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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
HAYDEN
Diagnosis: Spina Bifida (SB)/Myelomeningocele, Arnold Chiari II, III & IV Brain Malformation
SOLANA
Diagnosis: Severe Combined Immunodeficiency (SCID)
SOLICE
Diagnosis: Lennox Gastout Syndrome, Trisomy 5, Cri-du-chat (several others as well)
NOLA
Diagnosis: PANS, CVI, JIA & Others
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