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State Abuse Survivors aotearoa New Zealand

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Recommendation 2 - Apologies in Detail

Additional Information

The Prime Minister should make a national apology for historical abuse

and neglect in the care of the State (both direct and indirectly) in the

House of Representatives. 

The national apology should:

  1. be developed and agreed with a representative group of survivors
  2.  be consistent with the puretumu torowhānui system and scheme and the Recommendations from the Inquiry’s interim report, He Purapura Ora, he Māra Tipu: From Redress to Puretumu Torowhānui (2021)
  3. apologise to all survivors of abuse and neglect in State‑based care (both direct and indirect care), and include specific apologies to:
    1. the many who suffered abuse and neglect that have died and are no longer able to share their experiences and acknowledge them and their whānau, hapū, iwi, communities and support networks
    2. Māori survivors, their whānau, hapū, iwi, communities and support networks
    3. Pacific survivors, their kainga (family), communities and support networks
    4. Deaf survivors, their whānau, hapū, iwi, communities and support networks
    5. Disabled survivors, their whānau, hapū, iwi, communities and support networks
    6. Pākehā / NZ European survivors, their family, communities and support networks
    7. survivors who experienced mental distress, their whānau, hapū, iwi, communities and support networks
    8. Takatāpui, Rainbow, MVPFAFF+ survivors, their whānau, hapū, iwi, communities and support networks
  4. as outlined in He Purapura Ora, he Māra Tipu: From Redress to Puretumu Torowhānui (2021), make a specific apology to groups who were harmed, including Māori, where appropriate.

Recommendation 3 in Detail

Additional Information


Public acknowledgments and apologies for historical abuse and neglect in the care of the State (both direct and indirectly provided care) and faith‑based institutions should be made to survivors, their whānau and support networks by:

  1. a. the most senior leaders of all faith‑based institutions and in particular, and without limitation:
    1. the Pope should make a public apology and acknowledgement for the abuse and neglect in the care of the Catholic Church in Aotearoa New Zealand
    2. the Archbishop of Canterbury should make a public apology and acknowledgement for the abuse and neglect in the care of the Anglican Church in Aotearoa New Zealand and Polynesia
    3. the President Elect should make a public apology and acknowledgement for the abuse and neglect in the care of the Methodist Church in Aotearoa New Zealand
      1. the Moderator of the Presbyterian Church of AotearoaNew Zealand should make a public apology and acknowledgement for the abuse and neglect in the care of the Presbyterian Church of New Zealand
    4. the Chief Executive Officer (or equivalent) of each individual Presbyterian Support  Organisation should make public apologies and acknowledgements for abuse and neglect in the care of their respective Presbyterian Support organisation
    5. the General of The Salvation Army should make a public apology and acknowledgement for the abuse and neglect in the careof The Salvation Army of New Zealand, Fiji, Tonga and Samoa Territory
      1. the Overseeing Shepherd should make a public apology andacknowledgement for the abuse and neglect in the care of Gloriavale Christian Community
    6. the Governing Body of Jehovah’s Witnesses should make a public apology and acknowledgement for the abuse and neglect in the care of Jehovah’s Witnesses in New Zealand.
    7. public sector leaders, including the Public Service Commissioner, Solicitor‑General, Commissioner of NZ Police and the Chief Executives of Oranga Tamariki, the Ministry of Social Development, the Ministry of Health, and the Ministry of Education
    8. the leaders of relevant professional bodies, including the Royal Australian and New Zealand College of Psychiatrists, Medical Council of New Zealand, Aotearoa New Zealand Association of Social Workers, New Zealand Nurses Association, Teaching Council of Aotearoa New Zealand
    9. the leaders of all direct and indirect care providers, including Blind Low Vision NZ and IHC.
  2. Each public apology should be:
    1. developed and agreed with a representative group of survivors
    2. be consistent with the puretumu torowhānui system and scheme and the Holistic Redress Recommendations from the Inquiry’s interim report, He Purapura Ora, he Māra Tipu: From Redress to Puretumu Torowhānui

recommendation 15 in Detail

Additional Information

The government should ensure that the puretumu torowhānui system and scheme is designed and operated in a manner consistent with: 

  1. upholding the rights of Māori as indigenous peoples of Aotearoa New Zealand in accordance with United Nations Declaration on the Rights of Indigenous Peoples
  2. upholding the rights of Māori, Pacific Peoples, and people from other linguistically or culturally diverse backgrounds, in accordance with the Convention on the Elimination of all forms of Racial Discrimination
  3. upholding the rights of girls and women, in accordance with the Convention on the Elimination of All Forms of Discrimination against Women
  4. upholding the rights of Deaf, disabled people, and people who experience mental distress, in accordance with the Convention on the Rights of Persons with Disabilities and the Enabling Good Lives principles, including: 
    1. recognition that Deaf, disabled people, and people who experience mental distress in care have:
      1.  the same rights as others to make decisions that affect them, including adults having decision-making supports as appropriate
      2. the right to access and use supports (including communication assistance) in making and participating in decisions that affect them, communicating their will and preferences, and developing their decision-making ability
      3. access and use advocacy services in making and participating in decisions, and communicating their will and preferences
    2. that tāngata Turi, tāngata whaikaha and tāngata whaiora Māori and Pacific survivors who are Deaf, disabled, or experience mental distress, survivors from other culturally or linguistically diverse backgrounds, and Takatāpui, Rainbow and MVPFAFF+ survivors may experience barriers to engaging with the system and scheme due to cultural, language and other differences, and that these barriers need to be addressed. 
  5. upholding the rights of children, and ensuring that all parties involved in the design and operation of the system and scheme :
    1. act with the best interests of the child as a primary consideration, consistent with the United Nations Convention on the Rights of the Child
    2. recognise the rights of iwi, hapū and whānau Māori to retain shared responsibility for the wellbeing of tamariki and rangatahi Māori, consistent with the United Nations Declaration on the Rights of Indigenous Peoples.

recommendation 22 in Detail

Additional Information

The Solicitor‑General should: 

  1. amend the suite of prosecution guidelines to include a requirement that those making decisions about whether to prosecute, and which charges to file, act consistently with New Zealand’s international human rights obligations and other relevant international law obligations (including the United Nations Convention on the Rights of Persons with Disabilities, the United Nations Convention on the Rights of the Child and the United Nations Declaration on the Rights of Indigenous Peoples).
  2. amend the suite of prosecution guidelines to include, in relation to the evidential test for prosecution, a requirement that those making assessments on the credibility and quality of a complainant’s evidence recognise the potential for their own bias, obtain relevant expert advice where necessary, and provide appropriate accommodations where necessary.
  3. amend the suite of prosecution guidelines to include, as a public interest consideration for prosecution, that the offence was committed against a person in the care of the State or a faith‑based institution
  4. amend the suite of prosecution guidelines to strengthen obligations to engage appropriately (that is, more than consult) with complainants (including the use of communication assistance) on prosecution decisions, including when considering whether to prosecute because of the likely detrimental effect on a witness’s physical or mental health.
  5. amend the suite of prosecution guidelines to establish a review process for complainants who allege offences falling under Parts 7 or 8 of the Crimes Act 1961 where a decision has been made not to prosecute by NZ Police or a Crown Solicitor, which:
    1. is designed to ensure fairness and consistency in approach to charging decisions nationwide
    2. requires an evaluative review of the evidence and the decision not to prosecute. 
    3. establishes national panels of suitably trained and experienced prosecutors to conduct reviews of decisions not to prosecute made by NZ Police and Crown Solicitors.
    4. includes a requirement for the panel reviewing NZ Police decisions not to prosecute to seek legal advice from a Crown Solicitor where the decision is finely balanced and / or complex, or is an offence listed in the schedule to the Crown Prosecution Regulations 2013.
    5. has the power to refer a decision not to prosecute back to the decision maker for further consideration and / or investigation.
    6. ensures complainants are consulted in person with necessary accommodations.

recommendation 40 in Detail

National Care Safe Strategy

A new comprehensive National Care Safety Strategy, required by law, on the prevention of and response to abuse and neglect in care should include: 

  1. goals, objectives and targets that consider future generations.
  2. clearly understood roles and responsibilities for different organisations and entities involved in the care system.
  3. an overview of the priority programmes of work, including: 
    1. supporting and empowering victims, survivors, whānau. 
    2. strategies to prevent abuse and neglect. 
    3. better abuser accountability and intervention.
    4. improving the evidence base.
    5. awareness raising and education.
    6. enhancing approaches to children, young people, and adults in care with harmful sexual behaviours.

recommendation 41 in Detail

Establishing an independent Care Safe Agency

The government should establish a new standalone Care Safe Agency, with an independent Board to oversee it. The Care Safe Agency should be tasked with functions that include:

  1.  whole of system leadership on preventing and responding to abuse and neglect in care
  2. promoting and championing the Care Safety Principles (Recommendation 39)
  3. leading development and implementation of a National Care Safety Strategy and a supporting action plan to prevent and respond to abuse and neglect in care (Recommendation 40)
  4. setting care safety rules and standards (legislative and non- legislative) (Recommendation 47)
  5. monitoring and investigating compliance with the care safety rules and standards (Recommendation 47)
  6. enforcing penalties and sanction for breaches of the care safety rules and standards (Recommendation 47)
  7. developing best practice guidelines on care safety and preventing and responding to abuse and neglect in care
  8. investigating and reporting on complaints received directly from users of supports and services
  9. collating and keeping a centralised database of issues of concern, complaints, and the outcomes of investigations from all State and faith-based entities that provide care directly or indirectly to children, young people and adults in care, from professional registration bodies, and from independent oversight and monitoring entities (Recommendations 67–68)
  10. accrediting all State and faith-based entities providing care directly or indirectly to children, young people, and adults in care (Recommendation 48)
  11. registering staff and care workers who are not already covered by existing professional registration regimes (Recommendation 57)
  12. promoting a continuous improvement and learning culture in the care system, including facilitating regular forums and communities of practice and evaluation
  13. setting training and education standards and developing curriculums for staff and care workers
  14. workforce development and developing career pathways for staff and care workers (Recommendation 61)
  15. leading public awareness, education, and prevention initiatives (Recommendations 111–112 and 121–122)
  16. undertaking research, data analysis and horizon-scanning, including building evidence on the risk, extent and impact of abuse and neglect in care
  17. publishing data and statistics on complaints of abuse and neglect in care to promote transparency and measurability of outcomes
  18. advising government on preventing and responding to abuse and neglect in care, including where systemic deficiencies are identified.

In defining the scope and functions of the independent Care Safe Agency, the government should consider the additional points made in Chapter 3 of Part 9.

recommendation 54 in Detail

Creating a Culture of Safeguarding

The senior leaders of all State and faith‑based entities providing care directly or indirectly to children, young people and adults should take active steps to create a positive safeguarding culture, including by: 

  1. designating a safeguarding lead with sufficient seniority.
  2. supporting the prevention, identification and disclosure of abuse and neglect.
  3. ensuring the entity providing care directly or indirectly complies with its health and safety obligations.
  4. protecting whistleblowers and those who make good‑faith notifications.
  5. ensuring accountability for those who fail to comply with safeguarding obligations. 
  6. prioritising and supporting training and professional development in safeguarding and in abuse and neglect in care including the topics set out in Recommendation 63.
  7. actively promoting a culture that values all children, young people and adults in care and addresses all forms of discrimination.
  8. ensuring there are sufficient resources for safeguarding. 
  9. identifying and correcting harmful attitudes and beliefs, such as the disbelief or mistrust of complainants or racist or ableist actions and beliefs.
  10. ensuring there is adequate data collection and information on abuse and neglect in care, including relevant data on ethnicity and disability, to allow analysis and reporting.
  11. learning from any incidents and allegations.

recommendation 55 in Detail

Safeguarding Policies

All State and faith‑based entities providing care directly or indirectly should have safeguarding policies and procedures in place that:

  1. are consistent with the Care Safety Principles (Recommendation 39). 
  2. are consistent with the National Care Safety Strategy (Recommendation 40.
  3. are compliant with care safety rules and standards (Recommendation 47).
  4. re consistent with best practice guidelines issued by the Care Safe Agency.
  5. are tailored to the risks of the particular organisation and care provided.
  6. are clearly written.
  7. are published in a readily accessible format.
  8. give effect to te Tiriti o Waitangi.
  9. are culturally and linguistically appropriate.
  10. are responsive to the needs of children, young people and adults in care, including Māori, Pacific Peoples, Deaf, disabled people, people experiencing mental distress, and Takatāpui, Rainbow and MVPFAFF+ people.
  11. are regularly reviewed, including periodic external reviews.
  12. are audited for compliance, including periodic external audits.

recommendation 61 in Detail

Care Sector Workforce Strategy

The Care Safe Agency should develop a workforce strategy for the care sector that includes:

  1. ensuring there are enough people with the right skills, experiences and values to meet the needs of people in care including developing strategies to address skill gaps.
  2. identifying training needs.
  3. fostering positive workplace cultures where people in care and staff and care workers are valued and have their voices heard.
  4. strengthening support, supervision and management practices.
  5. improving workplace conditions including wellbeing, safe ratios workloads and remuneration.
  6. removing barriers to enter into the care workforce in a safe manner.
  7. ensuring opportunities for professional development and career progression, including:
    1. targeted measures to support career pathways for people with lived experience of care.
    2. targeted measures to support career pathways for Māori, Pacific Peoples, Deaf, disabled people, people who experience mental distress, and Takatāpui, Rainbow and MVPFAFF+ people.
  8. measuring staff and carer wellbeing and satisfaction.

recommendation 65 in Detail

Complaints are Responded to effectively

All State and faith‑based entities providing care directly or indirectly to children, young people and adults in care and relevant professional registration bodies should ensure they have appropriate policies and procedures in place to respond in a proportionate way to complaints, disclosures or incidents of abuse and neglect, including:

  1. the policies and procedures are guided by the Care Safety Principles (Recommendation 39) and any relevant rules, standards or guidelines issued by the Care Safe Agency (Recommendation 41).
  2. the policies and procedures are clearly written, accessible to people in care, 
  3. the policies, at a minimum, outline roles and responsibilities, how different types of complaints will be handled, including potential employment outcomes and reporting obligations.
  4. the policies set out how actual or perceived conflicts of interest will be addressed if they arise.
  5. there are clear protections in place for whistleblowers and those making good faith notifications.
  6. it is as easy as possible for people to make disclosures or complaints
  7. complaints processes are appropriate for Māori, Pacific People, Deaf, disabled people, people who experience mental distress and Takatāpui, Rainbow and MVPFAFF+ people including ensuring there is access to appropriate support.
  8. complainants are supported and kept informed throughout the handling of their complaint, including with the assistance of their independent advocates (Recommendation 76) if applicable.
  9. Complainants are kept safe throughout the handling of their complaint, including if they have complained about another person in care or a person who directly provides them care.
  10. Complaints are responded to promptly and robustly, including: 
    1. as soon as a complaint is made, carrying out an initial risk assessment to identify the risks to the complainant and to other children, young people and adults in care.
    2. mitigating identified risks while the complaint is being investigated, proportionate to the seriousness of the allegation.
    3. continuing to investigate and report on complaints even if the subject of the complaint voluntarily leaves employment and / or cancels their professional registration.
    4. carrying out a robust investigation at a level proportionate to the seriousness of the complaint.
    5. applying a standard of proof consistent with civil law (“on the balance of probabilities”) when investigating complaints, but doing so flexibly, proportionate to the seriousness of the allegation.
    6. using external investigators where appropriate for the most serious allegations.
    7. meeting all privacy and employment law obligations.
    8. ensuring appropriate accountability, including through reporting to NZ Police and relevant professional registration bodies if the complaint is substantiated (Recommendation 66).
  11. all complaints must be reported to the Care Safety Agency (Recommendation 41), regardless of the outcome of the investigation.
  12. each complaint must be reviewed for lessons identified and possible improvements.
  13. publicly report annually on how many complaints they are dealing with, whether they have been resolved, whether they have been substantiated, and how long the complaint took to be resolved.

recommendation 75 in Detail

Review Design Features of any institutional setting

All State and faith‑based entities providing direct or indirect care to children, young people and adults should review physical building and design features to identify and address elements that may place children, young people and adults in care at risk of abuse and neglect. This should include: 

  1. consideration of how best to use technology such as CCTV cameras and body cameras without unduly infringing personal privacy, including taking into account any applicable guidance documents and the legal requirements for the collection of personal information under the Privacy Act 2020.
  2. reviewing any policies or processes that place children, young people, or adults in care with others who may put them at risk (for example children and young people in care and protection being placed together with children, young people, or adults in the justice system).
  3. if care settings include physically isolated spaces, for example private offices or a confessional box, ensuring there are tailored measures in place to address the risks arising, including the risk of undetected abuse and neglect.
  4. if care is to be delivered in a geographically isolated or remote area, ensuring there are tailored measures in place to address the risks arising from the geographical setting, including the risk of undetected abuse and neglect.

recommendation 76 in Detail

Independent advocacy

The government should: 

  1. provide sufficient investment to enable children, young people, and adults in care to have access to an independent advocate of their choosing to support them to understand and exercise their rights, specifically: 
    1. each child, young person and adult in care and protection, youth justice, disability and mental health settings should have access to an individual independent advocate.
    2. children and young people in State, State-integrated and private schools should have access to at least one independent advocate per school.
  2. provide that independent advocates: 
    1. have appropriate communication skills (including for Deaf and disabled people in care).
    2. be independent from the care provider, and staff and care workers.
    3. be independent from their direct and immediate whānau of the person in care.
    4. proactively and regularly engage with the person in care, be available to respond in times of need, support the person in care when they need to raise issues with their carer, advocate for the right conditions, and / or generally provide peer support.
    5. have no power over the individual.
  3. provide that advocates are subject to the same regulatory standards and safeguards, including vetting, registration and training as other staff and care workers.

recommendation 81 n Detail

Best Practice data collection, record keeping and information sharing

All State and faith‑based entities directly or indirectly providing care to children, young people, Deaf, disabled people, and people who experience mental distress should adopt and comply with best practice guidelines for record keeping and data sovereignty, including the following principles: 

  1. Record‑keeping Principle 1: To create and keep full and accurate records. Creating and keeping full and accurate records relevant to safety and wellbeing is in the best interests of children, young people or adults in care and should be an integral part of institutional leadership, governance, and culture. Institutions that care for or provide services to children, young people or adults in care must keep the best interests of the child uppermost in all aspects of their conduct, including record keeping. It is in the best interest of children, young people, or adults in care that institutions foster a culture in which the creation and management of accurate records are integral parts of the institution’s operations and governance.
  2. Record‑keeping Principle 2: Records to include all incidents and responses. Full and accurate records should be created about all incidents, responses and decisions affecting the safety and wellbeing, including abuse and neglect in care, of children, young people, or adults in care. Institutions should ensure that records are created to document any identified incidents of grooming, inappropriate behaviour (including breaches of institutional codes of conduct) or abuse and neglect in care, and all responses to such incidents. Records created by institutions should be clear, objective, and thorough. They should be created at, or as close as possible to, the time the incidents occurred, and clearly show the author (whether individual or institutional) and the date created.
  3. Record‑keeping Principle 3: Records to be maintained in an indexed, logical and secure manner. Records relevant to the safety and wellbeing of children, young people or adults in care, including abuse and neglect in care, should be maintained appropriately and in an indexed, logical and secure manner. Associated records should be co-located or cross- referenced to ensure that people using those records are aware of all relevant information.
  4. Record‑keeping Principle 4: Records only be disposed of in accordance with law or policy. Records relevant to the safety and wellbeing, including abuse and neglect in care, of children, young people or adults in care should only be disposed of in accordance with law or policy. Records relevant to the safety and wellbeing, including abuse and neglect in care, of children, young people or adults in care must only be destroyed in accordance with records disposal schedules or published institutional policies. Records relevant to abuse and neglect in care should be subject to minimum retention periods that allow for delayed disclosure of abuse and neglect by victims and survivors and take account of limitation periods for civil actions for abuse and neglect in care.
  5. Record-keeping Principle 5: Individuals’ rights to access, amend or annotate records about themselves to be recognised to the fullest extent.
  6. Individuals’ existing rights to access, amend or annotate records about themselves should be recognised to the fullest extent including in a way that is compliant with the Convention on the Rights of Persons with Disabilities. Individuals whose childhoods are documented in records held by all entities providing care directly or indirectly should have a right to access records made about them. Full access should be given unless contrary to law. This includes the right to access records without redaction. Specific, not generic, explanations should be provided in any case where a record, or part of a record, is withheld or redacted. Consent of the person who is currently or was previously in care should be proactively sought if information needs to be shared with family members.

recommendation 116 in Detail

Recommendations by Commissioners Erueti and Gibson

Commissioners Erueti and Gibson consider the government should:

  1. develop, plan for, and establish an independent entity, as soon as possible, responsible for: 
    1. commissioning care and protection, youth justice, community mental health, disability and preventative services and supports from self-identified local (or in some cases, national) community groups and organisations (including hapū, iwi, urban Māori authorities, NGOs, Pacific, disability, mental distress communities, faith-based entities, and other collectives) across Aotearoa New Zealand.
    2. monitoring and evaluation of the delivery of care and protection, youth justice, community mental health, disability and preventative services and supports by local community groups and organisations to ensure that they are meeting the needs of individuals and whānau in their communities.
    3. investing in local community groups and organisations to build their capacity and capability to design and deliver these supports and services to meet the needs of their communities.
    4. reporting to government, Parliament and the public on the delivery of care and protection, youth justice, community mental health, disability and preventative services and supports by local community groups and organisations to ensure that they are meeting the needs of individuals and whānau in their communities.
  2. provide sufficient and sustainable investment to the Commissioning Agency to enable it to commission care and protection, youth justice, community mental health, disability and preventative supports and services that will meet the needs of individuals and whānau nationwide.
  3. transfer responsibility and investment for commissioning the following services and supports to the Commissioning Agency: 
    1. care and protection supports and services, from Oranga Tamariki.
    2. youth justice supports and services, from Oranga Tamariki.
    3. community mental health supports and services, from the Ministry of Health / Health New Zealand Te Whatu Ora.
    4. disability supports and services, from Whaikaha preventative supports and services, from Te Puni Kōkiri / Whānau Ora commissioning entities.
    5. preventative supports and services, from Te Puni Kōkiri / Whānau Ora commissioning entities.


Interim Recommendation 5 in Detail

The Crown should establish and fund a well-resourced independent Māori Collective made up of Māori with relevant expertise and/or personal experience and representing a mix of survivors, whānau, hapū and iwi, pan-tribal organisations and urban Māori with a fair mix of gender, LGBTQIA+, rangatahi and Deaf and disabled people to: 

  1. lead the design of the puretumu torowhānui scheme.
  2. work with survivors, the Purapura Ora Collective, survivors’ communities (including Māori, Pacific, Deaf and disabled communities) and other relevant groups to develop a plan to implement our recommendations, including: 
    1. establishing a puretumu torowhānui system underpinned by tikanga Māori.
    2. developing the process for applying for redress.
    3. determining what support and services are needed to respond to tūkino, enhance mana and achieve utua kia ea
    4. considering proposed civil litigation reforms.
  3. work with Māori survivors, whānau, hapū and iwi to: 
    1. explore whether to establish a separate puretumu torowhānui scheme for Māori.
    2. determine the nature, timing and content of an apology or apologies to Māori for abuse in care, as well as the nature of memorials to those abused.
  4. commission any reports, reviews or expert advice on areas considered important to the design of the puretumu torowhānui system and scheme, including an expert review of oranga services (see recommendation 68).
  5. build on this inquiry’s work by exploring how to respond to harm suffered by Māori in care to restore mana, tapu and mauri.
  6. work with the Crown and agree on the contents of any draft legislation required to give effect to any of the recommendations set out in this report.



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