DSRCT is rare but support shouldn't be. Every purchase grows DSRCT awareness and community.
Browse items designed by the DSRCT community to spread awareness and encourage meaningful support for families in the fight against DSRCT. Proceeds support The DSRCT Initiative.

Hi, I’m Gianna. I’m a graphic designer and content creator sharing my journey with DSRCT.
Diagnosed in October 2024 at the age of 27, I am now 29 and I’ve been NED (no evidence of disease) since June 2025, and I use my platform to raise awareness, inspire others facing this diagnosis, and offer hope.
Through my content, I show that a diagnosis doesn’t define the whole story. There is always hope and you are not alone.

To unite all who are impacted by Desmoplastic Small Round Cell Tumor (DSRCT) through community, awareness, accessible disease information, and support, in pursuit of a world where no one faces this disease alone or without hope.
Our peer support community is a free weekly resource for patients and caregivers. Come exactly as you are. You are not alone. We are stronger together.

