Some of the conditions we support are listed below
A
- Achondroplasia
- Acquired Brain Injury
- ADHD
- Adrenal Insufficiency
- Agenesis of the Corpus Callosum
- Aicardi Syndrome
- Alopecia
- Amputation
- Andermann Syndrome
- Angelman Syndrome
- Antithrombin 3 Deficiency
- Arthrogryposis
- Arts Syndrome
- Asperger Syndrome
- Ataxia
- Ataxia Telangiectasia
- Auditory Processing Disorder
- Autism Spectrum Disorder
- Axonal Neuropathy
B
- Batten Disease
- Batten Disease
- Benign Joint Hypermobility Syndrome
- Benign Joint Hypermobility Syndrome
- Brain Injury
- Brain Injury
- Bulbar Palsy
- Bulbar Palsy
C
- Cardiac Difficulties
- Cardiac Difficulties
- Cardiofaciocutaneous Syndrome
- Cardiofaciocutaneous Syndrome
- Central Auditory Processing Disorder
- Central Auditory Processing Disorder
- Cerebral Palsy
- Cerebral Palsy
- Charcot Marie Tooth Disease
- Charcot Marie Tooth Disease
- CHARGE Syndrome
- CHARGE Syndrome
- Chiari Malformation
- Chromosomal Disorder
- Chronic Lung Disease
- Cleft Palate
- Cognitive Impairment
- Congenital Glaucoma
- Congenital Higher Airway Obstruction Syndrome (CHAOS)
- Congential Heart Disease
- Cortical Vision Impairment
- Creatine Transporter Deficiency
- Cri-Du-Chat Syndrome
- Crohn’s Disease
- Cystic Fibrosis
- Cytomegalovirus
D
- Dandy-Walker Syndrome
- Development Delay
- DiGeorge Syndrome
- Down Syndrome
- Dravet Syndrome
- Duchenne Muscular Dystrophy
- Dumping Syndrome
- Dysarthria
- Dyslexia
- Dysphasia
- Dyspraxia
- Dystonia
E
- Ectodermal Dysplasia
- Ehlers-Danlos Syndrome
- Epidermolysis Bullosa
- Epilepsy
- Erb’s Palsy
F
- Facioscapulohumeral Dystrophy
- Foetal Alcohol Syndrome
- Fragile X Syndrome
G
- Geliophysic Dysplasia
- Goldenhar Syndrome
H
- Hearing Impairment
- Heart Condition
- Hemiplegia
- Hereditary Coproporphyria
- Hip Dysplasia
- Hydrocephaly
- Hypermobility Joint Syndrome
- Hypochondroplasia
- Hypopituitarism
- Hypotonia
- Hypoxic Ischemic Encephalopathy
I
- Intellectual Disability
- Irlen Syndrome
J
- Joubert Syndrome
- Juvenile Idiopathic Arthritis
K
- Keratoconus
- Klinefelters Syndrome
L
- Learning Difficulties
- Lissencephaly
M
- Macrocephaly
- Melas Syndrome
- Merosin Deficiency Myopathy
- Merosin Deficient Muscular Dystrophy
- Metachromatic Leukodystrophy
- Metatarsus Adductus
- Microcephaly
- Migrating Partial Epilepsy in Infancy
- Miller-Dieker Syndrome
- Mitochondrial Disease
- Moebius Syndrome
- Molybdenum Cofactor Deficiency
- Mowat-Wilson Syndrome
- Moyamoya Disease
- Mucolipidosis
- Muscular Atrophy
- Muscular Dystrophy
- Myofibrillar Myopathy
- Myotonic Dystrophy
N
- Nemaline Myopathy
- Nephrotic Syndrome
- Nerve Palsy
- Neuronal Migration Disorder
- Neuropathy
- Nystagmus
O
- Ohdo Syndrome
- Oppositional Defiance Disorder
P
- Periventricular Leukomalacia
- Phelan-McDermid Syndrome
- Pierpoint Syndrome
- Pierre Robin Syndrome
- Pitt-Hopkins Syndrome
- Plagiocephaly
- Polymicrogyria
- Pseudohypoaldosteronism
R
- Reactive Attachment Disorder
- Receptive Language Disorder
- Respiratory Distress Syndrome
- Retinoblastoma
- Retinopathy
- Rett Syndrome
- Rubinstein-Taybi Syndrome
S
- San Filipo Syndrome
- Scoliosis
- Seizure Disorder
- Sensory Polyneuropathy
- Sensory Processing Disorder
- Separation Anxiety Disorder
- Sleep Apnoea
- Sotos Syndrome
- Speech Impairment
- Spina Bifida
- Spinal Cord Injury
- Spinal Muscular Atrophy
- Spondyloephiphyseal Dysplasia Congenita
- Stroke
- Surfactant Protein-C Deficiency
T
- Talipes Equinovarus
- Thalessemia
- Tourette Syndrome
- Trichotillomania
- Trisomy 13
- Turner Syndrome
U
- Ullrich Congenital Muscular Dystrophy
- Undiagnosed Conditions
V
- VACTERL Association
- Vision Impairment
W
- Williams Syndrome
- Wolf Hirschhorn Syndrome
X
- Xeroderma Pigmentosum