director)
- Kimberly Walker-Vanover (Director)
- Janine Reyes (Director)
- Jennifer Steele (Director)
- Brittani Laski (Board Chair) [Trustee/Director]
- Jeanna Lee (Board Chair Elect) [Trustee/Director]
- Daniel Tomkins (Treasurer) [Trustee/Director]
Official website here: www.turnersyndrome.org
Where can I find the form 990 for Turner Syndrome Society Of The United States?
The Turner Syndrome Society Of The United States’s most recent form 990 was submitted in 2022 and can be accessed here
Official website here: www.turnersyndrome.org
Learn more at the official website: www.turnersyndrome.org
Mission Statement of Turner Syndrome Society Of The United States
The Turner Syndrome Society of the United States (TSSUS) is dedicated to advancing knowledge, facilitating research, and providing support for all individuals impacted by Turner Syndrome. This esteemed organization plays a crucial role in promoting understanding and offering assistance to those affected by this condition.
In executing its mission, TSSUS organizes national events targeted at individuals with Turner Syndrome and their families. These events serve as platforms for fostering a sense of community and sharing experiences. Additionally, the society maintains and curates Turner Syndrome-related content and resources, connecting individuals to vital information. TSSUS also manages the Turner Syndrome Research Registry and a Professional Provider Directory, ensuring that researchers and healthcare providers have access to valuable data and resources. Moreover, the society raises awareness of Turner Syndrome through various channels, reaching out to an estimated 75,000 people during Awareness Month alone.
Furthermore, TSSUS supports 20 Turner Syndrome support groups and attended by 500+ individuals in 52 webinars in 2021. The society also reached out to 84,000 unique website visitors and boasts over 15,000 Facebook followers. These efforts underscore TSSUS's commitment to providing support, resources, and community for individuals affected by Turner Syndrome. In summary, the Turner Syndrome Society of the United States serves as a beacon of hope and support for individuals and families impacted by Turner Syndrome, working tirelessly to advance knowledge, facilitate research, and provide much-needed resources and connections.
Impact
This information is meant to be a general summary of Turner Syndrome Society Of The United States. Please take the time to review official sources before making any decisions based upon the content provided here.
Wednesday, July 24, 2024
The Turner Syndrome Society of the United States (TSSUS) impacts thousands of individuals by advancing knowledge, facilitating research, and providing support for all persons touched by Turner Syndrome. In 2021 alone, TSSUS supported 2,500 individual requests for help, organized national Turner Syndrome events for those affected and their families, sustained the Turner Syndrome research registry and professional provider directory, and created awareness about Turner Syndrome. Additionally, TSSUS hosted 20 support groups, reached 84,000 unique website visitors, engaged with 15,000 Facebook followers, and had over 500 attendees in 52 webinars. The organization also supported 9 Turner Syndrome research studies and reached 75,000 people during Turner Syndrome Awareness Month. Through these efforts, TSSUS plays a vital role in providing resources, connections, and support for individuals and families impacted by Turner Syndrome.
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.
VIRTUAL/ANNUAL EVENTS
Revenue
$10,440
Organization Details
Founding Year
2001
Phone
(832) 912-6006
Principal Officer
Cindy C Scurlock
Main Address
11250 WEST ROAD SUITE G, HOUSTON, TX, 77065
Website
www.turnersyndrome.org
NTEE Category
Code: G20 - Disease
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