Prenatal Experiences and Desires With Early Intervention for Families of Children With Down Syndrome

被引:0
|
作者
Keilty, Bonnie [1 ,3 ]
Jackson, Melissa A. [1 ]
Smith, Janediane [2 ]
机构
[1] CUNY, Hunter Coll, New York, NY USA
[2] Univ North Carolina, Charlotte, NC USA
[3] CUNY, Hunter Coll, Dept Special Educ, 695 Pk Ave,916 West, New York, NY 10065 USA
关键词
prenatal intervention; early intervention; family capacity-building; Down syndrome; qualitative research; SERVICE COORDINATION; YOUNG-CHILDREN; HEALTH-CARE; DIAGNOSIS; PREGNANCY; OUTCOMES; PEDIATRICIAN; EDUCATION; FEELINGS; PARENTS;
D O I
10.1177/02711214241237420
中图分类号
G76 [特殊教育];
学科分类号
040109 ;
摘要
Part C early intervention (EI) starts no earlier than birth, even with a prenatal diagnosis resulting in automatic eligibility. Despite other early home visiting programs beginning prenatally and the increasing likelihood of uncovering certain diagnoses prenatally, pregnant families cannot access EI. This study sought to understand families' perspectives on their desire for prenatal EI and how EI could support them. Seventeen primarily White non-Hispanic mothers with a prenatal diagnosis of Down syndrome shared their prenatal experiences through retrospective, qualitative interviews. Three themes emerged: (1) prenatal period as a time to connect to EI, (2) different families, different prenatal desires, and (3) postnatal EI experiences, prenatal EI hopes. Families saw benefits to starting prenatally to enroll in and understand EI, and prepare for their baby's arrival through individualized outcomes. Families appreciated their postnatal EI and envisioned similar supports prenatally. Participants' shared experiences are discussed in relation to pre- and postnatal EI.
引用
收藏
页码:277 / 289
页数:13
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