Young Adult Daughters of Lesbian Mothers Speak: A Qualitative Study on Identity Formation

2015 ◽  
Vol 11 (5) ◽  
pp. 465-492 ◽  
Author(s):  
Alicia K. Padovano-Janik ◽  
Virginia M. Brabender ◽  
Philip A. Rutter
Keyword(s):  
Young Adult ◽  
Qualitative Study ◽  
Identity Formation ◽  
Adult Daughters ◽  
Lesbian Mothers

Band-Aids and Kisses Can’t Fix It: Mothers’ and Daughters’ Perceptions of Non-Death Loss and Boundary Ambiguity

2020 ◽  
pp. 105413732096848
Author(s):  
Kathryn E. Bojczyk ◽  
Heather R. Haverback
Keyword(s):  
Young Adult ◽  
Qualitative Study ◽  
Adult Daughters ◽  
Mothers And Daughters ◽  
Individual Interviews ◽  
Boundary Ambiguity ◽  
Mother Daughter Relationship ◽  
Convergence And Divergence ◽  
The Individual ◽  
The Impact

The goal of this study was to explore middle aged mothers’ and young adult daughters’ perceptions of the impact of non-death loss. This qualitative study explored perceptions of loss and boundary ambiguity of 24 mother-daughter dyads through individual interviews. All mothers and daughters described losses such as illness, the daughters’ launching, and dissolution of relationships that impacted the mother-daughter relationship. Comparison of mothers’ and daughters’ descriptions of the impacts of loss revealed convergence and divergence in their descriptions of associated levels of boundary ambiguity. Although experiences of loss do seem to be a universal human experience, perceptions regarding the impact of loss on both the individual and the mother-daughter dyad vary greatly.

Navigating being a young adult with cerebral palsy: a qualitative study

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Gitte Normann ◽  
Kirsten Arntz Boisen ◽  
Peter Uldall ◽  
Anne Brødsgaard
Keyword(s):  
Young Adults ◽  
Cerebral Palsy ◽  
Young Adult ◽  
Qualitative Study ◽  
Healthcare System ◽  
Young Adulthood ◽  
Educational Background ◽  
Pediatric Care ◽  
Healthcare Needs ◽  
New Challenges

AbstractObjectivesYoung adults with cerebral palsy (CP) face potential challenges. The transition to young adulthood is characterized by significant changes in roles and responsibilities. Furthermore, young adults with chronic conditions face a transfer from pediatric care to adult healthcare. This study explores how living with CP affects young adults in general, and specifically which psychosocial, medical and healthcare needs are particularly important during this phase of life.MethodsA qualitative study with data from individual, semi-structured, in-depth interviews with six young adults with CP (ages 21–31 years) were transcribed verbatim and analyzed. The participants were selected to provide a maximum variation in age, gender, Gross Motor Function Classification System score and educational background. A descriptive thematic analysis was used to explore patterns and identify themes.ResultsThree themes were identified: “Being a Young Adult”, “Development in Physical Disability and New Challenges in Adulthood” and “Navigating the Healthcare System”. The three themes emerged from 15 sub-themes. Our findings emphasized that young adults with CP faced psychosocial challenges in social relationships, participation in education and work settings and striving towards independence. The transition to young adulthood led to a series of new challenges that the young adults were not prepared for. Medical challenges included managing CP-related physical and cognitive symptoms and navigating adult health care services, where new physicians with insufficient knowledge regarding CP were encountered.ConclusionThe young adults with CP were not prepared for the challenges and changes they faced during their transition into adulthood. They felt that they had been abandoned by the healthcare system and lacked a medical home. Better transitional care is urgently needed to prepare them for the challenges in young adulthood.

scholarly journals The experiences and strategies of parents’ of adults with anorexia nervosa or bulimia nervosa: a qualitative study

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Jannike Karlstad ◽  
Cathrine Fredriksen Moe ◽  
Mari Wattum ◽  
Berit Støre Brinchmann
Keyword(s):  
Eating Disorders ◽  
Anorexia Nervosa ◽  
Qualitative Study ◽  
Health Services ◽  
Bulimia Nervosa ◽  
Professional Support ◽  
Adult Daughters ◽  
Main Concern ◽  
The Core ◽  
Core Category

Abstract Background Caring for an individual with an eating disorder involves guilt, distress and many extra burdens and unmet needs. This qualitative study explored the experiences of parents with adult daughters suffering from anorexia nervosa or bulimia nervosa and the strategies they adopted. A subsidiary aim of the study was to explore the relationship between the caregivers’ perceived need for professional support and the support they reported receiving in practice from the health services. Methods Semi-structured interviews were conducted with 11 mothers and fathers from across Norway. Data collection, coding and analysis was conducted using the principles of constructivist grounded theory in an iterative process. The main concern shared by participants was identified by this process and their “solution” to the main concern then formed the content of the core category. Results ″Wearing all the hats″ emerged as the core category, indicating that the parents have to fulfil several roles to compensate the lack of help from health services. The three subcategories: “adapting to the illness”, “struggling for understanding and help” and “continuing to stay strong” described how the participants handled their situation as parents of adult daughters with eating disorders. Conclusions In daily life, the parents of adults with eating disorders have to attend to a wide range of caregiver tasks to help their ill daughters. This study suggests that the health services that treat adults with eating disorders should be coordinated, with a professional carer in charge. The parents need easy access to information about the illness and its treatment. They also need professional support for themselves in a demanding situation.

Adolescent and Young Adult Cancer Survivors' Experiences of the Healthcare System: A Qualitative Study

2018 ◽  
Vol 7 (1) ◽  
pp. 88-96 ◽  
Author(s):  
Elizabeth A. May ◽  
Brittany C. McGill ◽  
Eden G. Robertson ◽  
Antoinette Anazodo ◽  
Claire E. Wakefield ◽  
...  
Keyword(s):  
Young Adult ◽  
Qualitative Study ◽  
Cancer Survivors ◽  
Healthcare System ◽  
Adolescent And Young Adult ◽  
Young Adult Cancer Survivors ◽  
System A ◽  
Adult Cancer Survivors ◽  
Young Adult Cancer

Factors that promote and impede other-sex friendships: a qualitative study of Iranian adolescent girls

2016 ◽  
Vol 30 (4) ◽  
Author(s):  
Nasim Bahrami ◽  
Masoumeh Sibmar ◽  
William M. Bukowski ◽  
AbouAli Vedadhir ◽  
Bianca Panarello
Keyword(s):  
Qualitative Study ◽  
Identity Formation ◽  
Adolescent Girls ◽  
Qualitative Content Analysis ◽  
Self Esteem ◽  
Structured Interviews ◽  
Public Places ◽  
Self Confidence ◽  
Poor Understanding ◽  
Different Levels

Abstract Aim: The aim of this study was to identify factors that promote and impede other-sex (OS) friendships in adolescent girls. Methods: A qualitative study conducted with 20 adolescent girls recruited in public places in Tehran, Iran. Information was collected through semi-structured interviews and coded via the conventional qualitative content analysis approach. Results: Four factors were identified that appeared to promote entry into OS friendships. These factors include (a) a poor understanding of perceived risks, (b) weak religious beliefs, (c) processes of identity formation, and (d) low self-esteem. In addition, six factors appeared to impede entry into these friendships: (a) self-confidence, (b) prioritizing education, (c) maintaining particular entertainment preferences, (d) awareness of prior unpleasant experiences with boys, (e) having strong religious convictions, and (f) shaming from significant others. Conclusion: These findings provide unique insights into the factors that stem from different levels of social complexity, which affect participation in a fundamental form of human experience.

scholarly journals A qualitative study of adolescent and young adult cancer survivors’ perceptions of family and peer support

2018 ◽  
Vol 25 (5) ◽  
pp. 713-726 ◽  
Author(s):  
Glynnis A McDonnell ◽  
Elyse Shuk ◽  
Jennifer S Ford
Keyword(s):  
Young Adult ◽  
Qualitative Study ◽  
Peer Support ◽  
Adult Survivors ◽  
Adolescent And Young Adult ◽  
Structured Interviews ◽  
Young Adult Cancer Survivors ◽  
Practical Support ◽  
Adult Cancer Survivors ◽  
Young Adult Survivors

This qualitative study examined adolescent and young adult survivors’ perceptions of support from family and peers. A total of 26 survivors, aged 16–24 years, who had been diagnosed with cancer between the ages of 14 and 18, participated in semi-structured interviews. Three themes emerged for support: practical support, emotional support, and new sense of closeness. For lack of support, two themes emerged: absence during treatment and lack of understanding about appearance changes. These findings emphasize the perceived importance of family and peer support throughout adolescent and young adults’ cancer trajectories and indicate a need for interventions to help adolescent and young adult develop and maintain support networks throughout treatment and survivorship.

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