Nurse-Family Partnership United Way of the Coastal Bend provides home visiting services and promotes health and human services to ensure that all children are healthy. The program is available for first time mothers-to-be. They are voluntary services that match parents with trained professionals to provide information and support during pregnancy and throughout their child’s first five years. The mother needs to sign up for the program before the 28th week of pregnancy. All services are provided FREE of charge.Some of the programs offered are Early Head Start, Home Instruction for Parents of Preschool Youngsters (HIPPY), and Parents as Teachers. These programs are for pregnant women and parents of all children birth to age five. Application can be found on the website.
4659 Everhart
Corpus Christi, 78411, TX
Building Name or Description: Nueces County Community Action Agency
Accessible Location: Yes
Type of Organization | Nonprofit (501c3) |
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Categories | Emotional Support, Health & Fitness, Social Media, Training, Volunteer Opportunity |
Services offered in Spanish? | yes |
Newsletter? | yes |
Child Care Available? | No |
Age Range | Birth - 3 , 3-5 |
Disability Categories | Developmental Disability, Genetic or Congenital Disorder, Intellectual Disability, Learning Disability, Medical Condition, 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? | No |
Website | https://www.uwcb.org/nfp |
Contact Name | Laura Drummond |
Email Address | [email protected] |
Phone Number | 361-882-2529 |