Education:
To provide information and educational resources to the lay public and to health care providers in order to promote early diagnosis and treatment.

Research:
To encourage and to fund research on the Long QT Syndrome and other genetic cardiac diseases predisposing the young to sudden death.

Resource Services:
To serve as a patient referral resource and to provide information to physicians who care for patients with arrhythmia disorders.

Geneology Information:
To identify individuals and families by pedigree development and support diagnostic testing where appropriate.

Family Support:
To assist families and friends of those affected by the Long QT Syndrome and other arrhythmia disorders.