Platelet Disorder Support Association

The Platelet Disorder Support Association (PDSA) is dedicated to enhancing the lives of people with immune thrombocytopenia (ITP) and other platelet disorders through education, advocacy, research and support. PDSA connects ITP patients and caregivers with life-altering programs and support. We serve as a powerful force educating and unifying the global ITP community of patients, caregivers, practitioners and key disease stakeholders and proudly serve as a trusted resource for the scientific community. Our comprehensive offering of programs and services not only empowers patients to better understand and take control of their disease, but also enables clinicians to stay current on the latest ITP protocols, cutting-edge research and innovative therapies being developed worldwide, so clinicians can remain focused on exceptional patient care. PDSA is committed to building awareness, educating the global community, and providing critical connections and resources that empower patients to take charge of their disease and encourage practitioners to exercise patient-centered medical care. PDSA collaborates with other patient advocacy groups, researchers, and government agencies to drive public policy, develop new treatment options and support research to find a cure. PDSA’s Research Program supports investigators conducting innovative ITP patient-centered research. The PDSA ITP Registry collects patient-consented data on the natural progression of ITP. Patient-founded, PDSA’s leadership continues through a personal connection to ITP and a small but mighty staff dedicated to championing the cause. Our Medical Advisory Board is comprised of world-renowned hematological experts from leading academic and medical institutions who provide insight, direction and expertise to our organization and our Board of Directors represent the broad diversity of our membership and contribute their time, talent, and passion to further our mission.... More Info Less Info