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Leading the Fight to treat and cure
Tay-Sachs, Canavan, Sandhoff, GM1 and related diseases

Honoring Kit

 

Kit Payette 

March 15, 2014 - December 16, 2016

"Life off Earth is in two important respects not at all unworldly: you can choose to focus on the surprises and pleasures, or the frustrations. And you can choose to appreciate the smallest scraps of experience, the everyday moments, or to value only the grandest, most stirring ones."

- Chris Hadfield, An Astronaut's Guide to Life on Earth

Your gifts will honor and extend Kit's legacy through the support of future developments in Sandhoff research and the NTSAD Annual Family Conference experience. The Payettes were able to attend the 2016 NTSAD Annual Family Conference, and felt that they greatly benefited from meeting and getting to know other families like them. In honor of their daughter Kit they would like to give back and make it possible for other families to experience the same support.  Thank you, on behalf of Kit's family - Leslie, Bruno and Posie.  

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What is Sandhoff?

Sandhoff is a lysosomal storage disorder. It is caused by a mutation in the gene responsible for the vital enzymes called beta hexaminidase A and B. The role of these enzymes is to degrade a fatty substance or lipid called GM-2 ganglioside. In the absence of the enzymes, GM-2 accumulates abnormally in cells, especially in the nerve cells, or neurons, of the brain. This ongoing accumulation, or "storage", of GM-2 causes progressive damage and eventually death of the cells.

What about research?

Sandhoff Disease research is usually performed simultaneously with Tay-Sachs disease research. This is because these two diseases have a similar underlying biochemical mechanism.

Read more about the Research We Fund here.

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