The Federation was founded in 2012 as a result of the strong commitment of its promoters by bringing together the largest number of people affected, integrating not only those who have the disease, but also his whole family. It is true that, due the competences transferred to the autonomous communities, existing reginonal public services are different. For the Federation, one of our objectives is to optimize these services for a comprehensive treatment of those affected, and avoid just grievances that may occur between different regions.