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        <ExplanationTxt>THE PURPOSE OF CS FOUNDATION IS TO EDUCATE THE PUBLIC ABOUT CHONDROSARCOMA; SUPPORT AND ADVOCATE FOR PATIENTS AND FAMILIES THAT ARE SUFFERING FROM THIS DISEASE, AND ADVOCATE TO IMPROVE THE TREATMENT AND CARE FOR THESE PATIENTS. CS FOUNDATION ALSO STRIVES TO ADVOCATE AND PROMOTE POSITIVE CHANGES INCLUDING A VIABLE TREATMENT PROTOCOL, EARLY DETECTION, PROPER SURVEILLANCE, MORE EFFICIENT AND RELEVANT INFORMATION DEDICATED TO CHONDROSARCOMA, AS WELL AS CREATING NETWORKING OPPORTUNITIES FOR SARCOMA EXPERTS TO SPECIFICALLY ADDRESS CHONDROSARCOMA. MOST IMPORTANTLY, CS FOUNDATION STRIVES TO ADVOCATE FOR MORE COMPASSIONATE CARE, CUTTING THROUGH PHARMACEUTICAL RED-TAPE, AND PROMOTING THE PATIENTS RIGHT TO RECEIVE TREATMENT ESPECIALLY IF NEW SOLUTIONS ARE POTENTIALLY LIFE-SAVING.</ExplanationTxt>
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        <FormAndLineReferenceDesc>FORM 990, PAGE 1, PART I, LINE 6</FormAndLineReferenceDesc>
        <ExplanationTxt>COMMITTEE VOLUNTEERS</ExplanationTxt>
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        <FormAndLineReferenceDesc>FORM 990, PAGE 2, PART III, LINE 2</FormAndLineReferenceDesc>
        <ExplanationTxt>CHONDROSARCOMA PATIENT REGISTRY THE CHONDROSARCOMA FOUNDATION IN PARTNERSHIP WITH THE NATIONAL ORGANIZATION FOR RARE DISORDERS (NORD) HAS LAUNCHED THE CHONDROSARCOMA PATIENT REGISTRY. FINANCIAL SUPPORT FOR THE INITIAL DESIGN AND IMPLEMENTATION OF THE REGISTRY HAS BEEN PROVIDED BY INHIBRX, SERVIER, CSX TRANSPORTATION, AND DONATIONS FROM INDIVIDUALS AND FUNDRAISERS. THIS REGISTRY WILL COLLECT INFORMATION FROM PARTICIPANTS (OR THEIR LEGALLY AUTHORIZED REPRESENTATIVES) WHO ARE AFFECTED BY CHONDROSARCOMA. THE REGISTRY WILL ALSO COLLECT INFORMATION ON THOSE WHO HAVE PASSED, TO BE ENTERED BY AUTHORIZED REPRESENTATIVES.</ExplanationTxt>
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        <FormAndLineReferenceDesc>FORM 990, PAGE 2, PART III, LINE 4D</FormAndLineReferenceDesc>
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        <FormAndLineReferenceDesc>FORM 990, PAGE 6, PART VI, LINE 11B</FormAndLineReferenceDesc>
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