Types of Disabilities Served
A high percentage of PASCO’s clients have both physical and developmental disabilities particularly, Cerebral Palsy. Many of the adults have spinal cord injuries and Multiple Sclerosis.
PASCO provides high quality care for dozens of disabilities, including:
- Autism
- Multiple Sclerosis
- Cerebral Palsy
- Alzheimer’s
- Down Syndrome
- Muscular Dystrophy
- Spina Bifida
- Quadriplegia
- Traumatic Brain Injuries
- Spinal Cord Injuries
- Intellectual Disabilities
- Child and Pediatric Disabilities
- Parkinsons
Additional Disabilities Served:
22Q11 Deficiency, Acrocephalosyndactyly, Alcohol Liver Damage, Angelmans, Syndrome, Anoxia, Anoxic Brain Damage, AOA-APRAXIA Occulatmotor Ataxia, Aquired Hypoventilation, Arthritis, Arthrogreyposis, Arthrogryposis, Asthma, Autistic, Autosomal Anomalies, Autosomal, Deletions, Blindness, Brain Anomaly, Brain Deformity, Brain Stem Confusion, Broncho Pulmonary Dysplasia, Bullous Dermatoses, Cerebral Aneurysm, Cerebral Degeneration, Chromosome 18P Disorder, Chromosome Anomaly, Chromosome Translocation, Chronic Lung Disease, Chronic Respiratory Disorder, Cleft Palate & Lip, Congenital Abnormalities, Congenital Heart Disease, Congenital Hydrocephalus, Congenital Quadriplegia, Constipation, Convulsions, COPD, Deficiency of Cell Mediated Immunity, Dementia, Development Delay, Diabetes, Diencephalic Syndrome, Dis Mitochondrial Metabolism, Down’s Syndrome, Dravert Syndrome, Dwarfism, Dysphagia, Encephalitis, Encephalocele, Encephalopathy, Epidermolysis Bullosa, Epilepsy, Esophageal Reflux, Extrapyramidal Disorder, Facial Bone Anomaly, Fetal Alcohol Syndrom (FAS), FG Syndrome, Fragile X Syndrome, Friedreich’s Ataxia, Genetic Deletion 4P, Genetic Disorder, Goldenhar Syndrome, Head Injury, Hemiplegia, Hemiplesia, Holoprosencephaly, Hydrocephalus, Hypertension, Idiopathic Encephalopathy, Intestinal Malabsorption, Inverted Duplicated 8P Trisomy, Kabuki Syndrome, Klinefelter’s Syndrome, Krabbe’s Disease, Lennox Gastaut Syndrome, Leukemia, Leukodystrophy, Leukomalacia, Lipidoses, Lissencephaly, Malignant Brain Tumor, Mental Retardation, Metabolism Disorder, Microcephalous, Mid Brain Defect, Mild Mental Retardation, Mitochandrial Myopathy, Mitochondrial Disorder, Mixed Development Disorder, Mucopolysaccharidosis, Multiple Sclerosis, Muscle Weakness – General, Muscular Dystrophy, Myoclonus, Myopathy, Myotonic Disorders, Neurofibromatosis, Neuropathy In Diabetes, Open Lip Schizencephaly, Opitz Syndrome, Optic Nerve Disorder, Osteoporosis, Paralytic Syndrome, Paraplegia, Parkinsons, Patau’s Syndrome, Perinatal Condition, Pervasive Development Disorder, Phenylketonuria, Prader-Willi Syndrome, Profound Mental Retardation, Psychomotor Retardation, Pulmonary Circulatory Disorder, Quadriplegia, Respiratory Disease, Retts Syndrome, Ring Chromosome #22, Russell Silver Syndrome, Schizencephaly, Seizure Disorder, Seondary Parkinsonism, Severe Mental Retardation, Shaken Infant Syndrome, Sjogren Larson Syndrome, Spina Bifida, Spinal Muscular Atrophy, Steven Johnson’s Syndrome, Stroke, Tramatic Brain Injury, Trisomy 18 – Edwards’ Syndrome, Trisomy 4P+, Trisomy 8, Tuberous Sclerosis, Wolf Hirschhorn Syndrome, X-linked FG Syndrome and undiagnosed.
