Friends for Research

The PND association is a disease organization representing children and families who are affected by a pediatric neurotransmitter disease.

As a rare disease advocacy organization our mission is to represent and be a voice for all children affected by dopamine related PND's. Our goals are to help children and families who are affected by PND's, support the identification of new PND's, find better treatments and ultimately a cure for those diseases that are already known. The PND Association was founded in 1998 and is a non-profit, voluntary organization.

All information contained on the PND Association website is intended for informational and educational purposes. The information is not intended to be a replacement or substitute for professional medical treatment or for professional medical advice relative to a specific medical question or condition.