In the summer of 2013, BBDF presented the first in what will be a series of webinars on JNCL designed for foundations, parents, family and loved ones of those affected by Batten. The webinars are a platform for us to share the latest information on juvenile Batten disease research and provide a forum for information sharing. This 30 minute webinar allows us to describe our strategy as it relates to finding a treatment and cure for juvenile Batten disease. We talk about the global efforts in JNCL research and how all the pieces fit together to get a treatment as quickly and inexpensively as possible. This first presentation gives a broad overview of our strategy and we will provide more detailed information in the webinars to follow.