scholarly journals Women’s experiences of self-administration of misoprostol at home as part of early medical abortion: a qualitative evaluation

2020 ◽  
pp. bmjsrh-2020-200661 ◽  
Author(s):  
Jeni Harden ◽  
Julie Ancian ◽  
Sharon Cameron ◽  
Nicola Boydell
Keyword(s):  
Clinical Setting ◽  
Qualitative Interviews ◽  
Qualitative Evaluation ◽  
Medical Abortion ◽  
Self Administration ◽  
Women’S Experiences ◽  
Women's Experiences ◽  
The Uk ◽  
Experiences Of Women ◽  
At Home

BackgroundBetween 2017 and 2019, legislation was introduced in the UK that approved the home as a place for self-administration of misoprostol for early medical abortion. While research has shown that early medical abortion at home is as safe as in a clinical setting, women’s experiences in the UK in the light of this change have not yet been investigated. This qualitative research explored the experiences of women in one region of Scotland, UK who accessed early medical abortion with home self-administration of misoprostol.MethodsQualitative interviews were conducted with 20 women who had recently undergone early medical abortion (≤69 days' gestation) with home self-administration of misoprostol. The data were analysed thematically using an approach informed by the Framework analytic approach.ResultsWomen appreciated the flexibility that home administration of misoprostol offered, including the opportunity to control the timing of the abortion. This was particularly important for women who sought not to disclose the abortion to others. Most women valued being in the comfort and privacy of the home when preparing for self-administration, although a small number highlighted some concerns about being at home. Most women reported that self-administration of misoprostol was straightforward; however, some expressed concerns around assessing whether their experiences were ‘normal’.ConclusionsWomen welcomed the opportunity for home self-administration of misoprostol. To further improve women’s early medical abortion experience we suggest that the legislation be amended so that women can self-administer in an appropriate non-clinical setting, not just their home.

Women's experiences of having an early medical abortion at home

2016 ◽  
Vol 9 ◽  
pp. 48-54 ◽  
Author(s):  
Maria Hedqvist ◽  
Lina Brolin ◽  
Tanja Tydén ◽  
Margareta Larsson
Keyword(s):  
Medical Abortion ◽  
Women’S Experiences ◽  
Women's Experiences ◽  
At Home

scholarly journals Dispositions that matter: Investigating criminalized women’s resettlement through their (trans)carceral habitus

2021 ◽  
pp. 174889582110173
Author(s):  
Kaitlyn Quinn
Keyword(s):  
Public Health ◽  
Qualitative Research ◽  
Social Justice ◽  
Health Safety ◽  
Women’S Experiences ◽  
Women's Experiences ◽  
Theoretical Innovation ◽  
The Impact ◽  
Experiences Of Women ◽  
Feminist Work

Whether prisoner resettlement is framed in terms of public health, safety, economic prudence, recidivism, social justice, or humanitarianism, it is difficult to overstate its importance. This article investigates women’s experiences exiting prison in Canada to deepen understandings of post-carceral trajectories and their implications. It combines feminist work on transcarceration and Bourdieusian theory with qualitative research undertaken in Canada to propose the (trans)carceral habitus as a theoretical innovation. This research illuminates the continuity of criminalized women’s marginalization before and beyond their imprisonment, the embodied nature of these experiences, and the adaptive dispositions that they have demonstrated and depended on throughout their lives. In doing so, this article extends criminological work on carceral habitus which has rarely considered the experiences of women. Implications for resettlement are discussed by tracing the impact of criminalized women’s (trans)carceral habitus (i.e. distrust, skepticism, vigilance about their environments and relationships) on their willingness to access support and services offered by resettlement organizations.

‘You don’t look autistic’: A qualitative exploration of women’s experiences of being the ‘autistic other’

Autism ◽  
2021 ◽  
pp. 136236132199372
Author(s):  
Kate Seers ◽  
Rachel C Hogg
Keyword(s):  
Lived Experiences ◽  
Well Being ◽  
Autism Spectrum ◽  
Social Expectations ◽  
Autism Spectrum Condition ◽  
Women’S Experiences ◽  
Women's Experiences ◽  
Spectrum Condition ◽  
The Impact ◽  
Experiences Of Women

There is currently a paucity of literature exploring the experiences of women on the autism spectrum. It is imperative research is conducted to capture the experiences of women on the autism spectrum and ensure appropriate support is provided to this cohort. Drawing upon a social constructionist framework, this qualitative research study sought to understand how psychological and socio-cultural constructions of autism spectrum condition and gender influence the well-being of women on the autism spectrum. Eight participants engaged in a semi-structured interview, with thematic analysis conducted to demonstrate the impact of gender roles and social expectations on the women’s identity and autism spectrum condition expression. The research highlighted the changing understandings of autism spectrum condition across a woman’s lifespan and the process and impact of resisting hegemonic autism spectrum condition categorisation. The findings demonstrate that social constructions of gender and stereotypical understandings of autism spectrum condition, which prioritise a deficit, medical model, have significant consequences for women’s well-being and subjectivity. The women experienced challenging formative years, but with diagnosis and the evolution and acceptance of their identities, they were able to resist negative narratives of autism spectrum condition, embrace their strengths and develop adaptive coping strategies. It is hoped this article generates insights for societal and clinical recognition to better support women on the autism spectrum. Lay abstract Most autism spectrum condition research addresses the neurological and biological causes of autism spectrum condition, focusing upon deficits associated with autism spectrum condition and behavioural interventions designed to minimise these deficits. Little is known about the lived experiences of adult women on the autism spectrum and how they navigate social expectations around gender, autism spectrum condition and gendered understandings of autism spectrum condition. The lived experiences of eight women on the AS will be shared here, with attention to how gendered expectations influence women’s experiences of autism spectrum condition, their sense of self and well-being. Findings showed these women struggled to reconcile the expectations of others, particularly early in life. The women had difficultly conforming to stereotypical ideals of femininity, yet as they aged, they felt less need to conform, valuing their unique style and behaviours. The women also rejected deficit-oriented descriptions of autism spectrum condition generated by the medical community, preferring to focus on their strengths and unique characteristics. It is hoped this article helps psychologists and the wider community to understand and meet the needs of women on the AS.

scholarly journals Neglected bodily senses in women living with vertebral fracture: a focus group study

Rheumatology ◽  
2019 ◽  
Vol 59 (2) ◽  
pp. 379-385 ◽  
Author(s):  
Sarah Drew ◽  
Emma Clark ◽  
Usama Al-Sari ◽  
Andrew Moore ◽  
Rachael Gooberman-Hill
Keyword(s):  
Vertebral Fracture ◽  
Screening Tool ◽  
Fear Of Falling ◽  
Body Parts ◽  
Focus Group Study ◽  
Women’S Experiences ◽  
Women's Experiences ◽  
Spinal Radiograph ◽  
Qualitative Focus Groups ◽  
Experiences Of Women

Abstract Objective Older women are at particular risk of osteoporosis. Among women with osteoporosis, fractures of the vertebra (vertebral fracture) are common, hard to detect and associated with risk of further fracture. Identifying vertebral fracture in a timely manner allows instigation of preventive measures to reduce the risk of further fracture. Although detection of vertebral fracture requires spinal radiograph, many women do not receive referral. To begin development of a screening tool to identify women in need of referral we undertook a qualitative study to characterize women’s experiences of vertebral fracture, using Eccleston’s ‘Ten Neglected Bodily Senses’. Methods Four qualitative focus groups were conducted with women who had been diagnosed with vertebral fracture (n = 19, age 60–91 years). Data were audio-recorded, transcribed and analysed thematically using the ‘Ten Neglected Bodily Senses’. Results Women’s experiences of vertebral fractures related to seven senses: pain, movement, fatigue, balance, pressure, appetite and breathing. Pain was the dominant sense and all participants explained how pain increased with activity, reaching a crescendo, and described strategies to minimize this disruption. Most participants had become physically shorter, making some feel ‘squashed’, putting pressure on other body parts. Some described appetite loss or a sense of restricted breathing. Participants experienced a sense of being ‘pulled’ forwards, impacting on balance and exacerbating fear of falling. Conclusion The study found senses that have not been previously described in the experiences of women with vertebral fracture. These will be used to inform the design of a new screening tool for use in primary care.

Expanding medical abortion in Tunisia: women's experiences from a multi-site expansion study

Contraception ◽  
2004 ◽  
Vol 70 (6) ◽  
pp. 487-491 ◽  
Author(s):  
Selma Hajri ◽  
Jennifer Blum ◽  
Nabiha Gueddana ◽  
Habib Saadi ◽  
Leila Maazoun ◽  
...  
Keyword(s):  
Medical Abortion ◽  
Women’S Experiences ◽  
Women's Experiences

Understanding women's experiences with medical abortion: In-depth interviews with women in two Indian clinics

2010 ◽  
Vol 5 (4) ◽  
pp. 335-347 ◽  
Author(s):  
B. Ganatra ◽  
S. Kalyanwala ◽  
B. Elul ◽  
K. Coyaji ◽  
S. Tewari
Keyword(s):  
Medical Abortion ◽  
Women’S Experiences ◽  
Women's Experiences ◽  
Depth Interviews

It's No Life, This Fear' Women's Experiences of Services when in Situations of Family Violence

1999 ◽  
Vol 5 (1) ◽  
pp. 53
Author(s):  
Kim Robinson
Keyword(s):  
Social Welfare ◽  
Knowledge Base ◽  
Family Violence ◽  
Service Providers ◽  
Service System ◽  
Waiting Lists ◽  
Women’S Experiences ◽  
Women's Experiences ◽  
Experiences Of Women

This study examines the experiences of women who have been in situations of family violence, and identifies the barriers they faced when seeking assistance from a variety of services. The research aims to contribute to the knowledge base of the health, social welfare, legal and policing services which respond to calls for assistance from women faced with family violence. The service system is varied in how it conceptualizes family violence, and in the aims of the services it provides. The research reports that the service system does not always meet the needs of victim/survivors, and reveals that service providers are often ill equipped to deal with the complexity of violence. Due to the length of waiting lists and the quality of interventions women experienced particular difficulty in accessing advice based services. A number of recommendations are made for improvements in services.

Sign in / Sign up

Export Citation Format

Share Document