Upbring is raising the standards for what childhood should be.
The harsh realities of child abuse and neglect often extend beyond the four walls of a home and into the fiber of our communities—in many cases stemming from a cycle of crime, economic disparity, mental health disorders and substance abuse. Every case of child abuse is different from the next because every child is unique, and so are their needs.
That’s why in order to break the generational cycle of child abuse, Upbring meets children and families in need right where they are. They then surround them with the services they need right then based on five key markers of every child’s success: safety, life skills, education, health and vocation. We call this our continuum of care.
8305 Cross Park Dr.
Austin, 78754, TX
Accessible Location: Yes
|Type of Organization||Nonprofit (501c3)|
|Categories||Counseling, Emotional Support, Financial, Trainings, Other|
|Spanish Services Offered?||No|
|Child Care Available?||No|
|Age Range||All ages|
|Disability Categories||Developmental Disability, Genetic Disorder, Intellectual Disability, Learning Disability, Medical Condition, Mental Health Disorder, Physical Disability|
|This organization pertains to all disabilities?||No|
|This organization pertains to these specific 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|