The 37th session of the UN Human Rights Council took place from February 26 to March 23rd 2018.
The HRC37 Recap from the Sexual Rights Initiative (SRI) provides information on some of the key sexual rights related:
Resources to be listed in Resources section page(s)
The 37th session of the UN Human Rights Council took place from February 26 to March 23rd 2018.
The HRC37 Recap from the Sexual Rights Initiative (SRI) provides information on some of the key sexual rights related:
In June 2017, the United Nations Human Rights Committee ruled for the second time that by prohibiting and criminalizing abortion, Ireland violated a woman’s fundamental human rights. In the case of Whelan v. Ireland, the Committee held that by prohibiting Ms. Whelan from accessing abortion services in Ireland, the state subjected her to severe mental anguish and suffering. As a result, Ireland violated her rights to freedom from cruel, inhuman or degrading treatment, to privacy, and to equality before the law. This factsheet highlights the key aspects of this decision.
International technical guidance on sexuality education: An evidence-informed approach was published in 2018 by UNAIDS, UNFPA, UNICEF, UN Women, and the World Health Organization.
It is a revised edition of the 2009 guidance and benefits from a new review of the current evidence, and reaffirms the position of sexuality education within a framework of human rights and gender equality.
The International technical guidance on sexuality education was developed to assist education, health and other relevant authorities in the development and implementation of school-based and out-of-school comprehensive sexuality education programmes and materials. It is immediately relevant for government education ministers and their professional staff, including curriculum developers, school principals and teachers. Non-governmental organizations (NGOs), youth workers and young people can also use the document as an advocacy or accountability tool, for example by sharing it with decision-makers as a guide to best practices and/or for its integration within broader agendas, such as the SDGs. The Guidance is also useful for anyone involved in the design, delivery and evaluation of sexuality education programmes both in and out of school, including stakeholders working on quality education, sexual and reproductive health (SRH), adolescent health and/or gender equality, among other issues.
Gender is not an illness: How pathologization violates human rights law
This paper was conceived and produced by GATE as a contribution to the ongoing process of depathologizing trans and gender diverse people through the reform of classification systems, legal frameworks and social attitudes.
Pathologization appears to be a new concept in the human rights field; however, it describes the lived experiences of many trans and gender diverse people around the world over the last several decades. It conveys and executes a naturalized distinction between acceptable and unacceptable ways of being in the world –namely, “healthy” and “pathological”. Historically, those of us who identify ourselves in a gender different to the sex assigned to us at birth have faced stigma, discrimination and violence because being ourselves was considered to be, in itself, a pathology. Sadly, this history remains our shared present.
Pathologization has also been consistently used to deny, restrict and condition trans and gender diverse people’s access to very basic rights, including legal gender recognition, gender-affirming healthcare, and its coverage. Institutionalization, “conversion” treatments, mandatory psychotherapy, coercive surgeries, invasive mental and physical examinations, sterilization, and forced divorce are intrinsic parts of the requirements imposed upon us every time and place our gender is considered to be an illness.
As a critical framework, depathologization was created and established by those communities and movements primarily affected by its negative effects. In spite of our visibly marginalized situation in mainstream human rights spaces and the spread of epistemic injustice associated with being defined as “pathological” subjects, trans and gender diverse activists have been able to create the language to address the norms defining, oppressing and excluding us. After years of intense trans and gender diverse organizing, that language has been adopted by official institutions.
The main goal of this paper is to highlight how pathologization sits within the international human rights framework as a specific root for human rights violations, and as set of practices and consequences that extend those violations from childhood to adulthood. Moreover, the introduction of pathologization as a key human rights concern is a necessary step to dismantle its pervasive influence and to finally make depathologization a reality for all.
The paper was authored by Sheherezade Kara, with the contribution of an international group of experts: Amets Suess-Shwend, Cianán B. Russell, Viviane Vergueiro, Eleonora Lamm, Eszter Kismodi and Mauro Cabral Grinspan.
To celebrate the release of the YPplus10 and to highlight its relevance for our different communities, from today GATE is publishing a series of briefings related to different aspects of the document. Their first briefing focuses on intersex issues.
The Yogyakarta Principles[1] were first created in 2006, primarily at an expert meeting in Yogyakarta, Indonesia. The intention was (and remains) to apply international human rights law to sexual orientation and gender identity. The new 2017 Supplement extends the Principles to formally also include sex characteristics and gender expression.
There was only one intersex activist at the expert meeting in Yogyakarta: Mauro Cabral Grinspan. For the 2017 Supplement, Mauro (now of GATE) and Morgan Carpenter (OIIAU and GATE) were part of the drafting committee. Many other human rights and legal experts joined a new expert meeting in Geneva, in September 2017. Those participants came from all around the world, and from intersex, trans, LGBT, and other backgrounds; they included Kimberly Zieselman (interACT).
The original Principles mention intersex in the preamble, and make reference to a range of rights that benefit all people, including intersex people, on grounds of sexual orientation and gender identity. Principle 18B seeks to end human rights violations in medical settings. However, the language of the original Principles did not meet the aspirations of the intersex participant, and Principle 18B is constrained by the simplistic way it referenced the child’s best interests. In recent years, the UN has recognised that the concept of best interests can (and has been) manipulated,[2] and used to justify cruel or degrading treatment and violations of the right to bodily integrity.[3]
While widely cited in relation to the rights of people of diverse sexual orientation and (to a lesser extent) gender identity, the Principles have had even less impact in promoting the rights of intersex people.
Given the importance of the Principles in establishing the rights of people on grounds of sexual orientation and gender identity, we hope that the Supplement will promote the rights of all people on grounds of sex characteristics, and gender expression. The 2017 review aims to be feminist, intersectional, and fully reflect the needs of (overlapping) intersex and trans populations.
The Principles are a tool that people and organisations can use in advocacy. There is nothing obligatory about them, but we hope that they will encourage better recognition of intersex human rights issues by people who use a SOGI framework, and encourage adoption of SO/GIE/SC lenses.
The Supplement defines sex characteristics in this way:
UNDERSTANDING ‘sex characteristics’ as each person’s physical features relating to sex, including genitalia and other sexual and reproductive anatomy, chromosomes, hormones, and secondary physical features emerging from puberty;
This definition provides a powerful tool for the recognition of the rights of people in the context of changes to sex characteristics, and discrimination on the basis of sex characteristics. The term ‘sex characteristics’ is already used to define intersex and tackle violence and discrimination against intersex bodies. The term already appears in popular and widespread definitions of intersex, such as those produced by the UN:
Intersex people are born with physical or biological sex characteristics (such as sexual anatomy, reproductive organs, hormonal patterns and/or chromosomal patterns) that do not fit the typical definitions for male or female bodies. For some intersex people these traits are apparent at birth, while for others they emerge later in life, often at puberty.[4]
A definition of sex characteristics was also written into law in Malta in 2015, providing a first legislative protection for children from forced modifications to sex characteristics.
The definition of sex characteristics in the YP is universal – it applies to everyone, as everyone has some combination of sex characteristics, including both innate and acquired sex characteristics. Intersex characteristics are problematised prenatally, at birth and in childhood, adolescence and even adult life. Genital mutilation and trauma change sex characteristics. Not all changes are human rights violations: gender affirmation surgery also changes sex characteristics.
Legislative protection on grounds of sex characteristics can protect from human rights violations and it can also protect from discrimination.
The term does not require that people use the word ‘intersex’ to describe themselves. It is not associated with any specific legal sex classifications or gender identities. By encouraging specificity about what is meant by sex, ‘sex characteristics’ can promote better language about what it means to be born with an intersex variation, and our diversity.
The preamble defines sex characteristics. It also recognises the distinct needs, characteristics, and human rights situations of different populations on grounds of sexual orientation, gender identity, gender expression and sex characteristics. It recognises that the needs, characteristics and situations of intersex people thus differ from those of gay men. The preamble also recognises other intersectionalities, including due to racialisation, and Indigeneity.
This principle calls for an end to sex/gender registration and inclusion in legal identification documents. This is based upon International Covenant on Civil and Political Rights article 24 and Convention on the Rights of the Child article 7.[5] These articles call for the registration of children with a name and a right to acquire a nationality. This might seem radical, but the International Covenant on Civil and Political Rights was signed back in 1966 and neither the Covenant nor the Convention require registration of any ‘biological’ characteristics.
The Principles outlines interim measures while legal systems require sex/gender on identification documents, including simple administrative mechanisms to change classifications, and recognition of multiple gender markers.
This principle recognises that forced and coercive medical practices violate human rights principles on freedom from torture, cruel, inhuman and degrading treatment (a principle which includes freedom from experimental treatment). It also recognises that such practices violate to the right to bodily integrity, a right that derives from the right to personal security. The principle requires free prior and informed consent except in situations of urgent necessity for medical treatment. It calls on governments to combat the stigma and stereotypes that underpin treatment.
The Principles also seeks to manage problems with ‘best interests’ test, and calls for independent counselling.
This principles builds on rights established to combat impunity,[6] including an individual’s right to the truth about their medical history and access to redress, reparations and restorative treatments; to systemic rights to preserve memory and guarantee the right to know.[7] The Principle calls for this to not be subject to statutes of limitations.
The Principles already call for access to healthcare, including gender affirming healthcare. They also call for rights to protection from poverty (34), the right to sanitation (35) including access to toilet facilities, and the enjoyment of information and communication technologies.
A number of State Obligations have a direct and immediate relationship to the human rights situation of intersex people:
[1] Read the first Yogyakarta Principles and the YP+10 supplement at: http://yogyakartaprinciples.org
[2] Committee on the Rights of the Child. General Comment No. 14 (2013) on the right of the child to have his or her best interests taken as a primary consideration (art. 3, para. 1). 2013. Report No.: CRC/C/GC/14, para. 34. Available from: http://undocs.org/CRC/C/GC/14
[3] Committee on the Rights of the Child. General Comment 13: Article 19: The right of the child to freedom from all forms of violence. 2011. Report No.: CRC/C/GC/13, para. 54. Available from: http://undocs.org/CRC/C/GC/13
[4] Office of the High Commissioner for Human Rights, African Commission on Human and Peoples’ Rights, Council of Europe, Office of the Commissioner for Human Rights, Inter-American Commission on Human Rights, Special Rapporteur on torture and other cruel, inhuman, or degrading treatment or punishment, Special Rapporteur on the right of everyone to the enjoyment of the highest attainable standard of physical and mental health, et al. Intersex Awareness Day – Wednesday 26 October. End violence and harmful medical practices on intersex children and adults, UN and regional experts urge. 2016. Available from: http://www.ohchr.org/EN/NewsEvents/Pages/DisplayNews.aspx?NewsID=20739&LangID=E
[5] United Nations. International Covenant on Civil and Political Rights. 1966. Available from: http://www.ohchr.org/EN/ProfessionalInterest/Pages/CCPR.aspx; United Nations. Convention on the Rights of the Child. 1989. Available from: http://www.ohchr.org/Documents/ProfessionalInterest/crc.pdf
[6] Orentlicher D, Economic and Social Council. Report of the independent expert to update the Set of principles to combat impunity, Diane Orentlicher Addendum Updated Set of principles for the protection and promotion of human rights through action to combat impunity. UN Commission on Human Rights; 2005 Feb. Report No.: E/CN.4/2005/102/Add.1. Available from: http://undocs.org/E/CN.4/2005/102/Add.1
[7] World Conference against Racism, Racial Discrimination, Xenophobia and Related Intolerance. Durban Declaration and Programme of Action. 2001, para 98. Available from: http://www.un.org/WCAR/durban.pdf
[8] Toebes B. Sex selection under international human rights law. Medical Law International. 2008;9(3):197–225. Available from: http://www.rug.nl/research/portal/publications/sex-selection-under-international-human-rights-law(306b9838-c767-4c3b-9daf-c33be0168f24).html
[9] Ledford H. CRISPR fixes disease gene in viable human embryos. Nature News. 2017 Aug;548(7665):13. Available from: http://www.nature.com/news/crispr-fixes-disease-gene-in-viable-human-embryos-1.22382
The struggle for the rights of disabled persons have long been an arduous journey, fraught with pseudo-sciences and external factors such as conflict and poverty.
People with disabilities are often subjected to discrimination and violence, and to a large extent are deprived of their right to live independently. Within this struggle for human rights for disabled persons lie a subject that is rarely touched upon, that of their sexual and reproductive health and rights (SRHR), and it is at this juncture that this ARROW for Change bulletin positions itself. From looking at how disability is viewed through the lens of art pieces created by disabled artists, disabled women’s place in a society that places high regards in a woman’s reproductive capabilities in the context of marriage, to an interview that sheds light on the intersectionalities of mental disabilities and SRHR, the current bulletin seeks to fill in gaps in knowledge in the disability terrain.
A guide to rights-based messaging
This guide from IPPF is designed to help organizations review communications materials that include messages about abortion. It includes some basic information about abortion and related issues, and checklists to review and improve abortion messaging.
The guide includes chapters on:
This factsheet from Planned Parenthood demonstrates the many health benefits — physical, emotional, and social — that have resulted in the US since have 1973, when the U.S. Supreme Court legalized abortion in its decision, Roe v. Wade
In sum, no amount of controversy over abortion can negate the evidence that American women, men, children, and families have reaped great benefits to their physical, mental, and social health from the U.S. Supreme Court’s historic decision in Roe v. Wade. Any erosion of a woman’s right and access to medically safe, legal abortion jeopardizes the health of women, their families, and the nation as a whole.
Key points:
This six-page position paper from the Sexual Rights Initiative lays out the fundamental right to abortion from an international legal perspective.
The paper also outlines the unintended effects of criminalization: the denial of women’s fundamental rights to life, to health, to bodily autonomy, to freedom from torture, and to freedom from discrimination.
The final section discusses the two levels of discrimination that occur when abortion is made illegal. The first, embedded in the laws themselves, is sex discrimination: the laws criminalize health services used exclusively by women. The second level of discrimination is de facto: the criminalization of abortion disproportionately harms women in poverty, adolescent girls, women living in rural areas, and women who are members of other disadvantaged groups (migrants, ethnic minorities, etc.)
The so-called Alliance Defending Freedom (ADF) is one of the USA’s most dangerous organisations working to prevent equality for LGBT people.
An enthusiastic leader in defending the unconscionable “right” to discriminate against LGBT people, they are also a world-wide exporter of their own brand of hate. ADF bills itself as an “alliance-building legal organization that advocates for the right of people to freely live out their faith”—unless of course that faith contradicts with their own anti-LGBT version.
This paper presents 10 of the ways the ADF is supposedly working to protect their “freedom” to discriminate:
This profile was produced by the Human Rights Campaign.