Kate Foundation for Rett Syndrome Research Inc

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The Kate Foundation is a 501(c)(3) organization dedicated to raising research funding for the reversal of Rett Syndrome and related disorders. TO RAISE AWARENESS OF RETT SYNDROME AND OTHER MECP2 DISORDERS, AND TO SUPPORT AND PROMOTE SCIENTIFIC RESEARCH SEEKING THE REVERSAL OF RETT SYNDROME AND RELIEF OF RETT SYNDROME SYMPTOMS.

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271218153

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Old Saybrook

Address: PO Box 213, Old SaybrookWeb: Sign in to see organisation websiteX (Twitter): katefoundationRevenue: 25429ICO: 271218153

Kate Foundation for Rett Syndrome Research Welcome to the Kate Foundationfor Rett Syndrome Research The Kate Foundation for Rett Syndrome Research is a 501c3 nonprofit organization dedicated to raising funding for scientific research seeking the reversal of Rett Syndrome and the relief of Rett Syndrome symptoms. Funds raised by the Kate Foundation go to the Rett Syndrome Research Trust a501c3 nonprofit organization intensively focused on the development of treatments and cures for Rett Syndrome and related MECP2 disorders. Since 2009 the Kate Foundation has raised over 900000 for this research. Rett Syndrome is a neurological disorder caused by a mutation in a gene called MECP2.

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Cathy

💜 Every step taken towards understanding MECP2 is a step closer to hope for so many. Proud to support the Kate Foundation’s mission! #RettSyndromeAwareness

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Jessica

🌟 Amazing work being done by the Kate Foundation! Let’s continue to raise funds and support research to change lives. Together, we can make a difference! #CureRettSyndrome

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Sarah

1. What innovative fundraising strategies have been most effective for nonprofit organizations like the Kate Foundation in raising awareness and funds for Rett Syndrome research?

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Catherine

2. How can we enhance collaboration among different organizations focused on MECP2-related disorders to accelerate research and treatment breakthroughs?

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