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Åkeflo, L., Elmerstig, E., Bergmark, K. & Dunberger, G. (2023). Barriers to and strategies for dealing with vaginal dilator therapy - Female pelvic cancer survivors' experiences: A qualitative study. European Journal of Oncology Nursing, 62, Article ID 102252.
Open this publication in new window or tab >>Barriers to and strategies for dealing with vaginal dilator therapy - Female pelvic cancer survivors' experiences: A qualitative study
2023 (English)In: European Journal of Oncology Nursing, ISSN 1462-3889, E-ISSN 1532-2122, Vol. 62, article id 102252Article in journal (Refereed) Published
Abstract [en]

PURPOSE: Vaginal changes, a frequently reported late effect among women treated with pelvic radiotherapy, can result in sexual dysfunction and distress. Women are recommended vaginal dilator therapy after completed radiotherapy; however, low adoption has been recognized. This study aims to provide insight into women's difficulties with carrying out vaginal dilator therapy and their experiences of information.

METHODS: Face-to-face, semi-structured interviews were undertaken with 12 pelvic cancer survivors in a selected sample of women with difficulties adopting the therapy. Interviews were audio-recorded, transcribed and analyzed using qualitative content analysis.

RESULTS: One overarching theme, Being unprepared, emerged from three identified categories relating to Experience of received information, Experience of performing the therapy, and Motivation to perform the therapy. The women experienced the information as unrealistic and insufficient, and requested clearer and earlier information. Bleeding, pain, fear of cancer recurrence, and recalling memories from treatments were experienced. Women described intestinal symptoms, fatigue, and feeling that the therapy was self-harm as barriers to performing the therapy. They described creating routines, breathing exercises, relaxation, pre-warming the dilator and performing therapy together with their partner as helpful strategies.

CONCLUSIONS: Careful discussion, early and clear communication, psychoeducation and supportive follow-up of vaginal changes should be integrated into cancer treatment and follow up. Healthcare professionals should be aware of potential difficulties with vaginal dilator therapy and identify women in need of extended support. Research is required to investigate interventions that suit the needs of female pelvic cancer survivors.

Place, publisher, year, edition, pages
Elsevier, 2023
Keywords
Female cancer survivor, Late effect, Pelvic radiotherapy, Vaginal dilator therapy, Vaginal stenosis
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:mau:diva-58507 (URN)10.1016/j.ejon.2022.102252 (DOI)000975520100001 ()36603495 (PubMedID)2-s2.0-85145728479 (Scopus ID)
Available from: 2023-03-02 Created: 2023-03-02 Last updated: 2023-12-13Bibliographically approved
Löfgren, C., Elmerstig, E., Schröder, J., Chollier, M., Mehulic, J., de Graaf, H., . . . Stulhofer, A. (2023). Changes in Intimacy and Sexuality During the COVID-19 Pandemic: A Qualitative Analysis of Data from a Survey on Partnered Individuals in Eight European Countries. Sexuality & Culture, 27(2), 693-714
Open this publication in new window or tab >>Changes in Intimacy and Sexuality During the COVID-19 Pandemic: A Qualitative Analysis of Data from a Survey on Partnered Individuals in Eight European Countries
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2023 (English)In: Sexuality & Culture, ISSN 1095-5143, E-ISSN 1936-4822, Vol. 27, no 2, p. 693-714Article in journal (Refereed) Published
Abstract [en]

This qualitative study explores experiences of intimacy and sexuality during the first phase of the COVID-19 pandemic of 3357 participants from Croatia, the Czech Republic, the Netherlands, France, Germany, Portugal, Sweden, and Turkey. Data were collected through open-ended questions within a survey on sexuality during the pandemic. Based on a reflexive thematic analysis three themes occurred. The first theme No change was described by 41% when summarizing their sex life during the pandemic. The second theme Positive change was experienced by 25%, and the third theme Negative change by 21%. An overarching theme then emerged as: "Still the same trajectories, but the pandemic could be a catalyst for improved or worsened sex- life." For those intimate partnered individuals who already had problems with intimacy and sexuality before the COVID-19 pandemic it seemed to remain the same or deteriorated throughout the pandemic. For those with positive experiences of intimacy and sexuality before the COVID-19 pandemic it remained the same or improved throughout the pandemic. These findings are relevant for researchers and clinicians in developing preventive and supportive interventions in the context of crisis and social isolation.

Place, publisher, year, edition, pages
Springer, 2023
Keywords
COVID-19, Reflexive thematic analysis, Adults, Relationship satisfaction, Sexual health, Intimacy
National Category
Public Health, Global Health, Social Medicine and Epidemiology
Identifiers
urn:nbn:se:mau:diva-56040 (URN)10.1007/s12119-022-10035-1 (DOI)000874396000001 ()36320864 (PubMedID)2-s2.0-85140825046 (Scopus ID)
Available from: 2022-11-16 Created: 2022-11-16 Last updated: 2023-09-07Bibliographically approved
Ek, A.-S., Holmström, C. & Elmerstig, E. (2023). Sexuality >1 year after brain injury rehabilitation: A cross-sectional study in Sweden. Brain Injury, 37(1), 34-46
Open this publication in new window or tab >>Sexuality >1 year after brain injury rehabilitation: A cross-sectional study in Sweden
2023 (English)In: Brain Injury, ISSN 0269-9052, E-ISSN 1362-301X, Vol. 37, no 1, p. 34-46Article in journal (Refereed) Published
Abstract [en]

PURPOSE: This study investigates whether Acquired Brain Injury (ABI) is associated with changes in sexual function and satisfaction and how such changes are experienced, focusing on invisible impairments after ABI.

MATERIALS AND METHODS: A study-specific questionnaire was distributed in 2018-2019. The sample included individuals aged 20-90 years diagnosed with ABI due to subarachnoid hemorrhage (SAH), trauma, infection, or anoxia (ischemic stroke and intracerebral hemorrhage excluded), who participated in brain injury rehabilitation in Sweden, 2014-2016. Chi-square and Logistic regression analyses were used.

RESULTS: The study consists of 250 participants (response rate was 40%). Among participants 78% (194/250) had resumed sexual life. Participants reporting sexual changes also experienced more consequences related to ABI. Those with decreased sexual desire (63%, 148/234) reported more ABI consequences, including decreased memory (86% vs 65%, p = 0.000), decreased concentration ability (82% vs 65%, p = 0.003), and increased tiredness (91% vs 70%, p = 0.000) compared to those with intact desire. Such consequences can be invisible to others.

CONCLUSION: Visible impairments are known to impact sexual functions and satisfaction after ABI. Our results show how invisible impairments also have a great impact. From a biopsychosocial perspective, these results imply that individuals should receive sexual rehabilitation, irrespective of ABI impairment.

Place, publisher, year, edition, pages
Taylor & Francis, 2023
Keywords
Acquired brain injury, biopsychosocial, neurosexuality, rehabilitation, sexuality
National Category
Neurology
Identifiers
urn:nbn:se:mau:diva-56604 (URN)10.1080/02699052.2022.2145358 (DOI)000888468400001 ()36408962 (PubMedID)2-s2.0-85142431595 (Scopus ID)
Available from: 2022-12-13 Created: 2022-12-13 Last updated: 2024-02-05Bibliographically approved
Bodin, M., Plantin, L., Schmidt, L., Ziebe, S. & Elmerstig, E. (2023). The pros and cons of fertility awareness and information: a generational, Swedish perspective. Human Fertility, 26(2), 216-225
Open this publication in new window or tab >>The pros and cons of fertility awareness and information: a generational, Swedish perspective
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2023 (English)In: Human Fertility, ISSN 1464-7273, E-ISSN 1742-8149, Vol. 26, no 2, p. 216-225Article in journal (Refereed) Published
Abstract [en]

Being aware of factors that affect fertility can help people make informed decisions about their reproductive futures. To some, however, fertility information leads to worry and self-blame. In this paper, we explore how people from different generations discuss fertility and reproductive decision-making, along with their perceptions of fertility information. The study was conducted in southern Sweden with 26 focus-group discussions that included a total of 110 participants aged 17-90 years. The material was analysed thematically. Our results show that fertility knowledge and openness to talking about fertility problems have increased over generations. Participants who were assigned female at birth were more often concerned about their fertility than those who were not, and fertility concerns were transferred from mothers to daughters. While age-related fertility concerns had been uncommon in older generations, participants aged 25-40 often expressed these concerns. Young adults appreciated being knowledgeable about fertility but simultaneously expressed how fertility information could lead to distress. Our conclusion is that fertility information was best received by high-school students, and efforts to improve fertility education in schools are therefore recommended.

Place, publisher, year, edition, pages
Taylor & Francis, 2023
Keywords
Fertility awareness, reproductive decision-making, generations, focus group discussions
National Category
Obstetrics, Gynecology and Reproductive Medicine
Identifiers
urn:nbn:se:mau:diva-45816 (URN)10.1080/14647273.2021.1968045 (DOI)000687543600001 ()34423731 (PubMedID)2-s2.0-85113809500 (Scopus ID)
Available from: 2021-09-15 Created: 2021-09-15 Last updated: 2023-12-07Bibliographically approved
Palm, C., Elmerstig, E., Holmström, C. & Essen, B. (2023). The relationship between dominant Western discourse and personal narratives of female genital cutting: exploring storytelling among Swedish-Somali girls and women. Frontiers in Sociology, 8, Article ID 1188097.
Open this publication in new window or tab >>The relationship between dominant Western discourse and personal narratives of female genital cutting: exploring storytelling among Swedish-Somali girls and women
2023 (English)In: Frontiers in Sociology, E-ISSN 2297-7775, Vol. 8, article id 1188097Article in journal (Refereed) Published
Abstract [en]

Introduction: A dominant narrative, referred to as “the standard tale,” prevails in popular representations about female genital cutting (FGC) that often contrast with how cut women traditionally narrate their FGC experience as meaningful in contexts where FGC is customary. However, scholarship has increasingly highlighted how global eradication campaigns and migration to countries where FGC is stigmatized provide women with new frames of understanding which may lead to a reformulation of previous experiences. This article subjects the storytelling itself to analysis and explores how participants narrate and make sense of their FGC experience in a post-migration setting where FGC is stigmatized.

Methods: Semi-structured focus groups (9) and individual interviews (12) with Swedish-Somali girls and women (53) were conducted.

Results: The article highlights how the participants navigate their storying in relation to "the standard tale" of FGC in their efforts to make sense of their experiences. Navigation was conducted both at an intrapersonal level through continuous identity work, and in relation to the social context in interpersonal encounters, i.e., with service providers and others, among whom the standard tale has become a truth.

Discussion: The article places the analysis within broader discussions about anti-FGC work and considers the implications in relation to efforts to end FGC.

Place, publisher, year, edition, pages
Frontiers Media S.A., 2023
Keywords
female genital cutting, female genital mutilation, anti-FGM discourse, migration, storytelling, qualitative research
National Category
Social Work
Identifiers
urn:nbn:se:mau:diva-61891 (URN)10.3389/fsoc.2023.1188097 (DOI)001032417000001 ()37497100 (PubMedID)2-s2.0-85165699987 (Scopus ID)
Available from: 2023-08-16 Created: 2023-08-16 Last updated: 2024-03-26Bibliographically approved
Ek, A.-S., Holmström, C. & Elmerstig, E. (2023). Unmet Need for Sexual Rehabilitation after Acquired Brain Injury (ABI): A Cross-Sectional Study Concerning Sexual Activity, Sexual Relationships, and Sexual Rehabilitation after ABI. Sexuality and disability, 41(2), 387-410
Open this publication in new window or tab >>Unmet Need for Sexual Rehabilitation after Acquired Brain Injury (ABI): A Cross-Sectional Study Concerning Sexual Activity, Sexual Relationships, and Sexual Rehabilitation after ABI
2023 (English)In: Sexuality and disability, ISSN 0146-1044, E-ISSN 1573-6717, Vol. 41, no 2, p. 387-410Article in journal (Refereed) Published
Abstract [en]

In relation to brain injury rehabilitation, research has stressed the importance of including sexuality issues due to increased risk for sexual dysfunctions after Acquired Brain Injury (ABI). This study aims to explore experiences after non-stroke ABI concerning individual and relational aspects of sexuality, received information about sexuality at rehabilitation, and gender differences. A postal nationwide survey was conducted in Sweden, 2018-2019. The sample included individuals who had participated in brain injury rehabilitation 2014-2016, response rate 40% (250/624). Among all participants 78% had resumed sexual activity, and there was a significant difference between males (84%, 118/140) and females (69%, 76/110, p = 0.004). Among all participants, 95% reported physical intimacy as important, 80% considered sex as important on an individual level, and 91% stated sexuality as important for the relationship (no gender differences). Significantly more females (52%) than males (22%) reported that they had tried sexual aids (p = 0.000), and more males (29%) than females (16%) reported that professionals addressed sexuality issues during brain injury rehabilitation (p = 0.024). However, only a few participants were offered specific sexual counseling during brain injury rehabilitation, such as individual counseling (3%), couples counseling (2%), and group counseling (3%). To conclude, the vast majority valued both individual and relational aspects of sex and sexuality highly, and more males than females had resumed sexual activity. Few had received information about sexuality after ABI, and even fewer females compared to males reported that the issue was raised during rehabilitation. Clinical implications are discussed in relation to sexual rehabilitation.

Place, publisher, year, edition, pages
Springer, 2023
Keywords
Acquired brain injury, Sexuality, Rehabilitation, Counseling, Relationship, Gender, Sweden
National Category
Health Sciences
Identifiers
urn:nbn:se:mau:diva-59489 (URN)10.1007/s11195-023-09788-w (DOI)000962026300001 ()2-s2.0-85151422464 (Scopus ID)
Available from: 2023-05-15 Created: 2023-05-15 Last updated: 2023-10-18Bibliographically approved
Palm, C., Johnsdotter, S., Elmerstig, E., Holmström, C. & Essén, B. (2022). Adolescent Sexual and Reproductive Health Counselling in Relation to Female Genital Cutting: Swedish Professionals' Approach to Menstrual Pain as an Empirical Example. Sexuality & Culture, 26, 1-25
Open this publication in new window or tab >>Adolescent Sexual and Reproductive Health Counselling in Relation to Female Genital Cutting: Swedish Professionals' Approach to Menstrual Pain as an Empirical Example
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2022 (English)In: Sexuality & Culture, ISSN 1095-5143, E-ISSN 1936-4822, Vol. 26, p. 1-25Article in journal (Refereed) Published
Abstract [en]

In Sweden, as well as in an international context, professionals are urged to acquire knowledge about possible health effects of female genital cutting (FGC) in order to tackle prevention and care in relation to the practice. While professionals are guided by policies and interventions focusing on medical effects of FGC, some scholars have cautioned that many popular beliefs about health risks rest on inconclusive evidence. The way professionals understand and respond to health information about FGC has in this context largely been left unexamined. This article aims to provide a qualitative exploration of how professionals in Sweden approach adolescent sexual and reproductive healthcare encounters in relation to acquired knowledge about FGC, using menstrual pain as an empirical example. The analysis shows that there was a tendency in counselling to differentiate young migrant women's menstrual complaints from ordinary menstrual pain, with professionals understanding pain complaints either in terms of FGC or as culturally influenced. The study shows how professionals navigated their various sources of knowledge where FGC awareness worked as a lens through which young women's health complaints were understood. Biomedical knowledge and culture-specific expectations and assumptions regarding menstrual pain also informed counselling. Finally, the article discusses how FGC awareness about health risks was used constructively as a tool to establish rapport and take a history on both menstrual pain and FGC. The analysis also recognises potential pitfalls of the approaches used, if not based in well-informed policies and interventions in the first place.

Place, publisher, year, edition, pages
Springer, 2022
Keywords
Female genital cutting, Sexual and reproductive health counselling, Menstrual pain, Migration, Youth, Sweden
National Category
Public Health, Global Health, Social Medicine and Epidemiology
Research subject
Health and society
Identifiers
urn:nbn:se:mau:diva-44875 (URN)10.1007/s12119-021-09895-w (DOI)000673518600001 ()2-s2.0-85122382469 (Scopus ID)
Available from: 2021-08-17 Created: 2021-08-17 Last updated: 2024-03-26Bibliographically approved
Holmström, C., Plantin, L. & Elmerstig, E. (2022). Complexities of sexual consent: Young people's reasoning in a Swedish context. In: Malachi Willis (Ed.), Nuances of Sexual Consent: (pp. 77-92). Routledge
Open this publication in new window or tab >>Complexities of sexual consent: Young people's reasoning in a Swedish context
2022 (English)In: Nuances of Sexual Consent / [ed] Malachi Willis, Routledge, 2022, p. 77-92Chapter in book (Refereed)
Abstract [en]

Although previous research and public debate argue that partnered sexual activity is construed in terms of being consensual or not, we know little about young people’s own reasoning on sexual consent. This study aimed to investigate how sexual consent and sexual negotiations are interpreted by young people in Sweden. Forty-four female and male participants, ranging from 18–21 years old, took part in 12 focus groups, organised according to a set of vignettes. All focus groups were analysed using inductive thematic analysis. The findings illustrate the complexity of the interpretation of sexual consent. There was a clear perception among the participants that sex between two individuals is a mutual process, and that sex should be consensual, expressed either through words, body language, or both. They all stated clearly that a ‘No’ has to be respected, independently of context. However, at the same time participants expressed contradictory norms and expectations in relation to the described situations, that showed an ambivalence concerning sexual scripts and consequences of challenging these in specific situations. Reasoning concerning discrepancy between ideals and actual possibilities to act in sexual encounters indicates differences in relation to gender, age and educational background and pathways.

Place, publisher, year, edition, pages
Routledge, 2022
National Category
Law and Society
Identifiers
urn:nbn:se:mau:diva-63383 (URN)10.4324/9781003276180-6 (DOI)9781003276180 (ISBN)9781032231860 (ISBN)
Note

Previously published as Charlotta Holmström, Lars Plantin & Eva Elmerstig (2020) Complexities of sexual consent: young people’s reasoning in a Swedish context, Psychology & Sexuality, 11:4, 342-357, DOI: 10.1080/19419899.2020.1769163

Available from: 2023-11-02 Created: 2023-11-02 Last updated: 2023-11-02Bibliographically approved
Hall, I. E., Holmström, C., Bodin, M., Schmidt, L., Ziebe, S. & Elmerstig, E. (2022). Experiences of involuntary childlessness during the COVID-19 pandemic. In: ESC Abstract Book 2022: . Paper presented at 16th ESCRH2022 Congress of the European Society of Contraception and Reproductive Health, Ghent, Belgium, May 25-28, 2022.. The European Society of Contraception and Reproductive Health (ESC)
Open this publication in new window or tab >>Experiences of involuntary childlessness during the COVID-19 pandemic
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2022 (English)In: ESC Abstract Book 2022, The European Society of Contraception and Reproductive Health (ESC) , 2022Conference paper, Oral presentation with published abstract (Refereed)
Abstract [en]

BACKGROUND

The overall purpose is to investigate how the COVID-19 pandemic has affected individuals who have been or are going through assessment or treatment for involuntary childlessness, and their processes of trying to have children. Previous research on involuntary childlessness in relation to the pandemic has mainly been medical and quantitative, and there has been a lack of qualitative studies that explore the subject area on a more indepth level. The study is a project in ReproUnion, Challenge 5.

MATERIALS AND METHODS

In this qualitative study, we used semistructured interviews to collect data. The study includes individuals who have been or are going through assessment or treatment for involuntary childlessness in Sweden and Denmark during the pandemic. Participants were recruited from both public and private care. 26 individuals took part in the study, of which 18 women and eight men. The participants were between 24 53 years old and the sample consisted of both heterosexual and same sex couples. The interviews addressed experiences of assessment and treatment of involuntary childlessness during the COVID-19 pandemic in relation to e.g.access to care, socioeconomic factors and intimate relationships.

RESULTS AND CONCLUSION

The preliminary results show that the pandemic has affected the patients in many ways and made an already challenging process even more difficult.Obstacles mentioned are for example limit access to care with longer queues and uncertainty regarding when the treatment can be resumed. Many of the respondents has also suffered from the absence of partners during care visits. Furthermore, the fear of being infected by the Corona virus, which could cause the treatment to be postponed, has led to isolation and often a weaker support from family and friends. However, these negative consequences have affected patients to varying degrees, some worse than others. The results also show that the pandemic brought some positive consequences. For example, the isolation has been perceived as a relief for some as they easier could avoid being exposed to other people’s pregnancies as well as attending baptisms and baby showers.

“It has been extremely stressful for me to hear those messages [about delays of the treatment from the clinic], as it has taken so long to get started , and, yes, I am not getting any younger. That's how I feel. For every six months that goes by, I have kind of lost a chance to get pregnant.”

"We are young and have no underlying health problems, but we still really had to isolate ourselves, and we were very afraid that we would catch a cold or suffer from Corona so that the treatments would be cancelled. So, it was all the time that you were afraid to meet people, and you were afraid to meet your friends”

“I think the biggest impact was that I was not allowed to accompany and that I was not allowed to participate, also in combination with this stress that you could get sick. That was probably thebiggest impact for me and my wife.”

CONTACT

Ida Elisabet Hall

Research assistant, social worker, master in sexology

Centre for Sexology and Sexuality Studies, Malmö University

ida.hall@mau.se

Place, publisher, year, edition, pages
The European Society of Contraception and Reproductive Health (ESC), 2022
National Category
Other Health Sciences
Research subject
Health and society
Identifiers
urn:nbn:se:mau:diva-54621 (URN)
Conference
16th ESCRH2022 Congress of the European Society of Contraception and Reproductive Health, Ghent, Belgium, May 25-28, 2022.
Projects
Experiences of involuntary childlessness during the Covid-19 pandemic
Funder
Interreg Öresund-Kattegat-Skagerrak
Available from: 2022-08-30 Created: 2022-08-30 Last updated: 2023-08-21Bibliographically approved
Hall, I. E., Holmström, C., Bodin, M., Schmidt, L., Ziebe, S. & Elmerstig, E. (2022). Experiences of involuntary childlessness during the COVID-19 pandemic. In: : . Paper presented at 5th ReproYoung Conference, Ystad, April 28-29, 2022..
Open this publication in new window or tab >>Experiences of involuntary childlessness during the COVID-19 pandemic
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2022 (English)Conference paper, Poster (with or without abstract) (Other academic)
Abstract [en]

BACKGROUND

The overall purpose is to investigate how the COVID-19 pandemic has affected individuals who have been or are going through assessment or treatment for involuntary childlessness, and their processes of trying to have children. Previous research on involuntary childlessness in relation to the pandemic has mainly been medical and quantitative, and there has been a lack of qualitative studies that explore the subject area on a more indepth level. The study is a project in ReproUnion, Challenge 5.

MATERIALS AND METHODS

In this qualitative study, we used semistructured interviews to collect data. The study includes individuals who have been or are going through assessment or treatment for involuntary childlessness in Sweden and Denmark during the pandemic. Participants were recruited from both public and private care. 26 individuals took part in the study, of which 18 women and eight men. The participants were between 24 53 years old and the sample consisted of both heterosexual and same sex couples. The interviews addressed experiences of assessment and treatment of involuntary childlessness during the COVID-19 pandemic in relation to e.g.access to care, socioeconomic factors and intimate relationships.

RESULTS AND CONCLUSION

The preliminary results show that the pandemic has affected the patients in many ways and made an already challenging process even more difficult.Obstacles mentioned are for example limit access to care with longer queues and uncertainty regarding when the treatment can be resumed. Many of the respondents has also suffered from the absence of partners during care visits. Furthermore, the fear of being infected by the Corona virus, which could cause the treatment to be postponed, has led to isolation and often a weaker support from family and friends. However, these negative consequences have affected patients to varying degrees, some worse than others. The results also show that the pandemic brought some positive consequences. For example, the isolation has been perceived as a relief for some as they easier could avoid being exposed to other people’s pregnancies as well as attending baptisms and baby showers.

“It has been extremely stressful for me to hear those messages [about delays of the treatment from the clinic], as it has taken so long to get started , and, yes, I am not getting any younger. That's how I feel. For every six months that goes by, I have kind of lost a chance to get pregnant.”

"We are young and have no underlying health problems, but we still really had to isolate ourselves, and we were very afraid that we would catch a cold or suffer from Corona so that the treatments would be cancelled. So, it was all the time that you were afraid to meet people, and you were afraid to meet your friends”

“I think the biggest impact was that I was not allowed to accompany and that I was not allowed to participate, also in combination with this stress that you could get sick. That was probably thebiggest impact for me and my wife.”

CONTACT

Ida Elisabet Hall

Research assistant, social worker, master in sexology

Centre for Sexology and Sexuality Studies, Malmö University

ida.hall@mau.se

 

National Category
Other Health Sciences
Identifiers
urn:nbn:se:mau:diva-53568 (URN)
Conference
5th ReproYoung Conference, Ystad, April 28-29, 2022.
Available from: 2022-06-27 Created: 2022-06-27 Last updated: 2023-08-21Bibliographically approved
Projects
Reflections on fertility and family planning in different stages of life; Malmö University
Organisations
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0003-2255-6547

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