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Full paper text [PDF 3515k] - New Zealand Parliament

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22<br />

Right 4 is clearly a major factor for all<br />

sectors, with 43% of complaints about<br />

disability services, 53% of complaints about<br />

health services and 37% of those involving<br />

mental health providers relating to<br />

standards of care. The combined complaints<br />

about communication, information and<br />

consent (Rights 5, 6 and 7) featured in 39%<br />

of complaints about disability services<br />

(up from 36% in the previous year), 33%<br />

of complaints about health providers and<br />

37% of complaints about mental health<br />

providers. The right to support (Right 8)<br />

continues to feature in just 2% of disability<br />

complaints, compared with 1% of health<br />

and 6% of mental health complaints.<br />

The complaint process (Right 10) featured in<br />

4% of the complaints about both disability<br />

and mental health services, compared with<br />

2% of complaints about health services.<br />

Demographics<br />

In 2011/12 more complaints came from<br />

female callers (56.7%) than male callers<br />

(38.3%). People who described their gender<br />

as “other” made up the remaining 5% of<br />

complainants. Consumers under the age<br />

of 15 years accounted for 4% of complaints.<br />

At 34%, the highest number of complaints<br />

was made by people in the 41–60 age<br />

group followed by 27% from the 26–40<br />

age group and 23% being about consumers<br />

aged between 61 and 90 years of age.<br />

<strong>New</strong> <strong>Zealand</strong> Pakeha continued to make<br />

the largest number of complaints (67%)<br />

with <strong>New</strong> <strong>Zealand</strong> Maori making 13% of<br />

the complaints. Pacifi c people made 2%<br />

of complaints in 2011/12. The remainder<br />

of complaints were from a wide range of<br />

ethnic groups, including a small group of<br />

people who declined to provide<br />

their ethnicity.<br />

Residential visits<br />

Advocates have been visiting rest homes<br />

for six years and disability homes for fi ve<br />

years. The purpose of the visits is to make<br />

it easy for residents to speak with an<br />

advocate and to provide free education<br />

sessions for residents and whanau/family<br />

members as well as providers. All but one<br />

of the 680 rest homes had at least one<br />

contact with an advocate, and 506 rest<br />

homes had at least two contacts. Advocates<br />

made at least one contact with 957 of 961<br />

disability homes and 657 had at least two<br />

contacts. Over the reporting year, there have<br />

been a total of 3,069 rest home and 3,074<br />

disability residential visits by advocates.<br />

Every residential home has been given a<br />

free copy of the Tell Someone DVD. The<br />

DVD is an educational tool to help people<br />

with learning or intellectual disabilities<br />

understand their rights. About 10% of the<br />

visits have been to assist residents and/or a<br />

third party acting on behalf of the resident<br />

to make a complaint.<br />

Networking<br />

Networking is an important way for<br />

advocates to establish a profi le in their local<br />

communities so they are well positioned<br />

to inform consumers of their rights and<br />

providers of their duties. Networking helps<br />

advocates make effective referrals if the<br />

matter is outside the HDC’s jurisdiction.<br />

Networking and education are the key<br />

features of the role of the six specialist<br />

advocates. These advocates respond to<br />

the needs of a range of Deaf, refugee and<br />

migrant communities. Over the past year<br />

advocates developed and maintained<br />

contact with 4,189 networks, of which 46%<br />

had a disability focus, 3% were with Maori<br />

networks and 6% were with refugee and<br />

migrant communities from non-English<br />

speaking countries.

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