Our Foundation has been established to eliminate the life-threatening PLN heart disease p.Arg14del. This genetic disorder causes heart diseases (cardiomyopathies, arrhythmias…) whereby the pump function of the heart muscle is significantly defective. PLN gene carriers are burdened with serious heart failure problems which may lead to a heart transplant, ventricular assist devices or even sudden premature death. Our Foundation has been established by volunteers or people suffering from PLN, family members and their loved ones, and tries to inform PLN gene carriers as much as possible about the latest developments and PLN studies. We also can establish contact between fellow PLN sufferers in order to share their own experiences and dilemmas… because we all are family and supporting each other is important in this disease process!