Death of a Child to Tay-Sachs and other progressive neurological disorders: Long-term impact on parents’ emotional and personal lives

DSpace Repository

Show simple item record

dc.contributor.advisor Tsipis, Judith en_US
dc.contributor.author Williams, Elizabeth
dc.date.accessioned 2014-05-19T19:25:37Z
dc.date.available 2014-05-19T19:25:37Z
dc.date.issued 2014
dc.identifier.uri http://hdl.handle.net/10192/27096
dc.description.abstract Caring for and surviving the death of a child with a life-limiting illness has a profound and lasting effect on parents’ lives. Many studies have explored the emotional changes parents may experience shortly after their loss, but few have examined the long-term effects. It is important for genetic counselors that may work with these families to understand the range of experiences that can come with time. To explore the long-term experience, we designed an online anonymous survey that included questions about the deceased child’s illness and death, validated assessments of prolonged grief and posttraumatic growth, as well as questions about relationships with family, friends, work, and faith. We requested the participation of parents whose children died two or more years ago to a life-limiting, progressive, neurological condition through the National Tay-Sachs & Allied Diseases Association (NTSAD) and the National Mucopolysaccharidoses Society (MPS Society). Our study population, on average, experienced a moderate amount of posttraumatic growth, with a mean score of 27.62 on a 0-50 scale with highest scores in the subfactors of “appreciation of life” and “personal strength”. Some parents in our study reported difficulty motivating themselves for certain activities and trouble connecting with people who had not experienced a similar loss, but only a small minority of the study population met criteria for prolonged grief disorder (PGD). Since the death of their affected child, parents widely reported improvement in their relationships with their other children but little change in their relationships with parents, siblings, friends, colleagues and their work. Relationships with their partner or child’s other parent, as well as their personal faith and faith community experienced larger proportions of change, resulting in an almost even split between better, worse, and neither. Almost all of our 62 participants reflected on the care of their affected child without regret. The results of this study highlight the coexistence of difficulty and positive change in bereaved parents as well as the importance of support both during and after their child’s illness and death. en_US
dc.description.sponsorship Brandeis University, Graduate School of Arts and Sciences en_US
dc.format.mimetype application/pdf en_US
dc.language English en_US
dc.language.iso eng en_US
dc.publisher Brandeis University en_US
dc.relation.ispartofseries Brandeis University Theses and Dissertations
dc.rights Copyright by Elizabeth Williams 2014 en_US
dc.subject parental bereavement en_US
dc.subject posttraumatic growth en_US
dc.subject grief en_US
dc.subject life-limiting illness en_US
dc.subject Tay-Sachs Disease en_US
dc.subject meaning-making en_US
dc.title Death of a Child to Tay-Sachs and other progressive neurological disorders: Long-term impact on parents’ emotional and personal lives en_US
dc.type Thesis en_US
dc.contributor.department Graduate Program in Genetic Counseling en_US
dc.degree.name MS en_US
dc.degree.level Masters en_US
dc.degree.discipline Genetic Counseling en_US
dc.degree.grantor Brandeis University, Graduate School of Arts and Sciences en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search BIR


Browse

My Account