Our Dream Journals

Click on a child's name to read milestone updates from our CC4C Children!

Isabella 

Diagnosis: PCDH19 Epilepsy
 

Sophia 

Diagnoses: Chiari Malformation,

Chromosome Duplication 1Q21.1
 

Nicolette

Diagnosis: Chromosome Deletion

10q22.3q23.2
 

Charlotte 

Diagnosis: PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infection)
 

Mila 

Diagnosis: Microcephaly Lymphedema Chorioretinal Dysplasia
 

Mia 

Diagnoses: Systemic Juvenile Rheumatoid Arthritis (JRA), Inflammation of the Liver and Lymph Nodes
 

Lily

Diagnoses: ADNP Syndrome, Epilepsy,

Malignant Hypothermia
 

Kyle 

Diagnosis: ADNP Syndrome
 

Tyler

Diagnosis: Rare Genetic Brain Malformation
 

Emalyn

Diagnosis: Infantile Scoliosis
 

Ava 

Diagnosis: Mitochondrial Depletion Syndrome
 

Irene

Diagnosis: Williams Syndrome
 

Cooper 

Diagnosis: Beckwith Wiedemann Syndrome
 

Avery 

Diagnosis: Monogenic Autoinflammatory Disorder and Hypermobile Ehlers Danlos
 

Ty

Diagnosis: Primary Hyperoxaluria