The majority of funds raised by Casey’s Cause will be given to the Platelet Disorders Support Association (“PDSA”).  PDSA is a non-profit organization with an extensive support network for patients and family members of patients with ITP.  They have recently created a research fund to which we will make donations, ensuring the best usage of our funds towards children’s research efforts.  We, the board of Casey’s Cause, believe that creating our own organization (rather than by simply donating our own personal funds to an organization such as PDSA) will provide opportunities for us to make a greater difference in the lives of those affected by ITP.  We are fortunate to have on our board two nurses and a pharmacist who hope to become certified to hold continued education seminars on ITP for medical professionals.  Members of our board also plan to visit area schools and other community groups to conduct informative classes for teachers, school nurses and other interested individuals relating to them the symptoms and treatment of ITP in children. The remainder of the funds raised is to be used for educational programs, as well as for assisting with the needs of patients and families affected by ITP.  The primary recipient being Camp Charley's camp held for children with ITP and their families.  Casey’s Cause will continue to meet frequently in order to identify all areas of need.