Five years ago little Léa was born. Since birth, Amandine and Yoann, her parents and their families and friends, have accompanied her in her daily struggle at home and in the hospital. A fight once morest cystic fibrosis, a rare and incurable disease. Today, Léa continues her schooling in kindergarten accompanied by her AESH (accompanying student with disabilities). “Especially since this year she was able to benefit from a new treatment, confides her mother, which allowed her to go to school more often and more comfortably with her friends. To practice some activities such as classical dance at the conservatory, gymnastics or outings.” A fairly normal life for a girl of her age, whose mother has finally obtained the
