Children under the age of 2 who are diagnosed as a rare disease-chubby Willie syndrome can be treated with the support of the Growing Angel Fund of the Red Cross Foundation. The subsidy standard is a one-time subsidy for each patient for half a year, and each patient can apply for subsidy twice at most.

Pride-Willi syndrome (PWS), commonly known as chubby Willie, is a complex disease caused by genetic material changes in specific chromosome regions. The etiology is a series of rare neurodevelopmental diseases with cognitive, behavioral, neurological and endocrine disorders caused by the gene defect of chromosome 15.

The main symptoms are: pale skin, early feeding difficulty, crying weakness, insufficient muscle tension, accompanied by special face, short stature, small hands and feet, growth retardation, mental retardation, gonadal dysplasia and serious behavior problems. At the same time, due to the dysfunction of hypothalamus, children generally begin to have irresistible hyperappetite and strong food-seeking behavior from about 2 years old, which leads to severe obesity, metabolic disorder, hypertension, coronary heart disease, sleep apnea and other complications, and even the danger of sudden death.