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