DSRCT is rare but support shouldn't be. Every purchase grows DSRCT awareness and community.
Shop to Show Your Support
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.
AWARENESS DESIGNS
FOR AND BY
THE DSRCT COMMUNITY
Meet one of the Artists:
Gianna Cericola
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.
Why The DSRCT Initiative Exists
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.
Join us
You do not have to do this alone.
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.
FOLLOW THE DSRCT INITIATIVE ON SOCIALS
for Awareness Content, Lived Experience Stories, and Community
