SMARCB1 Hope is a non-profit organization dedicated to finding effective treatments for
SMARCB1-deficient cancers
Together, let’s find a cure.
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About SMARCB1 Cancers
SMARCB1 cancers are aggressive, affect mostly children and young adults and lack effective treatments. They can appear at different ages and in different parts of the body, bear different names and have different pathologies and symptoms, but they are all driven by the loss of one single gene: SMARCB1. Knowledge among specialists the world over is limited and scattered. By joining forces, we can find a cure for these cancers and make a great leap forward in understanding the vital role of epigenetics in all cancer.
About Us
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We are a French-American family with four children. In 2020,
from one day to the next, our happy lives were turned upside down.
Our second child, Ella, was diagnosed with an incurable SMARCB1-deficient
sinonasal carcinoma (SDSC) at the age of 23.
What We Do
We foster a community of scientists, treating oncologists, patients, and families around all SMARCB1 cancers and support international collaborative research and new R&D approaches.
We shine a spotlight on SMARCB1-deficient sinonasal carcinoma (SDSC) and provide support and guidance to patients. Through sharing information, uniting research efforts, and connecting with one another, we will accelerate progress towards a cure for SMARCB1 cancers.
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Partnered with
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