eParent.com is an online multi-media company dedicated to be the ultimate resource for everything related to the special needs community. Providing practical advice, emotional support, current trending news and educational information to empower caregivers and families of children and adults with disabilities and special healthcare needs. As well as to the physicians, allied health care professionals, and educational professionals who are involved in their care and development.
eParent uses a multi-media approach to disseminate information and connect to a diverse and passionate special needs community of families, caregivers, professionals and organizations through...
350 South Grand Avenue
Los Angeles, 90071, CA
Accessible Location: No
|Type of Organization||For Profit|
|Categories||Advocacy, Emotional Support, Resource/Lending Library, Special Education, Other|
|Services offered in Spanish?||No|
|Child Care Available?||No|
|Age Range||All Ages , Birth - 3 , 3-5 , 6-11 , 12-14 , 15-21 , 22 and up|
|Disability Categories||Developmental Disability, Genetic or Congenital Disorder, Intellectual Disability, Learning Disability, Medical Condition, Mental Health Disorder, Physical Disability|
|Does this organization belong to all disabilities?||yes|
|This organization belongs to these diagnoses||22q11.2 Deletion Syndrome, 3-methylcrotonyl-CoA Carboxylase Deficiency, Achondroplasia (Dwarfism), Alpha Thalassemia, Anencephaly, Angelman’s Syndrome, Anorexia Nervosa, Antiphospholipid Syndrome (aPL), Anxiety Disorders, Aortic Stenosis, Arrhythmia, Asthma, Atopic Dermatitis, Atrial Septal Defect (ASD), Attention Deficit Hyperactivity Disorder (ADHD), Autism Spectrum Disorder (Pervasive Developmental Disorder), Autoimmune Diseases, Beta Thalassemia, Biliary Atresia, Bipolar Disorder, Bone Cancer, Brain Cancer, Brown’s Syndrome, Bulimia Nervosa, Cancer Treatment for Children, Cardiomyopathy, Celiac Disease, Cerebral Palsy, Chiari Malformations, Chromosomal Anomalies - Trisomy 13 (Patau’s, D1) & Trisomy 18 (Edward’s, E3), Chronic Lung Disease (CLD), Bronchopulmonary Dysplasia (BPD), Cleft Lip and Palate, Clubfoot, Conduct Disorder, Congenital Heart Disease, Congestive Heart Failure, Craniofacial Anomalies, Craniosynostosis, Crohn’s Disease, Cystic Fibrosis, Deafness, Depression, Diabetes (Type 1), Diabetes (Type 2), Diaphragmatic Hernia, Diarrhea, DiGeorge Syndrome, Down Syndrome - Trisomy 21, Duchenne Muscular Dystrophy, Eating Disorders, Eczema (Atopic Dermatitis), Epilepsy, Epispadias, Ewing Sarcoma (Bone Cancer), Exstrophy of the Bladder and Epispadias, Failure to Thrive, Fetal Alcohol Spectrum Disorder (FASD), Fetal Alcohol Syndrome (FAS), Fibromyalgia, Fragile X Syndrome, Gastroesophageal Reflux (GER), Genetic Disorders, Glomerulonephritis, Goldenhar’s Syndrome (Oculoauriculovertebral Dysplasia), Hearing Loss (Deafness), Heart Failure, Heart Murmurs, Heart Transplant, Hemiplegia (Paralysis), Hemoglobin C Disease, Hemoglobinopathies, Hemophilia, Hepatitis in Children, Hirschsprung’s Disease, HIV/AIDS, Hodgkin Lymphoma, Homocystinuria, Hydrocephalus, Hypospadias, Hypothyrodism in Children, Immune Thrombocytopenic Purpura (ITP), Inflammatory Bowel Disease (IBD), Intestinal Malrotation and Volvulus, Intraventricular Hemorrhage (IVH), Iritis, Juvenile Dermatomyositis, Juvenile Idiopathic Athritis (JIA), Juvenile Rheumatoid Arthritis (JRA), Juvenile Scleroderma, Kawasaki Disease, Kidney Failure, Leukemia, Lupus, Maple Syrup Urine Disease, Marfan Syndrome, Medium-chain acyl-CoA dehydrogenase Deficiency, Metabolic Syndrome, Microcephaly, Muscular Dystrophy, Myasthenia Gravis, Neuroblastoma, Neurofibromatosis, Neurotube Defects, Newborn Screening Tests, Non-Hodgkins Lymphoma, Obesity, Obsessive-Compulsive Disorder, Oppositional Defiant Disorder (ODD), Osteogenesis Imperfecta, Osteosarcoma (Bone Cancer), Patent Ductus Arteriosus (PDA), Periventricular Leukomalacia (PVL), Pervasive Developmental Disorder, Phenylketonuria (PKU), Post-Traumatic Stress Disorder (PTSD), Prader-Willi Syndrome, Prematurity, Prune Belly Syndrome, Quadriplegia (Paralysis), Renal Failure (Kidney Failure), Retinoblastoma, Rheumatic Heart Disease, Schizophrenia, Scoliosis, Seizures and Epilepsy, Severe Combined Immunodeficiency (SCID), Sickle Cell Disease, Spina Bifida, Systemic Lupus Erythematosis (Lupus), Tetralogy of Fallot, Torticollis (Congenital Muscular Torticollis), Tourette Disorder, Tuberous Sclerosis, Turner Syndrome, Ulcerative Colitis, Velocardiofacial Syndrome, 22q11.2 Deletion Syndrome, DiGeorge Syndrome, Ventricular Septal Defect (VSD), Von Willebrand Disease, West Nile Virus, Wilms Tumor (Beckwith-Wiedemann Syndrome), Zika|
|Is this a statewide service?||yes|
|Contact Name||Jenna Turcich|
|Email Address||[email protected]|