Bodily autonomy in Malaysia: Perceptions and Experiences Across LGBTIQA and gender diverse life stages (18 – 55+)

Bodily autonomy in Malaysia: Perceptions and Experiences Across LGBTIQA and gender diverse life stages (18 – 55+)

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Resources
/Reports/
Bodily autonomy in Malaysia: Perceptions and Experiences Across LGBTIQA and gender diverse life stages (18 – 55+)
June 15, 2026

Sexual and reproductive health and rights (SRHR) encompass a broad range of issues related to physical, mental, and social well-being in relation to the reproductive system and its functions. This includes access to contraception; fertility and infertility care; maternal and perinatal health; prevention and treatment of sexually transmitted infections (STIs); protection from sexual and gender-based violence; and education on safe and healthy relationships.

For LGBTIQ and gender-diverse persons in Malaysia, the availability, accessibility, and affordability of these services are deeply shaped by the country’s socio-cultural and legal environment. The criminalisation, pathologisation, and stigmatisation of LGBTIQA and gender-diverse persons contribute to perceptions that they are “abnormal” and in need of “correction” Consequently, LGBTIQ persons may face not only exclusion from healthcare systems, but also harm arising from pathologising and medicalising practices that are institutionalised and legitimised within medical frameworks. These conditions also deter health-seeking behaviour.

This context, coupled with the increasingly conservative environment, further constrains the implementation of sex-positive, evidence and rights-based strategies.

Additionally, discriminatory legal frameworks further isolate LGBTIQA and gender-diverse people and leave them without adequate protection. This creates additional barriers to forming, maintaining, and securing legal recognition for their relationships and families.

Discrimination and marginalisation are also key social determinants of health, non-medical factors that influence health outcomes and quality of life. Their impact is evident among LGBTIQ populations. In Malaysia, the prevalence of mental health conditions among LGBTQ persons is reportedly twice that of the general population. Globally, UNAIDS reports that HIV prevalence is five times higher in countries that criminalise LGBTQ people compared to those that do not. In Malaysia, gay, bisexual, and queer (GBQ) men, as well as other men who have sex with men (MSM), are projected to be the populations most affected by HIV by 2030.

Access to sexual reproductive and health (SRH) services for LGBTIQ persons in Malaysia can be assessed across three categories, arranged by level of accessibility:

  1. General healthcare services, which LGBTIQ and gender-diverse persons access for routine medical needs and emergencies.
  2. HIV-related services, one of the most developed areas of SRH services in Malaysia, though primarily targeted at GBQ men and trans women.
  3. LGBTIQ-specific healthcare services, including gender-affirming care, assisted reproductive technologies, and specialised sexual health services. These remain the least developed and are primarily, though unevenly, available in the private sector. LGBTIQ-specific healthcare needs vary across different LGBTIQ populations.

This survey identifies the following key findings:

LGBTIQA and gender diverse persons’ access to healthcare services depends on the types of healthcare services sought. General healthcare services are relatively accessible; however, the quality of care is inconsistent. This is likely due to gaps in cultural competence, including the limited integration of gender-affirming practices within the general healthcare system. LGBTIQA-specific healthcare services remain the least accessible. 

There are significant gaps between the recognition of need and the receipt of appropriate care, particularly for LGBTIQA-specific services. A substantial proportion of participants were unable to access services despite identifying a need.

For example, only half of the 75 participants who required gender-affirming care were able to access it. Among 51 participants who had considered starting a family, only 17 felt comfortable discussing fertility plans with healthcare providers, and just five proceeded with those plans.

Gaps persist in access to HIV services beyond the commonly recognised key affected populations. Trans men, transmasculine persons and cisgender women reported barriers in accessing pre-exposure prophylaxis (PrEP) despite needing it.

Fear of discrimination, trust deficit and lack of knowledge on how to access support services were the most commonly reported barriers to accessing services and redress. Participants reported intersecting forms of discrimination, including ableism, racism, fatphobia, and discrimination based on body size.

Cost emerged as a significant barrier for participants in accessing SRH services, largely due to the fact that such services are primarily available in the private sector and not within the National Healthcare System (NHS). This was particularly evident among those seeking gender-affirming care, with 40% citing cost as a barrier. Participants also highlighted financial barriers in accessing safer sex tools, as some products are not readily available locally.

Between 78% and 90% of the 142 participants reported experiencing GBV across various settings (online, offline, and schools) over their lifetime. The findings indicate that participants’ experiences of GBV due to their SOGIESC often began in childhood and continued into adulthood. 28.2% (40 participants) reported experiencing GBV within the past 12 months. Cisgender queer women and transgender participants reported higher incidences of GBV. 

Sexual violence was among the most commonly reported forms of GBV. While it was experienced across the LGBTIQ spectrum, cisgender queer men reported relatively higher incidences compared to other groups.

Additionally, the survey also found multiple forms of GBV experienced by participants: 

  • 33.8% reported experiencing pressure to change their sexual orientation, gender identity and expression, or sex characteristics (SOGIESC).
  • 12% reported being forcibly subjected to therapy or institutionalisation in health facilities due to their SOGIESC.
  • 12%—mostly cisgender queer women—reported family pressure to marry or change their SOGIESC.
  • Three participants (two intersex and one transgender) reported non-consensual medical interventions.

Only 5% of the survey participants reported incidents of GBV, while 10% reported technology-facilitated gender-based violence (TFGBV). Similarly, only nine sought support services. Lack of knowledge on how to access support services was a common barrier. 

Additionally, the findings surfaced some patterns that warrant further interrogation, particularly in relation to perceptions of GBV and SRHR needs. 

  • Perception of GBV and discrimination 
    One of the most commonly cited reasons for not reporting GBV was participants’ perception or self-assessment that incidents were not “serious enough”. This raises important questions about both the severity of the incidents and participants’ understanding and recognition of discrimination.

  • Perception of need 
    Participants who reported not needing access to SRH services outnumbered those who reported needing access, raising questions about broader gaps in awareness, perceived relevance, and accessibility of sexual and reproductive healthcare services.

To that end, in addressing gaps in availability and access to SRHR and GBV safeguards, the report identifies several recommendations, categorised under four key pillars:  

  1. Create an enabling legal environment for LGBTIQA and gender-diverse persons 
  2. Strengthen a responsive and inclusive healthcare system
  3. Develop a survivor-centred and trauma-informed GBV response for LGBTIQ and gender-diverse persons 
  4. Promote a safer and more inclusive environment for LGBTIQ and gender-diverse students in schools