Each year, Opération Enfant Soleil honours the courage of one child from each of Quebec’s administrative regions. Follow each child’s journey through the fact sheets and videos that tell their story.
Click here to access the stories of Enfants Soleil from other region and previous years (French only).
To aplu for your child, fill out our online form. For any other information, contact Amélie Pagé by email at email@example.com or at 1 877 683-2325, ext. 164.
You or your child have benefited from equipment financed by Opération Enfant Soleil while visiting a major pediatric centre or a regional hospital in Quebec?
We would like to hear your journey!
Send us your story along with a few photos via firstname.lastname@example.org.
13 years old | In remission from acute lymphoblastic leukemia
11 years old | Diagnosed with bradycardia and suffering from an unknown disease attacking the immune system
14 years old | Diagnosed with severe congenital scoliosis
10 years old | Diagnosed with type 1 diabetes and attention deficit and in remission from polyarticular juvenile idiopathic arthritis with enthesitis
9 years old | Diagnosed with craniopharyngioma
4 years old | Diagnosed with bronchomalacia, laryngomalacia and persistence of ductus arteriosus
9 years old | Diagnosed with spastic hemiparesis, uncontrolled severe epilepsy not (Lennox-Gastaut syndrome), severe intellectual disability and visual impairment
4 years old | Diagnosed with juvenile arthritis
12 years old | Diagnosed with visual pathway glioma, hydrocephaly and a generalized anxiety disorder
3 years | Diagnosed with two heart defects (tricuspid atresia and ventricular septal defect)
11 years old | Diagnosed with glutaric aciduria type 1
3 years old | Diagnosed with Noonan syndrome
17 years old | Diagnosed with Crohn’s disease, polyarthritis, immune deficiency, adrenal gland failure and psoriasis
5 years old | Diagnosed with congenital arthrogryposis
11 years old | Diagnosed with type-2 spinal muscular atrophy, osteopenia and severe asthma
7 years old | Diagnosed with cerebral palsy, epilepsy, gastroparesis, severe dysphagia, a severe speech disorder, scoliosis and moderate to severe intellectual disability and partial blindess
2 years old | Diagnosed with 16p13.11 microdeletion syndrome
6 years old | Diagnosed with mucopolysaccharidosis type VI (Maroteaux-Lamy) and sleep apnea