March 5th, 2023

The Chondrosarcoma Foundation is developing a Patient / Family/ Caregiver Advisory Board in the effort to create a voice for chondrosarcoma patient’s and caretakers to address concerns and advocate for effective treatment and quality care.

The…

March 2nd, 2023

The Chondrosarcoma Foundation in partnership with the National Organization for Rare Disorders (NORD®) has launched the Chondrosarcoma Patient Registry. Chondrosarcoma is a rare bone cancer that currently has no cure. Its prevalence and origin are…

February 24th, 2023

The time has come to make rare diseases a national public health imperative For decades, the rare disease community has been striving for greater recognition and scientific breakthroughs addressing the unmet medical needs millions of Americans face…

February 20th, 2023

The Chondrosarcoma Foundation is developing a Patient / Caregiver / Family Advisory Board in the effort to create a voice for the chondrosarcoma community to address concerns and advocate for effective treatment and quality care.

The advisory board…

February 3rd, 2023

Join the Fight

Wear A Yellow Ribbon on Monday, February 6. Post Your Picture to #CSWECARE

Sign Our Petition for more Clinical Trials: www.csfshayna.org/support-cs-research/

January 29th, 2023

We are just one week away from hosting Chondrosarcoma Awareness Day on February 6 (Shayna’s heavenly 32nd birthday). This is our international effort to educate the public about this rare bone cancer and to build a coalition to support more…

January 24th, 2023

Abstract

Mesenchymal chondrosarcoma is a rare, high-grade, primitive mesenchymal tumor. It accounts for around 2-10% of all chondrosarcomas and mainly affects adolescents and young adults. We previously described the HEY1-NCOA2 as a recurrent gene…

January 22nd, 2023

We are just two weeks away from hosting Chondrosarcoma Awareness Day on February 6 (Shayna’s heavenly 32nd birthday). This is our international effort to educate the public about this rare bone cancer and to build a coalition to support more…

January 10th, 2023

We are just four weeks away from hosting Chondrosarcoma Awareness Day on February 6 (Shayna’s heavenly 32nd birthday). This is our international effort to educate the public about this rare bone cancer and to build a coalition to support more…

January 7th, 2023

A genetic model for central chondrosarcoma evolution correlates with patient outcome William Cross 1, Iben Lyskjær 1 2, Tom Lesluyes 3, Steven Hargreaves 1, Anna-Christina Strobl 4, Christopher Davies 1 4, Sara Waise 3 5, Shadi Hames-Fathi 1,…