RRP, the Platelet Disorder Support Association (PDSA) and the Foundation for Women and Girls with Blood Disorders (FWGBD) co-hosted this clinical practice webinar around correctly diagnosing ITP.

Joy Anderson, mother and wife of RUNX1-FPD patients, and Christina Timleck, RUNX1-FPD patient, daughter and mother, shared their experiences with years-long challenges to arrive at accurate diagnoses.

Katie Bergstrom, a genetic counselor at Seattle Children’s Hospital, presented on “Genetic Counseling and Testing Considerations” and Dr. Michele Lambert, Medical Director of the Special Coagulation Laboratory at Children’s Hospital of Philadelphia and a PDSA Medical Advisor, shared ways to determine “Is It Really ITP?”