Overview
What is Pten Hamaratoma Syndrome Foundation?
The Pten Hamartoma Syndrome Foundation is a dedicated nonprofit organization committed to combating Pten Syndromes. Their primary goal is to fund research to discover potential treatments and therapies, while simultaneously offering education on PHTS to the public. They also support affected individuals and work tirelessly to increase awareness about Pten Hamartoma Tumor Syndrome, encompassing conditions such as Cowden Syndrome, Bannayan-Riley-Ruvalcaba Syndrome, Pten-Related Proteus Syndrome, and Proteus-Like Syndrome. Furthermore, they financially support associated research centers and organizations to further their investigation into Pten Hamartoma Tumor Syndromes.
Official website here: www.ptenfoundation.org
What do the Facebook reviews say about Pten Hamaratoma Syndrome Foundation?
100% of reviewers on Facebook recommend the Pten Hamaratoma Syndrome Foundation. Here is a summary of their reviews: The foundation is praised for its organization and the quality of its events and initiatives. Many appreciate the thoughtful, passionate, and skilled leadership behind the organization.
Supporters feel a strong connection to the foundation's mission and express satisfaction with its ability to deliver meaningful experiences. The commitment to the community and the effective management of resources also receive commendations.
Overall, those who engage with the Pten Hamaratoma Syndrome Foundation convey a sense of pride and confidence in its efforts, highlighting the positive impact it has on raising awareness and supporting individuals affected by the syndrome.
This AI summary has been generated from reviews found on Facebook.
Is Pten Hamaratoma Syndrome Foundation legitimate?
Pten Hamaratoma Syndrome Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. Pten Hamaratoma Syndrome 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.
Official website here: www.ptenfoundation.org
What is the mission statement of Pten Hamaratoma Syndrome Foundation?
The Pten Hamaratoma Syndrome Foundation strives to advance treatments or therapies for Pten Syndromes by funding relevant research. They are dedicated to spreading awareness about Pten Hamartoma Tumor Syndrome, which includes conditions such as Cowden Syndrome, Bannayan-Riley-Ruvalcaba Syndrome, Pten-Related Proteus Syndrome, and Proteus-Like Syndrome. The foundation also provides educational resources to support patients and increases public understanding of these syndromes. Furthermore, they financially support associated research centers and organizations, contributing to the advancement of knowledge about Pten Hamartoma Tumor Syndromes.
Official website here: www.ptenfoundation.org
Who is the CEO of Pten Hamaratoma Syndrome Foundation?
Kristin Anthony is the President of Pten Hamaratoma Syndrome Foundation.
Official website here: www.ptenfoundation.org
What is the revenue of Pten Hamaratoma Syndrome Foundation?
Pten Hamaratoma Syndrome Foundation's revenue in 2022 was $61,272.
Official website here: www.ptenfoundation.org
Who are the executives of Pten Hamaratoma Syndrome Foundation and what are their salaries?
Here are 3 key members and their salaries:
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Official website here: www.ptenfoundation.org
Where can I find the form 990EZ for Pten Hamaratoma Syndrome Foundation?
Pten Hamaratoma Syndrome Foundation's most recent form 990EZ was submitted in 2022 and can be accessed here.
Official website here: www.ptenfoundation.org
Learn more at the official website: www.ptenfoundation.org
Mission Statement of Pten Hamaratoma Syndrome Foundation
The Pten Hamartoma Syndrome Foundation is devoted to seeking effective treatments and therapies for various Pten Syndromes. This nonprofit organization accomplishes this goal by funding research, disseminating knowledge about Pten Hamartoma Tumor Syndrome, and offering support to affected individuals. The syndromes the foundation focuses on include Cowden Syndrome, Bannayan-Riley-Ruvalcaba Syndrome, Pten-Related Proteus Syndrome, and Proteus-Like Syndrome.
In addition to funding research, the Pten Hamartoma Syndrome Foundation invests in associated research centers and organizations. By providing grants, this nonprofit organization contributes to the advancement of scientific understanding and potential solutions for Pten Hamartoma Tumor Syndromes.
Furthermore, the foundation plays a crucial role in raising awareness about these syndromes. By educating the public, they aim to foster understanding and support for individuals living with these conditions. This mission extends to empowering patients, offering them a community in which to share experiences and seek advice. As such, the Pten Hamartoma Syndrome Foundation is dedicated to making a significant impact in the lives of those affected by these syndromes.
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Impact
August, 2024
The Pten Hamartoma Syndrome Foundation's impact is significant in the field of healthcare and rare genetic disorders. By funding research, providing education about Pten Syndromes, supporting patients, and raising awareness, the foundation is actively contributing to the search for treatments or therapies for Pten Syndromes. Through its efforts, the foundation is increasing awareness of Pten Hamartoma Tumor Syndrome, which includes rare conditions like Cowden Syndrome, Bannayan-Riley-Ruvalcaba Syndrome, Pten-Related Proteus Syndrome, and Proteus-Like Syndrome. Moreover, by granting funds to associated research centers and organizations, the foundation is directly supporting research efforts to better understand and address Pten Hamartoma Tumor Syndromes. This dedication and focus have a positive and profound impact on individuals affected by these rare disorders and the medical community as a whole.
This information is meant to be a general summary of Pten Hamaratoma 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: $262
- Gross Receipts: $61,272
Assets and Liabilities:
- Total Assets: $135,587
- Total Liabilities: $27,917
- Net Assets: $107,670
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Organization Details
Phone
(256) 533-5850Principal Officer
Kristin Anthony
Main Address
2325 LITTLE COVE ROAD, HAMPTON COVE, AL, 35763
Website
www.ptenfoundation.orgNTEE Category
Code: E86 - Health
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