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 firstname.lastname@example.org 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 email@example.com.
2 years old | Suffering from severe Ebstein anomaly and atrial connection defect
6 months | Extremely premature
10, 9 and 3 years old | Premature
16 years old | Suffering from mucopolysaccharidosis type VI
5 years old | Extremely premature and suffering from severe bronchodysplasia
4 years old | Suffering from a still unknown genetic disease presenting multiple disabilities
7 years old | Suffering from polyuric renal failure
1 year old | Suffering from chronic septic granulomatosis
7 years old | Suffering from Wolf-Hirschhorn syndrome
16, 12 and 8 years old | Suffering from glutaric aciduria type 1
5 years old | Suffering from complex congenital cardiopathy and various disorders
11 years old | Suffers from refractory epilepsy caused by a brain tumour
3 and 2 years old | Suffering from a duplication of the ARID1B chromosome caused by Coffin-Siris syndrome
13 years old | Suffering from immune deficiency, asthma, severe vision problems, severe sleep apnea, verbal dyspraxia, a developmental coordination disorder, an attention disorder and cardiac arrhythmia.
3 years old | Suffering from tuberous sclerosis complex
1 year old | Suffering from several cardiovascular malformations
7 years old | Suffering from esophageal atresia, a laryngeal cleft, tracheomalacia, and bronchomalacia