News

FOR IMMEDIATE RELEASE
Contact:
Sue Martin, Executive Director
Bleeding Disorders Association of South Carolina
Phone: (864) 350-9941
Email: sue.martin@bda-sc.org

 

 

Greenville, SC – [September 22, 2025] – The Bleeding Disorders Association of South Carolina (BDASC) is proud to announce the return of its premier fundraising event, the Par Fore The Clot Charity Golf Tournament, on Friday, September 26, 2025, at the Preserve at Verdae Golf Club in Greenville, South Carolina.

 

Now in its 11th year, this exciting annual tournament unites community leaders, advocates, and golf enthusiasts for a day of friendly competition, fun, and philanthropy—all in support of South Carolinians living with bleeding disorders such as hemophilia and von Willebrand disease.

 

Proceeds from the event directly support BDASC’s mission to improve the quality of life for individuals and families through advocacy, research awareness, access to care, and education about promising therapies such as gene therapy. These funds also sustain programs that raise public awareness of bleeding disorders and ensure that the voices of patients and caregivers are heard at the state and national level.

 

“Par Fore The Clot is more than a tournament—it’s a platform for advocacy and progress,” says Samantha Javorka, Engagement & Development Manager of BDASC. “Your support helps us drive awareness, advance research opportunities, and empower our community to navigate life-changing treatments like gene therapy. Beyond financial assistance and scholarships, this event strengthens our ability to stand up for access to care and policies that protect those living with bleeding disorders.”

 

The day will include:

 

For more information, visit www.bda-sc.org, follow us on Instagram @hemoofsc, or contact Sue Martin, Executive Director, at (864) 350-9941 or sue.martin@bda-sc.org

 

 

The Bleeding Disorders Association of South Carolina (BDASC) is a 501(c)(3) nonprofit organization dedicated to advocacy, education, research awareness, and support for individuals and families affected by hemophilia, von Willebrand disease, and other rare bleeding disorders. BDASC empowers the community through programs that promote access to care, elevate awareness of emerging therapies like gene therapy, and ensure that patient voices are represented in policy decisions. BDASC is a proud chapter of the Hemophilia Federation of America and a member organization of the National Bleeding Disorders Foundation.