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Kate Foundation For Rett Syndrome Research Inc

Learn about this cause: Is it Legit? Do I like the mission? What is the CEO's salary?

EIN: 271218153 ✦ Old saybrook, CT ✦ Designated as a 501(c)(3)

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Overview

What is Kate Foundation For Rett Syndrome Research Inc?

The Kate Foundation for Rett Syndrome Research Inc is a nonprofit organization committed to increasing awareness about Rett Syndrome and related mecp2 disorders. Its primary goal is to champion scientific research aimed at reversing the effects of Rett Syndrome and alleviating its symptoms. By promoting scientific exploration in this field, the foundation seeks to make a significant impact on the lives of those affected by these disorders. The foundation's activities and mission are centered around raising awareness, supporting research, and advocating for advancements in the understanding and treatment of Rett Syndrome.


Official website here: www.katefoundation.org

Is Kate Foundation For Rett Syndrome Research Inc legitimate?

Kate Foundation For Rett Syndrome Research Inc is a legitimate nonprofit organization registered as a 501(c)(3) entity. Kate Foundation For Rett Syndrome Research Inc 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.katefoundation.org

What is the mission statement of Kate Foundation For Rett Syndrome Research Inc?

The Kate Foundation for Rett Syndrome Research Inc is committed to increasing public understanding of Rett Syndrome and related mecp2 disorders. Their primary objective is to foster and endorse scientific research aimed at reversing the effects of Rett Syndrome and alleviating its symptoms. By doing so, they strive to provide relief and support to those affected by this disorder. The foundation's activities primarily revolve around advocating for and funding research initiatives that hold promise for advancing treatments and ultimately finding a cure for Rett Syndrome.


Official website here: www.katefoundation.org

Who is the CEO of Kate Foundation For Rett Syndrome Research Inc?

Jeffrey J Canavan is the President of Kate Foundation For Rett Syndrome Research Inc.


Official website here: www.katefoundation.org

What is the revenue of Kate Foundation For Rett Syndrome Research Inc?

Kate Foundation For Rett Syndrome Research Inc's revenue in 2022 was $37,558.


Official website here: www.katefoundation.org

Who are the executives of Kate Foundation For Rett Syndrome Research Inc and what are their salaries?


Here are 2 key members and their salaries:


Jeffrey J Canavan (President)
  • Compensation: $0
  • Related: $0
  • Other: $0
Sarah S Canavan (Secretary)
  • Compensation: $0
  • Related: $0
  • Other: $0


Official website here: www.katefoundation.org

Where can I find the form 990EZ for Kate Foundation For Rett Syndrome Research Inc?

Kate Foundation For Rett Syndrome Research Inc's most recent form 990EZ was submitted in 2022 and can be accessed here.


Official website here: www.katefoundation.org

Learn more at the official website: www.katefoundation.org

Mission Statement of Kate Foundation For Rett Syndrome Research Inc

The Kate Foundation for Rett Syndrome Research Inc is committed to raising awareness about Rett Syndrome and related mecp2 disorders. Their primary mission is to foster and promote scientific research aimed at reversing the effects of Rett Syndrome and alleviating its symptoms. By doing so, they strive to improve the lives of those affected by this condition and contribute to the broader medical community's understanding of associated disorders. The foundation's efforts are geared towards advancing knowledge and treatments, ultimately working towards a future where Rett Syndrome no longer poses a significant challenge to those living with it.

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Impact




August, 2024

The impact of the Kate Foundation For Rett Syndrome Research Inc is focused on raising awareness of Rett Syndrome and other mecp2 disorders, as well as supporting and promoting scientific research aimed at reversing Rett Syndrome and relieving its symptoms. This organization plays a vital role in advocating for those affected by Rett Syndrome and driving research efforts towards finding potential treatments and cures for this debilitating condition. Through their activities and initiatives, the Kate Foundation strives to make a significant difference in the lives of individuals and families impacted by Rett Syndrome.




This information is meant to be a general summary of Kate Foundation For Rett Syndrome Research Inc. 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.

Revenue
$37,558 (2022)
Expenses
$39,000 (2022)
Efficiency

Other financial information:

This information is from the most recently submitted tax form from this organization, which was in 2022.

  • Investment Income: $2
  • Gross Receipts: $37,558

Assets and Liabilities:

  • Total Assets: $42,578
  • Total Liabilities: $130
  • Net Assets: $42,448

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Organization Details

Principal Officer

Jeffrey J Canavan

Main Address

PO BOX 213, OLD SAYBROOK, CT, 06475

NTEE Category

Code: H112 - Medical research

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