People who suffer from Prader Willi Syndrome (PWS) suffer serious difficulties every day of their lives, with important complications that extend to each of the vital functions that make up the human being and that generate a peculiar existence.
The educational, social and work development of a person diagnosed with this syndrome is a path that they will never be able to travel alone, since a large part of the symptoms they suffer will require the support and / or vigilance of another adult who takes responsibility for their health and behaviour. It is a genetic alteration that mainly affects the central nervous system. The influence of this disorder on the body is irreversible and extensive, with development at a physical, psychological and social level being seriously compromised.
Those affected by PWS do not receive the signal of nutritional satiety and suffer from a continuous urge to eat, risking their lives many times to find food. In addition, the disease causes sleep disorders, breathing and body temperature problems, incomplete development of sexual characteristics, learning and language problems, and very serious behavior problems.
Given the unique complexity, which decisively influences the physical and psychological development of those who suffer from this disease for life, the only possible conclusion is that the creation of a specific residence for people with this disorder is essential. The bibliography and experience show that good management of environmental variables can favor the quality of life of people with Prader Willi Syndrome and, of course, that of their relatives. In Spain there is still no center of these characteristics.