Prader Willi Syndrome Awareness Month

Prader Willi Syndrome is a rare genetic disorder that affects nearly every body system but is most famously known for causing extreme, continuous hunger along with a slow metabolism and so is the leading genetic cause of life-threatening obesity in children. Along with digestion, PWS can impact hormones, strength, behavior, cognition, temperature regulation, pain, and sleep. These kiddos need to be taught about healthy eating and staying active from a young age. The condition is very rare, affecting only 1 in 15,000 people, but if you happen to know someone with this condition, take time this month to invite them to a park or a walk around the neighborhood.