Familjehemsvård är den vanligaste placeringsformen i Sverige för barn som inte kan bo med sin familj. När sammanbrott sker berörs de närmast involverade. Syftet var att genom en allmän litteraturöversikt undersöka familjehemsföräldrars perspektiv på sammanbrott i familjehemsvård. 10 vetenskapliga artiklar låg till grund för resultatet som analyserades med hjälp av sorg- och kristeori samt salutogenetiskt perspektiv. Resultatet visade att sammanbrott väcker olika känslor som sorg, förlust, lättnad och ångest. Familjehemsföräldrar kände sig misslyckade och upplevde sig ha svikit barnet. Dessa känslor kunde även leda till en identitetskris hos familjehemsföräldrarna. Vidare uppmärksammades att relationen till, och kommunikationen med, socialtjänsten påverkade upplevelsen av sammanbrott. Brister i samverkan med socialtjänsten kunde negativt påverka stödet till familjehemsföräldrarna. / In Sweden, family foster care is the most common form of placement for children who cannot live with their families. Disruptions in placements can occur and affect those most immediately involved. The purpose of this literature review was to explore foster parents’ perspectives on placement breakdown. The result was based on 10 scientific articles that were analyzed through bereavement theory and salutogenic perspective. Results show that placement disruption awakens emotions such as sorrow, loss, relief and anxiety. Foster parents’ experienced failure and felt that they had betrayed the child. These feelings could also lead to an identity crisis for the foster parents. Further observations indicated that the relationship to, and communication with, social services affected foster parents’ perceptions of disruption. The shortcomings in collaboration with social services could influence the support offered to foster parents in a negative way.

Thesis (M Social WOrk (Social Work)--University of Stellenbosch, 2007. / This research provides an overview of foster care and investigates the support and training of foster parents as well as the issues foster parents need to manage on a regular basis. The basic premise for this research is the importance of social workers becoming aware of the issues foster parents manage on a regular basis as well as the support and training needs of foster parents. It is important for foster parents to receive support as well as social workers and family care organisations to develop and implement appropriate training programmes for foster parents on an ongoing basis. Fostering affects and requires the involvement of the entire foster family as well as relevant role players and professionals. It is therefore necessary to consider the foster parents and foster family as part of the larger fostering arena, and not to be supported and trained in isolation. The nature of the foster placement will inevitably influence the development of the foster child, meeting the needs of the foster child as well as the effect that the placement has on the foster family. The purpose of this research is to broaden the theoretical knowledge of professionals working with foster parents, and specifically social workers and family care organisations, in identifying foster parent’s training and support needs. This research report includes an investigation of the issues foster parents and foster families manage on a regular basis as well as the nature of and benefits of support and training for foster parents. Knowledge of these issues foster parents manage while fostering will increase the awareness and the ability of the social worker or other professionals to provide training and support to the relevant foster parents.

In my thesis I deal with temporary foster care where the aim of the thesis is to analyse the process of child's introduction and transition into the care of future adoptive parents and to map out the experience and opinions of both future adoptive and temporary foster parents. The partial objective is to identify the opportunities and risks of this process, focusing on the subjective experience of the research participants. In order to reach the set target a method of qualitative research was chosen, namely an interview, specifically the technique of an unstructured interview. The research was divided into two parts. In the first part of the research interviews were conducted with future adoptive parents and in the second part with temporary foster parents who had at least two children in their care. For evaluation of results a cluster analysis was used. The results of the research show that future adoptive parents have considerable reservations about the process of getting acquainted with the child; their experience regarding the actual transition of the child into their care vary. Moreover they perceive the impact of this process on the child rather negatively. Further, the research shows that most temporary foster parents do not have a negative experience with introduction and transition of the child into the care of future adoptive parents. However, the whole research has revealed many pitfalls in this process. Intended merit of this thesis lies in the fact that the results can be used as a source of information for social workers, prospective adoptive parents, temporary foster parents and for staff of support organizations or general public.

This research project surveyed San Bernardino County non-relative licensed foster parents to assess their level of satisfaction with the Department of Children's Services. This research also explored factors related to communication and feelings of support and determined their impact on over all feelings of satisfaction with the agency.

Indiana University-Purdue University Indianapolis (IUPUI) / Awaiting adoption is a social problem in America that affects thousands of children as well as families, agencies, communities, the mission of the child welfare system, and society at large. In 2014, over 101,000 children were awaiting adoption in the United States. On average, waiting children have been in out-of-home care for approximately three years. One phenomenon that plagues waiting children and their opportunity for adoption is the disruption of their pre-adoptive placements or the change in a waiting child's placement prior to a finalized adoption. Despite unique placement and permanency needs, waiting children and their foster parents are seldom recognized as unique cohorts. Thus, little is known about the experience of pre-adoptive placement disruption. The status of waiting children, foster care and adoption history and policy, and literature and theory relevant to pre-adoptive placement disruption are discussed. In-depth, semi-structured interviews and Interpretive Phenomenological Analysis were used to investigate the research question: What is the experience of pre-adoptive placement disruption for pre-adoptive foster parents? Eleven foster parents participated in nine interviews. Participants were licensed through public or private child welfare agencies. The majority of participants were married, Caucasian, and had adopted from foster care. Important findings emerged from the experiences participants shared. Pre-adoptive placement disruption is characterized by "compound loss" including both the loss of the child and the loss of purpose. Participants experienced the disruption like a broken social contract and attributed the disruption to the child welfare system or the children's perpetrators. Disruption experiences resulted in lasting effects including changes to the profiles of the children participants would foster or adopt in the future, pre-adoptive status, and advocacy efforts. Resolve emerged as a critical factor for participants to approach foster and pre-adoptive care in new ways. Vulnerability, isolation, and ambivalence emerged as essential elements of living through disruption. Findings suggest the importance of assessing pre-adoptive parents' motivations and expectations, validating their experiences, acknowledging their losses, and practicing with transparency and competency. Implications exist for child welfare and social work practice and education. Additional research is needed regarding barriers and supports of adoption from foster care.

This paper aims to describe the social workers relationship / contact to the foster parents' own children in a foster home. The aim is also to understand a social workers perspective on foster parents' own children in the foster home. We wanted to find out how social workers relationship/contact to the foster parents own children looks like, which has shown to differ between municipality to municipality. The study has shown that the perspective on the own children in the family, differs from municipality to municipality and that the own children’s meaning for the foster home as a social contribution, has a varied meaning amongst social workers. Based on several theories and concepts we have analyzed our result we got from the interviews, we found out that social workers looks at and works differently with foster parents own children. We found out that social workers perspective on foster parent’s own children is, that they are a very important resource and they participate in the fostering of the foster child. It also became clear in our result that a paradox appears in social workers work when although they don’t have any regulated documents on how to work with the foster parent’s own children, they still experience that they are restricted in their work by the organization they work under.

Syftet med denna studie var att undersöka upplevelsen av stödet som ges till familjehem via en konsulentstödd verksamhet. Frågorna för studien var hur familjehemsföräldrarna och personalen upplever stödet. Tre familjehemskonsulenter och två familjehemsföräldrar intervjuades. Med en kvalitativ metod och en fenomenologisk inriktning kunde upplevelsen av konsulentstödet studeras. För att få en förståelse för intervjumaterialet användes två olika analys perspektiv i form av systemteorin och utvecklingsekologin. Resultatet visade i likhet med tidigare forskning att viktiga delar i stödet var tillgänglighet, information, relationer, utbildning, handledning och träffar med andra familjehem. Resultatet visade att båda familjehemsföräldrarna i studien var nöjda med konsulentstödet överlag. I studien framkom dock att verksamheten inte kunde erbjuda nya familjehem utbildning innan en första placering görs vilket familjehemsföräldrarna framhävde som väsentligt. Verksamheten hade även sämre möjligheter att erbjuda en bra kontinuerlig utbildning i form av föreläsningar. Studiens resultat tillsammans med tidigare forskning visade även att upplevelsen av ett bristande nätverk finns hos familjehemsföräldrar. / The purpose of this study was to investigate the experience of the support given to the family home through a consultant supported activities. The questions for the study was how the foster parents and staff feel the support. Three family advisers and two foster parents were interviewed. With a qualitative method and a phenomenological focus could be the experience of consultant support are studied. To get an understanding of the interviews, two different analytical perspectives in the form of systems theory and the development of ecology. The results showed, as in previous research that the key elements in supporting the accessibility, information, relationships, training, tutorial and meet with other foster homes. The results showed that both the foster parents in the study were satisfied with consultant support overall. The study showed, however, that the business could offer new foster training before an initial investment made which foster parents mattered significantly. Operations were also less able to offer a good continuous education in the form of lectures. The study's results together with previous research also showed that the perception of a lack of available network of foster parents.

Thesis (M Social Work)--Stellenbosch University, 2015. / ENGLISH ABSTRACT: Non-biological caregivers often take children into their care when their own biological caregivers have failed to provide them with a safe and loving home. These children are often also affected with Fetal Alcohol Spectrum Disorders (FASD). Learning of a child’s disability can be a big shock to non-biological caregivers especially if it is misunderstood, available professional help is scarce and intervention resources are not readily available. These non-biological caregivers are often not prepared for the financial, emotional and physical investment that is required to fully support the children and their development. This can cause various emotional reactions and implications that are challenging for the caregivers. It is critical to recognise parenting experiences and challenges as a means of developing and promoting intervention strategies and support that will respond to the needs of the children with FASD and their non-biological caregivers especially from a South African perspective. There is a need for social workers to take on responsibility for addressing FASD as they have the professional capacity to help families living with FASD to develop and maintain stable and nurturing households. One way in which this can be achieved is through the initiation and facilitation of support groups. The goal of the study was to gain an understanding on the experiences of non-biological caregivers of children with FASD and of the utilisation of support groups to help them cope better. The researcher made use of a combination of an exploratory and descriptive research design. By using both a quantitative and qualitative approach in a complimentary manner, the researcher was able to gain an in depth insight into the lives of the non-biological caregivers and how they experience this disability and support groups that are utilised as a means of helping them cope. Permission to conduct the study was granted by the committee for Human Research at the University of Stellenbosch. The literature study firstly investigated the implication of FASD on affected children. Secondly, the extents to which non-biological caregivers are affected by the consequences of this disability were discussed. After this the utilisation of support groups as a method of supporting non-biological caregivers, with the emphasis on a mutual-aid and educational approach as theoretical underpinning was described. The empirical study was completed with 16 participants through face-to-face, semi-structured interviews. An interview schedule based on the findings of the literature study was utilised. The criteria for inclusion were that participants had to have attended at least 5 support group sessions and had to be a non-biological caregiver of FASD children who had attended the support groups specifically related to this disorder. The results of this study mostly confirmed the findings from the literature study which showed that support groups play a vital role in providing necessary support to non-biological caregivers who are often unprepared for the realities of caring for a FASD child. Recommendations are aimed at the social work profession in South Africa who need to align itself in providing necessary support to non-biological caregivers through the use of support groups and various other methods of service rendering. Suggestions for future research are also made in line with how non-biological caregivers can be supported in their unique caregiver responsibilities. / AFRIKAANSE OPSOMMING: Nie-biologiese versorgers neem dikwels kinders in hul sorg wanneer kinders se biologiese ouers versuim om vir hulle ‘n veilige en liefdevolle huis en omgewing te skep. Hierdie kinders kan ook ly aan of geaffekteer word deur Fetale Alkohol Spektrum Versteuring (FASV). Dit kan ‘n groot skok wees wanneer versorgers uitvind dat die kind geaffekteer is daardeur, veral as hierdie versteuring misverstaan word. Professionele hulp is skaars, en intervensies en hulpbronne is nie vryelik beskikbaar nie. Versorgers is dikwels nie voorbereid op die finansiële, emosionele en fisiese eise wat nodig is om ten volle die kind se ontwikkeling te ondersteun nie. Dit kan dit lei tot verskillende emosionele reaksies met verskeie gevolge wat opsigself ook verskeie uitdagings vir die nie- biologiese versorgers veroorsaak. Dit is van kritieke belang om die ervarings en uitdagings van ouerskap te verken in die bevordering en ontwikkeling van intervensiestrategieë ter ondersteuning van die behoeftes van die kinders met FASV en hul versorgers, veral vanuit ‘n Suid-Afrikaanse perspektief. Daar word vereis van maatskaplike werkers om verantwoordelikheid te neem vir die aanspreek van FASV, aangesien hulle die professionele kapasiteit het om families wat geaffekteer is te help, en om hulle by te staan sodat ‘n stabiele en koesterende huishouding ontwikkel en volgehou kan word. Een manier waarop dit bereik kan word, is deur die vestiging en fasilitering van ondersteuningsgroepe. Die doel van hierdie studie was om ‘n begrip te ontwikkel oor die ervarings van nie-biologiese versorgers van kinders met FASV se benutting van ondersteuningsgroepe. Die navorser het gebruik gemaak van ‘n kombinasie van ‘n verkennende en beskrywende navorsing. Deur die gebruik van beide ʼn kwantitatiewe en kwalitatiewe benadering, is die navorser in staat gestel om ‘n indiepte insig in die lewens van die versorgers te bekom, en ondersoek in te stel oor hul ervarings van die versteuring/gestremdheid deur ondersteuningsgroepe wat as intervensie aangewend is. Toestemming om die studie te doen is deur die Etiese Komitee vir Menslike Navorsing aan die Universiteit van Stellenbosch bekom. Eerstens is die literatuurstudie voltooi waarin die navorser ondersoek ingestel het oor die implikasies van FASV op geaffekteerde kinders. Tweedens is daar bespreek hoe nie-biologiese versorgers geraak word deur die gevolge van hierdie versteuring/gestremdheid. Daarna is ondersteuningsgroepe as ‘n metode van ondersteuning aan versorgers ondersoek, en klem is gelê op ‘n wedersydse hulpbenadering en ‘n opvoedkundige benadering as teoretiese grondslag. Die empiriese studie is voltooi met 16 deelnemers deur middel van individuele, een-tot-een, semi-gestruktureerde onderhoude. ‘n Onderhoudskedule, wat gebaseer is op die bevindinge van die literatuurstudie, is gebruik. Die kriteria vir deelname aan die studie en groep het ingesluit dat deelnemers ten minste vyf sessies van ‘n ondersteuningsgroep moes bywoon en ook ‘n pleegouer wees van ‘n FASV kind. Die resultate van hierdie studie het meestal die bevindinge uit die literatuurstudie bevestig en het getoon dat ondersteuningsgroepe ‘n belangrike rol speel in ondersteuning aan nie-biologiese versorgers, wat dikwels onvoorbereid is op die werklike problematiek van die versorging van ‘n kind met FASV. Aanbevelings word gerig aan die maatskaplikewerk-professie in Suid-Afrika, ten einde ondersteuningsgroepe en ander metodes van dienslewering te bied, ter ondersteuning aan die versorgers van FASV kinders. Voorstelle vir verdere navorsing word ook gemaak sodat daar ‘n ondersteuningsnetwerk opgebou kan word vir die versorgers van ‘n FASV kind ten einde aan hulle unieke versorgingsbehoeftes te voorsien.

published_or_final_version / Social Work / Master / Master of Social Work

The aim of this study was to gain a better understanding of possible foster families’ views on fostering a child and what they consider to be important factors for deciding whether or not to become a foster family. The studys result is based on five semi-structured interviews with persons whom have an interest for becoming foster families and the findings were analyzed by using a norm theory. The way that the interviewed people described their views on fostering a child could in the analysis be seen as a result of different norms and they often described the ideal foster family based on either their own family or the nuclear family.