‘I never see anyone like myself represented in discussions about endometriosis’: priorities of LGBTQIA + endometriosis patients in New Zealand-Reference-Cited by-同舟云学术

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‘I never see anyone like myself represented in discussions about endometriosis’: priorities of LGBTQIA + endometriosis patients in New Zealand

Published:2024-08-28 Issue: Volume: Page:1-21
ISSN:1369-1058
Container-title:Culture, Health & Sexuality
language:en
Short-container-title:Culture, Health & Sexuality

Author:

Ellis Katherine¹²^ORCID,Armour Wayne³,Wood Rachael¹⁴^ORCID

Affiliation:

1. Department of Chemical and Process Engineering, University of Canterbury, Christchurch, New Zealand

2. Endometriosis New Zealand, Christchurch, New Zealand

3. NZBMA, Christchurch, New Zealand

4. Biomolecular Interaction Centre, University of Canterbury, Christchurch, New Zealand

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/13691058.2024.2394650

Reference57 articles.

1. AIHW. 2023. 1 in 7 Australian Women Aged 44–49 Have Endometriosis. Canberra: Australian Institute of Health and Welfare.

2. Endometriosis and chronic pelvic pain have similar impact on women, but time to diagnosis is decreasing: an Australian survey

3. The cost of illness and economic burden of endometriosis and chronic pelvic pain in Australia: A national online survey

4. Incidence and predictors of persistent pelvic pain following hysterectomy in women with chronic pelvic pain

5. Hormone Therapy, Mental Health, and Quality of Life Among Transgender People: A Systematic Review

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