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 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 2000 and is a non-profit, voluntary organization.

Advisory Board

Review our domestic and international advisory board for the PND association

Board of Directors

The PND Association is governed by a volunteer Board of Directors. The board serves as the principal decision-making body.

Contact Us

Contains the names and contact information for point people at the PND Association.


Accomplishments of the PND Association from 1998 to current.