Restraints and seclusion in schools by Erich Kofmel

On 4 April 2016, Autistic Minority International organized a World Autism Awareness Day side event and thematic briefing on "Autistic behaviours and the use of physical and mechanical restraints and seclusion in schools" for the expert members of the United Nations Committee on the Rights of Persons with Disabilities.

Our speakers were Briannon Lee and Michelle Sutton, co-conveners of the Autistic Family Collective (Australia), Riki Entz, chapter co-leader of the Autistic Self Advocacy Network (Canada), and Helena Stephenson, a survivor of restraint and seclusion in school and campaigner against their continued use in the United States.

Rationale: Education is not inclusive when students with disabilities, such as autistic children, are subjected to restrictive practices or aversive procedures/interventions, including physical, mechanical, and chemical restraint and seclusion/isolation, in special and regular schools alike, for the purpose of managing and modifying their behaviour and enforcing discipline and compliance. Children with disabilities are restrained by teachers and other school staff by being pinned to the floor, tied down to a chair, taped to the wall, and so on. Students may be locked into seclusion rooms, closets, or cages frequently and for lengthy periods of time, with no way of escape. Often they are unable to communicate the abuse, and parents will not be informed. Children have died, and post-traumatic stress is common in adult survivors.

From Erich Kofmel's opening and chairing remarks: "In 2013, your Committee noted in its Concluding Observations on Australia 'that persons with disabilities, particularly those with intellectual impairment or psychosocial disability, are subjected to unregulated behaviour modification or restrictive practices such as chemical, mechanical and physical restraints and seclusion, in various environments, including schools, mental health facilities and hospitals'. Unfortunately, the Committee then missed the opportunity to recommend a ban on restraints and seclusion in schools, and instead recommended the abolition of 'intrusive medical interventions' only, disregarding that restraints and seclusion in schools serve no medical purpose, but rather aim at managing and modifying students' behaviour and enforcing discipline and compliance.

"Autistic students are at a particular risk of becoming the victims of such abusive, degrading, and torturous restrictive practices or aversive procedures or interventions, be it in special or regular schools. With the General Comment on inclusive education, you now have an opportunity to rectify the previous omission and protect these children. We urge the Committee to add a paragraph to the General Comment rejecting the use of restraints and seclusion in schools. Our speakers today will tell you why. [...]

"There is no excuse for violence by teachers and school staff against students with disabilities.

"[In] the United States, [...] restraints and seclusion were used at least 267,000 times in the school year 2011-12. There were 163,000 instances of restraint and 104,000 of seclusion. In 75 percent of the cases, it was kids with disabilities who were restrained or secluded. In less than 7 percent of the incidents reported was the child considered 'violent'. Over 70 percent of the incidents reported the child as 'non-compliant' before the incident occurred. Many US students have died because of restraints and seclusion, such as Jonathon King, who had spent so much time in a seclusion room at his school that he had told them he was going to kill himself if they put him back in there. On Jonathon's final day, he was placed in seclusion because his pants were too big. The school gave him a rope to hold his pants up, but put him in the seclusion room regardless. Jonathon hung himself from the seclusion room door with the very rope the school gave him."

Unfortunately, the USA hasn't ratified the Convention on the Rights of Persons with Disabilities, which means that the CRPD Committee isn't able to comment on this practice there. But they are able to comment on its use in countries such as Australia, the UK, and Canada.

Subsequent to our side event, the Committee did indeed include a reference to restraints and seclusion in its General Comment No. 4 on the right to inclusive education, adopted in August 2016:

"51. Persons with disabilities, in particular women and girls with disabilities, can be disproportionately affected by violence and abuse, including physical and humiliating punishments by educational personnel, for example through the use of restraints and seclusion and bullying by others in and en route to school. To give effect to article 16 (2), States parties are required to take all appropriate measures to provide protection from and prevent all forms of exploitation, violence and abuse, including sexual violence, against persons with disabilities. Such measures must be age-, gender- and disability-sensitive. The Committee strongly endorses the recommendations of the Committee on the Rights of the Child, the Human Rights Committee and the Committee on Economic, Social and Cultural Rights that States parties prohibit all forms of corporal punishment and cruel, inhuman and degrading treatment in all settings, including schools, and ensure effective sanctions against perpetrators. It encourages schools and other educational centres to involve students, including students with disabilities, in the development of policies, including accessible protection mechanisms, to address disciplinary measures and bullying, including cyberbullying, which is increasingly recognized as a growing feature of the lives of students, in particular children."

The General Comment also includes two references (paragraphs 6 and 35 d-f) to autism and inclusive education. Unfortunately, most of the issues we raised from the autistic perspective during the consultation phase on this General Comment weren't addressed.

http://docstore.ohchr.org/SelfServices/FilesHandler.ashx?enc=6QkG1d%2fPPRiCAqhKb7yhsnbHatvuFkZ%2bt93Y3D%2baa2r7WiHwAXZ%2fG9E0uHt5DxBGZc%2fFYqJnjv7FqnztqhiHjL6HK2ahbb93gALzYRp%2fNPbB4kYh9RqO15ijXwSYDQWO

UN on consulting autistic persons by Erich Kofmel

The United Nations Committee on the Rights of Persons with Disabilities has adopted its General Comment No. 6 on equality and non-discrimination.

http://tbinternet.ohchr.org/Treaties/CRPD/Shared%20Documents/1_Global/CRPD_C_GC_6_8649_E.docx

It includes one reference to autistic persons:

"33. Regarding the consultation obligations of States parties, article 4 (3) and article 33 (3) of the Convention emphasize the important role that organizations of persons with disabilities must play in the implementation and monitoring of the Convention. States parties must ensure that they consult closely and actively involve such organizations which represent the vast diversity in society, including children, autistic persons, persons with a genetic or neurological condition, persons with rare and chronic diseases, persons with albinism, lesbian, gay, bisexual, transgender or intersex persons, indigenous peoples, rural communities, older persons, women, victims of armed conflicts and persons with an ethnic minority or migrant background. Only then can it be expected that all discrimination, including multiple and intersectional discrimination, will be tackled."

This is promising as the Committee currently is also working on a General Comment on articles 4 (3) and 33 (3) of the Convention on the Rights of Persons with Disabilities specifically, although it may need to be stressed further that States parties to the Convention must consult with autistic-led organizations (run by and for actually autistic persons), not just organizations of parents of autistic children.

Joint UN statement on autistic rights by Erich Kofmel

With World Autism Awareness Day (2 April) coming up once more, we would like to remind you of the joint statement on the human rights of autistic persons by the United Nations Special Rapporteur on the right to health and the Special Rapporteur on the rights of persons with disabilities for World Autism Awareness Day 2015. Autistic Minority International was asked to provide input for this statement, and we encourage you to use it during your own WAAD events and as an important advocacy tool all year round.

The joint statement is available in four of the six UN languages (English, Spanish, French, and Chinese, though not in Arabic or Russian):

English: http://www.ohchr.org/EN/NewsEvents/Pages/DisplayNews.aspx?NewsID=15787&LangID=E

Spanish: http://www.ohchr.org/FR/NewsEvents/Pages/DisplayNews.aspx?NewsID=15787&LangID=S

French: http://www.ohchr.org/FR/NewsEvents/Pages/DisplayNews.aspx?NewsID=15787&LangID=F

Chinese: http://www.ohchr.org/FR/NewsEvents/Pages/DisplayNews.aspx?NewsID=15787&LangID=C

Please also share the French, Spanish, and Chinese versions on any relevant fora or social media sites that use those languages.

"Discrimination against autistic persons, the rule rather than the exception – UN rights experts

"World Autism Awareness Day - Thursday 2 April 2015

"GENEVA (1st April 2015) – Two United Nations human rights experts today called for an end to discrimination against autistic persons and a celebration of diversity. Speaking ahead of World Autism Awareness Day, the Special Rapporteurs on the rights of persons with disabilities, Catalina Devandas Aguilar, and on the right to health, Dainius Puras, noted that about one per cent of the world's population - some 70 million people - is estimated to be on the autism spectrum worldwide.

"'As part of human diversity, autistic persons should be embraced, celebrated and respected. However, discrimination against autistic children and adults is more the rule rather than the exception.

"In many countries, autistic persons lack access to services which would support, on an equal basis with others, their right to health, education, employment, and living in the community. When available, services are too often far from human rights friendly or evidence-based.

"Autistic persons are particularly exposed to professional approaches and medical practices which are unacceptable from a human rights point of view. Such practices – justified many times as treatment or protection measures – violate their basic rights, undermine their dignity, and go against scientific evidence.

"Autistic children and adults face the proliferation of medicalized approaches relying on the over-prescription of psychotropic medications, their placement in psychiatric hospitals and long-term care institutions, the use of physical or chemical restraint, electro-impulsive therapy, etc. This may be particularly harmful and lead to the deterioration of their condition. All too often, such practices amount to ill-treatment or torture.

"The autism spectrum should be understood from a broader perspective, including in research. We call for caution about enthusiastic attempts to find the causes of autism and ways to 'cure' autism through sophisticated but not necessarily ethical research. Autism as a condition is a critical challenge for modern health systems, in which we need to ensure that the practice and science of medicine is never again used to cause the suffering of people.

"More investment is needed in services and research into removing societal barriers and misconceptions about autism. Autistics persons should be recognized as the main experts on autism and on their own needs, and funding should be allocated to peer-support projects run by and for autistic persons.

"It is about providing individuals and families with the necessary skills and support to have choice and control over their lives. It is also about equal opportunities, access to inclusive education and mainstream employment to achieve equality and rights enjoyment by autistic persons. It is about promoting their independence and respecting their dignity.

"Autistic persons should be respected, accepted and valued in our societies, and this can only be achieved by respecting, protecting and fulfilling their basic rights and freedoms.'

"Ms. Catalina Devandas Aguilar (Costa Rica) was designated as the first Special Rapporteur on the rights of persons with disabilities in December 2014 by the UN Human Rights Council. Ms. Devandas Aguilar has worked extensively on disability issues at the national, regional and international level with the Strategic Partnerships with the Disability Rights Advocacy Fund, the UN unit responsible for the Convention on the Rights of Persons with Disabilities and the World Bank. Her work has focused on the rights of women with disabilities and the rights of indigenous peoples with disabilities. Learn more, log on to: http://www.ohchr.org/EN/Issues/Disability/SRDisabilities/Pages/SRDisabilitiesIndex.aspx

"Mr. Dainius Pūras (Lithuania) was appointed as the Special Rapporteur on the right of everyone to the enjoyment of the highest attainable standard of physical and mental health by the UN Human Rights Council in June 2014. Mr Puras is a Professor and the Head of the Centre for Child psychiatry social pediatrics at Vilnius University. He is also a human rights advocate who has been actively involved during the last 30 years in the process of transforming public health policies and services, with special focus on the rights of children, persons with mental disabilities, and other vulnerable groups. Learn more, visit: http://www.ohchr.org/EN/Issues/Health/Pages/SRRightHealthIndex.aspx

"The UN Special Rapporteurs are part of what is known as the 'Special Procedures' of the Human Rights Council. Special Procedures, the largest body of independent experts in the UN Human Rights system, is the general name of the Council's independent fact-finding and monitoring mechanisms that address either specific country situations or thematic issues in all parts of the world. Special Procedures' experts work on a voluntary basis; they are not UN staff and do not receive a salary for their work. They are independent from any government or organization and serve in their individual capacity."

UN report on public decision-making by Erich Kofmel

If you haven't done so yet, we strongly encourage you to read the report by the United Nations Special Rapporteur on the rights of persons with disabilities, submitted to the March 2016 session of the UN Human Rights Council, on the participation of persons with disabilities in political and public life and decision-making.

It is available in all six UN languages (including English, French, Spanish, and Arabic) here:

http://ap.ohchr.org/documents/dpage_e.aspx?si=A/HRC/31/62

Autistic Minority International made a written submission during the consultation phase, and we are glad to note that there are a number of explicit references to autistic persons in the report:

"37. The Convention on the Rights of Persons with Disabilities has accelerated the process of establishing organizations of self-advocates with intellectual disabilities, of autistic persons and of other individuals who may need extensive support to express their positions. Organizations of parents and relatives of persons requiring support have often played a role in providing such support and one can find organizations that include parents as well as self-advocates. The role of parents in such organizations should increasingly move towards the provision of support, with self-advocates in full control.

"38. It is important to distinguish between organizations 'of' persons with disabilities, which are led by persons with disabilities, and organizations 'for' persons with disabilities, which are usually non-profit organizations that provide services to persons with disabilities and often also advocate on their behalf. This advocacy role needs to be carefully assessed, as it can easily happen that advocates seek to ensure the continuity of services, regardless of whether or not they are human rights-based or the preferred options of persons with disabilities. The failure of States to acknowledge the distinction between organizations 'of' and 'for' persons with disabilities lies at the heart of historical tensions between the two types of organization, such as those around legitimacy, choice and control, and the allocation of resources. In their pursuit of genuine participation by persons with disabilities in decision-making processes, States need to ensure that the will and preferences of persons with disabilities themselves are given priority. [...]

"60. States must promote the participation of persons with disabilities across all population groups, including those historically discriminated against or disadvantaged, such as indigenous people, poor or rural-based persons, lesbian, gay, bisexual, transgender and intersex persons, and others. States must also ensure that the voices of persons with disabilities from throughout the life cycle are heard (particularly those of children, adolescents and older persons) and from across the whole range of impairments and experiences of disability (including deaf persons, autistic persons, deafblind persons, and persons with psychosocial or intellectual disabilities). [...]

"69. As certain groups of persons with disabilities face additional challenges to their participation in public life, they may be inadequately represented by existing representative organizations in a given country. Accordingly, States must not only encourage and support the participation of persons with disabilities from disadvantaged groups in representative organizations of persons with disabilities, but also show flexibility and establish consultative mechanisms to enable the participation of all persons with disabilities. This is particularly important for persons with multiple impairments, persons with intellectual or psychosocial disabilities, autistic persons and deafblind persons. States must devise outreach strategies aimed at ensuring the participation of these groups. The broad inclusion of persons with disabilities throughout the public decision-making process is one of the most effective tools for States to develop truly inclusive and diverse societies."

In the press release accompanying the report, the Special Rapporteur highlighted the need for autistic self-advocacy organizations once more:

"In her report, Ms Devandas Aguilar urges all governments to engage in direct consultations with organizations of people with disabilities, rather than only those that advocate on their behalf. 'States must prioritize the participation of organizations led and operated by persons with disabilities and support their establishment and functioning,' she explained.

"The Special Rapporteur stressed the importance of engaging with groups who need considerable support, such as autistic people and those with intellectual or psychosocial disabilities."

http://www.ohchr.org/EN/NewsEvents/Pages/DisplayNews.aspx?NewsID=17147&LangID=E

Of course, pretty much everything in this report is relevant to the establishing and running of organizations by and for autistic persons and should be used by autistic self-advocates at all levels (local, national, regional, and global) to pressure governments for inclusion in decision-making processes, provision of funding to self-advocacy organizations, and so on.

Malta's autism acceptance law by Erich Kofmel

In May 2016, Malta became the first country to adopt an autism acceptance law, the "Persons within the Autism Spectrum (Empowerment) Act", passed by Parliament and subsequently enacted by the President and published in the Government Gazette. Autistic Minority International was consulted by the Maltese Government, through the good services of an autistic self-advocate from Malta, and was able to provide input on the draft bill earlier that year, including the suggestions to aim for autism acceptance, not just awareness, acknowledge the existence of undiagnosed adults on the autism spectrum, and promote research into ageing on the autism spectrum.

Provisions that may now serve as a model for similar legislation in other countries and jurisdictions include the mandate of the soon to be established Autism Advisory Council to "create awareness raising initiatives for the general public inter alia to achieve autism acceptance within society" and "focus on the need to improve identification of undiagnosed adults within the autism spectrum through a person-centre[d] diagnostic approach, addressing also the topic of autism and ageing", and to "give advice on [...] the promotion of self-determination of persons within the autism spectrum" as well as "the enhancement of access to appropriate support services and equal opportunities for inclusion and participation in society".

In addition, the Autism Advisory Council, which is to include at least one autistic adult, will aim "to empower persons within the autism spectrum by providing for their health, education, well-being and participation in all aspects of society and the betterment of their living conditions; [...] maximize the potential for children and adults within the autism spectrum through their personal autonomy and active citizenship; [...] and [...] identify the socio-economic, psycho-educational and health needs of persons within the autism spectrum with a view for Government to address these needs."

Also on the positive side, we note that the Act avoids speaking of "persons with autism" in favour of "persons within the autism spectrum". Unfortunately, the Act lacks strong provisions with regard to employment, due to domestic political considerations, and it places a misguided focus on early interventions, without paying attention to their potentially abusive nature and frequent disrespect for children's autistic identity.

An Autism Support State Plan and further regulations are to set out the details.

Autism, ageing, and premature death by Erich Kofmel

7 April is World Health Day. In 2017, the World Health Organization (WHO) decided to dedicate that day to "Depression". To commemorate both the United Nations' World Autism Awareness Day (2 April) as well as World Health Day, Autistic Minority International organized a public side event/thematic briefing for the members of the UN Committee on the Rights of Persons with Disabilities on Monday, 3 April 2017, 1.45-2.45 pm, at Palais des Nations, the European headquarters of the UN, in Geneva, Switzerland.

Theme: "Ageing and Premature Death on the Autism Spectrum"

Speakers: Wenn Lawson, psychologist, researcher, lecturer (Australia), Cos Michael, autistic autism consultant (United Kingdom), Alanna Rose Whitney, Autistic Acceptance Activism Alliance (Canada). Chair: Erich Kofmel, President, Autistic Minority International.

This was our fourth annual side event held during the spring session of the Committee mandated to monitor the implementation of the UN Convention on the Rights of Persons with Disabilities (CRPD) in all 177 countries that have ratified it. To the best of our knowledge our event was once more the only commemoration of World Autism Awareness Day at the United Nations in Geneva. All other related UN-based activities were concentrated in New York, even though major decisions with regard to autistic children and adults are made in Geneva, both in the human rights mechanisms and at the WHO. We therefore believe that it is important that actually autistic persons show presence here as well, on this our day.

According to the WHO, depression is the leading cause of disability worldwide. More than 300 million people are living with depression, and even in high-income countries 50% of people with depression do not get treatment. Depression is an important risk factor for suicide, which claims over eight hundred thousand lives each year, 75% of them in low- and middle-income countries. Every 40 seconds someone dies by suicide. It is the second leading cause of death among 15-29-year-olds. There are more deaths from suicide than from war and homicide together.

Many autistic persons never reach old age, falling victim to depression and suicide much earlier in their lives. We believe that depression and suicide in our community are the direct result of unmet needs and a lack of acceptance of autism. Suicide should be seen as a response to a society that is not accepting of autistic persons at all. As autistic self-advocates we believe that autism is not a disorder that needs to be cured or should be stigmatized, but a lifelong neurological difference that is equally valid.

Our previous side events were concerned with moving from autism awareness to autism acceptance (2014), the worldwide pain and sorrow caused by medical experimentation on autistic children (2015), and the devaluing of autistic behaviours and the use of physical and mechanical restraint and seclusion in schools (2016). These themes echoed throughout 2017's presentations. All the experiences we previously laid out before the Committee contribute to a sense of doom and futility that causes depression and suicidal ideation in autistic individuals.

Even though the speakers last year hailed from western countries, autistic persons are one percent of the population in any given country, albeit many of us remain undiagnosed or misdiagnosed due to a shortage of medical professionals qualified to diagnose autism in less developed countries. Many of us are counted for in suicide statistics the world over, without our deaths ever being linked to autism or the societal attitudes and barriers we faced and weren't able to overcome. Ours is an often hidden disability, and our deaths are hidden also.

No other age group illustrates the pressures exercised on us to hide and pretend to be "normal" as much as that of older persons on the autism spectrum, who are nearly invisible. With Asperger syndrome in particular not being diagnosed before the mid-1990s, most autistic adults, who in their majority are not intellectually disabled, never received a diagnosis as a child. Many previously undiagnosed or misdiagnosed adults now finally get an autism diagnosis, often subsequent to a child or grandchild being diagnosed as being on the autism spectrum. Regardless, little attention is paid to autistic adults and even less to elderly autistic persons. When talking about autism, most people still only think of children.

In many countries, support and services for autistic persons end when they reach adulthood. Families are growing increasingly concerned about what will happen to their children and dependent autistic adults when they are not able to take care of them anymore. Autistic adults may age prematurely, and research found that on average we die decades earlier than non-autistic persons, whether from suicide, frequent co-morbid health conditions and a lack of access to autism-appropriate health care, filicide (by relatives) or homicide (by caregivers).

Our side event and thematic briefing therefore sought to address health risks, premature mortality, ageing, and the rights of older persons on the autism spectrum from the perspective of the CRPD. All the examples presented from any one country were equally applicable to all other countries, in their respective context. The geographic origins of our speakers were not meant as a show of disrespect for other cultures and socio-economic situations, but owed to the uneven distribution of awareness of and knowledge about autistic adults and ageing on the autism spectrum.

It may seem frivolous also to talk about premature mortality in the autistic population when viewed from the perspective of countries with a much lower life expectancy in general, for persons with or without disabilities alike, but ultimately the right to life guaranteed by the CRPD applies to all, in all contexts, and any circumstances unduly shortening the life of persons with disabilities anywhere equally demand our urgent attention.

Autism in adulthood and old age may be hidden in most parts of the world, and our deaths may only be counted in suicide statistics, but those children everywhere diagnosed as part of the so-called autism "epidemic" will soon grow up and grow old and join us in demanding autism acceptance and an end to stigma and prejudice against autistic people. Many of us will be consumed by the fight for equality and succumb to depression, but others will take our place and fight on. We may die as individuals, but the worldwide autistic community will only grow stronger with age.

(Speakers' presentations are available upon request.)

Updated WHO factsheet on autism by Erich Kofmel

In April 2017, the World Health Organization (WHO) updated its factsheet on autism spectrum disorders that is supposed to provide key facts, data, and information on epidemiology, assessment, and management, social and economic impacts, as well as other related resources. While speaking of the human rights of autistic persons, they continue to undermine our human rights by using stigmatizing language such as "disorder" and "burden" and recommending early intervention and behavioural treatment (i.e. normalization, Applied Behaviour Analysis/ABA). The parent skills training programme they mention repeatedly was developed in collaboration with controversial US charity Autism Speaks, but without any input from actually autistic people.

http://www.who.int/mediacentre/factsheets/autism-spectrum-disorders/en/

Autism in UN report on mental health by Erich Kofmel

The United Nations Special Rapporteur on the right to health dedicated his 2017 report to the UN Human Rights Council to mental health. It includes a number of explicit mentions of autism and autistic persons.

"4. [...] Some have cognitive, intellectual and psychosocial disabilities, or are persons with autism who, regardless of self-identification or diagnosis, face barriers in the exercise of their rights on the basis of a real or perceived impairment and are therefore disproportionately exposed to human rights violations in mental health settings. Many may have a diagnosis related to mental health or identify with the term, while others may choose to identify themselves in other ways, including as survivors. [...]

"8. For decades, mental health services have been governed by a reductionist biomedical paradigm that has contributed to the exclusion, neglect, coercion and abuse of people with intellectual, cognitive and psychosocial disabilities, persons with autism and those who deviate from prevailing cultural, social and political norms. Notably, the political abuse of psychiatry remains an issue of serious concern. While mental health services are starved of resources, any scaled-up investment must be shaped by the experiences of the past to ensure that history does not repeat itself. [...]

"55. Adequate mental health services must be made available. In many countries, the limited mental health and social care available is based on a narrow biomedical model and institutionalization. [...] Services must support the rights of people with intellectual, cognitive and psychosocial disabilities and with autism to live independently and be included in the community, rather than being segregated in inappropriate care facilities. [...]

"58. Mental health services [...] must be culturally appropriate and acceptable to persons with intellectual, cognitive or psychosocial disabilities and with autism, adolescents, women, older persons, indigenous persons, minorities, refugees and migrants, and lesbian, gay, bisexual, transgender and intersex persons. Many within those populations are needlessly medicalized and suffer from coercive practices, based on inappropriate and harmful gender stereotypes. [...]

"62. In particular, children and adults with intellectual disabilities and with autism too often suffer from institutionalized approaches and excessively medicalized practices. Institutionalizing and medicating children with autism, based on their impairment, is unacceptable. Autism represents a critical challenge to modern systems of care and support, as medical attempts to 'cure' the condition have often turned out to be harmful, leading to further mental health deterioration of children and adults with the condition. Support for them should not only address their right to health, but their rights to education, employment and living in the community on an equal basis with others. [...]

"91. The Special Rapporteur calls for leadership to confront the global burden of obstacles and embed rights-based mental health innovation in public policy. That includes State champions in international policy efforts, the leadership of professional psychiatry in assessing constructively its approach to the necessity for change, managers of mental health services leading change by example and municipal officials championing grassroots innovation. These champions must work in partnership with their constituents, including persons with intellectual, cognitive and psychosocial disabilities and with autism."

Full text of the report in English:

https://documents-dds-ny.un.org/doc/UNDOC/GEN/G17/076/04/PDF/G1707604.pdf?OpenElement

Also available in French, Spanish, Arabic, Russian, and Chinese:

http://ap.ohchr.org/documents/dpage_e.aspx?si=A/HRC/35/21

Unfortunately, in a number of other places where autism should have been mentioned explicitly, it isn't (most importantly, with regard to legislation depriving people of legal capacity). Still, we feel that the mentions of autism are informed by discussions and interactions Autistic Minority International has had with the Special Rapporteur, and autistic self-advocates and allies should be using this report in our ongoing advocacy with the UN and national, regional and local governments.