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Chondrosarcoma CS Foundation, Inc.

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    Uncategorized Posts

    The First Twerk Walking Out Of The Hospital After Kicking Cancer’s Ass Has To Be The Sweetest

    March 23rd, 2023
    Some of you may not know who Amber Sarcone is. In Philly, she’s a part of the royal family. Her family runs Sarcone’s Bakery, makers of some of the most delicious damn bread you’ll ever have the pleasure of shoving into your mouth. Her cousin is…

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    Revolutionary new bone cancer drug identified

    March 16th, 2023
    A research team led by Dr Darrell Green, a trustee of the Bone Cancer Research Trust, have identified a new drug that works against all main forms of bone cancer. Researchers at the University of East Anglia discovered that the drug, called…

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    Recruitment Efforts Underway for the Chondrosarcoma Patient Registry

    March 15th, 2023
    The Chondrosarcoma Foundation in partnership with the National Organization for Rare Disorders (NORD®) has launched the Chondrosarcoma Patient Registry. The patient registry creates a platform for patients around the world to strengthen their…

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    Join us on Tuesday Night to Address Care to Treat Chondrosarcoma

    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…

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    New Patient Registry Creates A Platform to Share Patient Journeys with Chondrosarcoma

    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…

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    Rare Disease Day 2023: Empowering Community Advocacy And Innovation

    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…

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    Join the CS Foundation Patient / Caregiver / Family Advisory Board

    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…

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    In Three Days: February 6: Chondrosarcoma Awareness Day

    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/

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    Remember the Contributions of David Bowles

    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…

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    Genomic profiling identifies genes and pathways dysregulated by HEY1-NCOA2 fusion and shines a light on mesenchymal chondrosarcoma tumorigenesis

    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…

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    If you would like to learn more about CS Foundation or if you would like to learn more about the resources we provide to patients, families, caregivers, and physicians, please contact us by phone or send us a message.

    **A Registered 501c3 Non-Profit Charity Organization. All donations are tax-deductible.**

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