Hunter Disability eNews

MAY 2004

Phone: 02 4927 0111 or e-mail: infoline@dash.org.au or web: www.dash.org.au

Welcome to the DASH Disability Infoline eNews. We aim to distribute the latest news relevant to the Hunter disability sector. To be added to or removed from our e-mailing list, simply send your name and e-mail address and request to infoline@dash.org.au. For contributions to eNews, e-mail any information to infoline@dash.org.au . Editor Evadne Lewis.

 

WHAT’S IN THIS EDITION:

 

1st – 31st MAY WORLD NEUROFIBROMATOSIS ** AWARENESS MONTH

10th – 16th MAY EPILEPSY AWARENESS WEEK

16th – 22nd MAY SCHIZOPHRENIA AWARENESS WEEK

24th – 29th MAY TOURETTE SYNDROME AWARENESS WEEK

31st MAY – 6th JUNE MACULAR DEGENERATION AWARENESS WEEK

 

HAPPENINGS

DISABILITY NETWORK HUNTER MEETINGS

DISABILITY NETWORK HUNTER QUIZ NIGHT 2004

THE ART GALLERY OF NEW SOUTH WALES – HANDS ON TOURS

MELBOURNE 2005 DEAFLYMPIC GAMES

 

CONFERENCES, WORKSHOPS AND TRAINING

ARATA 2004 NATIONAL CONFERENCE

QUALITY OF LIFE AND AGEING FOR PEOPLE WITH DISABILITIES

ADVOCACY IN ACTION

 

RESEARCH

PEOPLE WITH DISABILITIES LOSE OUT ON HOUSING

PSYCHIATRIC INPATIENT CARE FOR PEOPLE WHO ARE DEAF IMPULSE CONTROL DISORDERS
IN-PATIENT PSYCHIATRIC CARE FOR PEOPLE WITH INTELLECTUAL DISABILITIES
DESCRIPTIVE PSYCHOPATHOLOGY IN PEOPLE WITH INTELLECTUAL DISABILITIES
DEPRESSION IN YOUNG PEOPLE WITH INTELLECTUAL DISABILITY
ACCESS TO JOURNAL ARTICLES
ACCESS AND INCLUSION FOR DISABLED PEOPLE ON THE WORLD WIDE WEB

 

POLICY & DOCUMENTS
OMBUDSMAN TABLES REPORT INTO DADHC
MINISTER HAD ‘NO IDEA’ ABOUT DEPARTMENT FAILINGS
DEPARTMENT OF AGEING DISABILITY AND HOME CARE CALD JOINT ACTION PLAN
NESB RESPONSE TO DADHC DRAFT FUTURE DIRECTIONS DOCUMENT
$99m PACKAGE TO BENEFIT PEOPLE WITH DISABILITIES IN DISABILITY EMPLOYMENT SERVICES
MORE SUPPORT FOR CARERS IN $461 MILLION BUDGET PACKAGE
FUNDING FOR AUSLAN INTERPRETERS
DEMOCRATS RESPONSE TO THE BUDGET
CARERS’ CASH SLASHED - BY FLEUR ANDERSON – MAY 10, 2004 - THE DAILY TELEGRAPH

 

NOTICES
SUPPORTED OVERSEAS HOLIDAYS

PROVIDING A BREAK FOR CARERS

PREVENTATIVE WOMEN’S HEALTH CARE FOR WOMEN WITH DISABILITIES

WHAT IS DISABILITY?

SERVICES FIRST – NEW COALITION FORMED

NATIONAL FAMILY CARERS VOICE

AUSLAN ONLINE

DONATION

 

HAPPENINGS

DISABILITY NETWORK HUNTER MEETINGS

Future meetings of the Disability Network Hunter (DNH) will be held from 9.30am to 12 noon at the Warabrook Community Centre, 8 Angophora Drive, Warabrook. Dates for 2004: 28th April, 26th May, 30th June, 28th July, 25th August, 29th September, 27th October and 24th November. Could all members make attending the network a priority in 2004 so that we remain a unified voice in the Hunter. For more information contact: Bronwyn Shields, Secretary DNH, PO Box 2226, DANGAR NSW 2309. Tel: (02) 4925 2630 or Fax: (02) 4925 2646 or email: bshields@lwb.org.au

 

DISABILITY NETWORK HUNTER QUIZ NIGHT 2004

Disability Network Hunter (DNH) is holding its annual quiz night on Friday October 22nd  at South Newcastle Leagues Club, Llewellyn St, Merewether from 7.30 pm. Cost is $10 per person. The aim of the night is to raise money to create a fund to support the activities of International Day for People with a Disability (Dec 6th). There will be raffles, lucky door prizes and many other surprises. There is room for 20 teams of 10 or small organisations can join forces to make a table. For more information or an RSVP form, call David Hogg on: Tel (02) 4967 2172 or Bronwyn Shields on Tel: (02) 4925 2630.

 

THE ART GALLERY OF NEW SOUTH WALES – HANDS ON TOURS

In 2003 the Art Gallery of NSW introduced In Touch at the Gallery, a hands on tour for people who are blind or vision impaired. Visitors are able to experience the tactile qualities of marble, bronze and stone and discover the stories and ideas surrounding these unique objects. The tour has recently been expanded and now includes: figurative forms from Australia and Europe, focusing on the human body in 19th and 20th century sculpture, and a variety of stone and wood sculptures from the Gallery’s extensive Asian collections. Some of the objects are thousands of years old and come from a variety of cultures and religions. Visitors can choose to focus primarily on Asian or European works or on a mixture of both. In the future the Gallery hopes to introduce still more objects to ensure the tour is always a fresh and stimulating experience for visitors. 25 Volunteer Guides, some of whom have worked with visually impaired people in the past, have been specifically trained to guide the tour. Volunteers from the Royal Blind Society took part in a trial tour, and one of them, Donna Wilson, said the tour was "absolutely fantastic…having the opportunity to touch the sculptures made me realise there was so much intricate detail…eg. muscle tone. Even when I was less visually impaired than I am now, I was never able to see that amount of detail." Each tour consists of no more than five people to allow visitors to take their time with individual sculptures. Gloves are not worn, although visitors are asked to remove jewellery to avoid damage to the sculptures. The tour is also available to children and school groups and can be adapted to suit particular educational needs. In Touch Tours are available anytime during gallery opening hours, ie. daily 10am - 5pm, Wednesday until 9pm. (Closed Good Friday and Christmas Day.) Bookings are essential two weeks in advance. The Art Gallery is located in Art Gallery Road, The Domain, Sydney. Tel: (02) 9225 1740 or Toll Free 1800 679 278 or e-mail: amandap@ag.nsw.gov.au. Admission is free of charge.

 

MELBOURNE 2005 DEAFLYMPIC GAMES

The 20th Summer Deaflympic Games will be staged in Melbourne from 5th to 16th January 2005. The Games will be kicked off with a glittering Twilight Opening Ceremony Extravaganza, followed by an action packed 12 day sports program with over 3500 elite athletes from across the world. Tickets will go on sale on Monday May 31st 2004. Over 20,000 tickets will be available for sale, some sessions are limited in number, so early bookings are encouraged. 7 of the events will be FREE, only 2 venues, Melbourne Sports & Aquatic Centre (MSAC) and Olympic Park will have ticketed entry. Don't miss the opportunity of a lifetime to witness the very best of sport and celebration. To view the ticket prices and further information, go to: http://www.deaflympics.com/mel2005/sport_ticketingfinal.asp. [SOURCE: IDEAS Inc E-News Issue 9, 2004.]

 

 

CONFERENCES, WORKSHOPS AND TRAINING

 

ARATA 2004 NATIONAL CONFERENCE

Australian Rehabilitation and Assistive Technology Association (ARATA) is holding its 2004 national conference: Technology: everyone, everywhere, every day, from 2nd – 4th June 2004. The purpose of the association is to serve as a national forum for issues in rehabilitation and assistive technology. ARATA fosters interaction between all people with an interest in the field of rehabilitation and assistive technology and encourages research and development in this area. They participate in the development of standards and guidelines for quality assurance, service delivery, safety and ethics. The 2004 conference aims to enable participants to understand how the application of technology can allow inclusion of all people into everyday activities, home, school, work and leisure. For enquiries, contact: Conference Secretariat - A.M. Meetings Plus Pty Ltd, PO Box 16, Ascot Vale VIC 3032. Tel: (03) 9372 7182 or Fax: (03) 9372 7184 or email:arata@ammp.com.au. [SOURCE: IDEAS Inc E- News Issue 6, 2004.]

 

QUALITY OF LIFE AND AGEING FOR PEOPLE WITH DISABILITIES

A two day forum about issues of quality of life and ageing for people with disabilities through panel discussions and a series of speakers will be held 22nd – 23rd October, at Y on the Park Hotel, 5-11 Wentworth Avenue, Sydney. Speakers include: Roy Brown, Emeritus Professor from the University of Calgary and Flinders University; Dr Bob Schalock, University of Kansas; Professor Ivan Brown, University of Toronto; Dr Chris Bigby, La Trobe University and Professor Matt Janicki, State University of NY, Albany.  Contact the Centre for Developmental Disability Studies on Tel: (02) 8878 0500 or lpacheo@med.usyd.edu.au with any queries. Source: The Scene No.4. [SOURCE: IDEAS Inc E- News Issue 6, 2004.]

 

ADVOCACY IN ACTION

The Tamworth Belonging Conference, for people with a disability, family members, service providers and interested community members, was held at the Tamworth Community Centre on 24th March 2004. Local Aboriginal Elder Neville Sampson welcomed everyone to the region and said a few words of greeting in his traditional language. Local MP Peter Draper officially opened the conference and spoke about his mother's involvement in setting up the first special children's school in NSW. Then it was over to people with a disability to try to convey what belonging to the community means to them. Dale Givney spoke of his battle with a mental illness and the problems it had caused as he was trying to raise his son. Uma Raj talked about the difficulties she faced, because of her visual impairment, when seeking employment. Being a wheelchair user because of a spinal injury, I spoke about access and how much more enjoyable life is if you can easily access things in the community. After morning tea, Mark Daly of Advocacy Northwest, Ruth Jacka of MDAA and Suriya Lee of NSW Disability Council talked about ways the community can include people with disabilities and why it is important that this happen. It was interesting to listen to their differing perspectives and encouraging knowing that there are people like them working to ensure that people with a disability are treated fairly in the community. After a very tasty lunch, we split into several groups to work through a list of questions. This generated some very thought-provoking discussion and was a rewarding and beneficial end to the day. I'm sure a lot of people gained valuable insight into disability issues from this part of the day, and no doubt would have gone away with a good deal more knowledge and understanding of the problems faced by people with a disability in the community. Congratulations to everyone involved in the organisation of the day. [SOURCE: Ross Webeck, New England Representative for ParaQuad NSW.]

 

 

RESEARCH

 

PEOPLE WITH DISABILITIES LOSE OUT ON HOUSING

Bostock, L. and Gleeson, B. Contested Housing Landscapes? Social Inclusion, Deinstitutionalisation and Housing Policy in Australia. The Australian Journal of Social Issues, 39 (1), 41-62. The article may be freely downloaded from www.acoss.org.au. Gary Moore, Director of NCOSS, commented on the research: This research highlights what many people on the ground know, there is too little affordable housing and too few housing support services for people with disabilities. The research predicts that in the period to 2010 around 3,500 people with disabilities (mostly intellectual) in Australia and 2,500 in NSW will leave institutions. The research shows that at present NSW has the largest number of people with disabilities in institutions of any state of Australia and has been among the slowest in the country to address the problem of institutionalisation. These institutions are policy left-overs from the nineteenth century. State and national governments have separate Housing and Disability agreements but politics has meant that these two areas do not come together to ensure that there are adequate public and community housing options for people with disabilities. People with disabilities are the most aggrieved victims of the housing crisis. Nearly $1.2 billion of tax is foregone on negative gearing in Australia, which is delivering rental growth only at the top end of the housing market. Co-author of the research, Professor Brendan Gleeson of Griffith University said: Too often when community or group homes are being established for people with disabilities, the NIMBY (not-in-my-backyard) problem arises. Neighbours complain and as a result we risk creating ghettos in poor suburbs. It would be a tragedy if as a community we fail to get people with disabilities out of these institutions. However we need to ensure there are viable housing options and choices, not just turning people out of one inadequate institution into another. As a result of a lack of housing and support services too many people with disabilities are homeless or forced to make use of emergency housing, hospitals or, worst of all, go into the prison system. [SOURCE: IDEAS Inc E- News Issue 6, 2004.]

 

PSYCHIATRIC INPATIENT CARE FOR PEOPLE WHO ARE DEAF

The unique treatment needs of psychiatric inpatients who are deaf require added dimensions to their care. Because of the scarcity of specialised units for persons who are deaf, descriptions of these treatment needs are infrequent. This study assessed diagnoses and linguistic and cognitive co-morbidities in this population. A total of 62 percent of the inpatient sample had major mental illnesses, 58 percent had psychotic illnesses, and 26 percent had a dual diagnosis of a mental disorder and substance use disorder. Case examples illustrate some of the unique characteristics of these patients. The broad reasons for admission are illustrated, as are some of the treatment adaptations made by a specialised unit for deaf persons. [SOURCE: Haskins, B.G. (2004) Serving Deaf Adult Psychiatric Inpatients. Psychiatric Services, 55, 439-441.]

 

IMPULSE CONTROL DISORDERS
This article reviews the current knowledge of the clinical characteristics and pharmacological management of pathological gambling, kleptomania and compulsive buying. Specifically the article summarises the phenomenology and associated psychopathology of these disorders and presents study results of the various pharmacological agents used to treat these disorders: serotonin reuptake inhibitors, opioid antagonists, mood stabilisers and atypical antipsychotics. [SOURCE: Grant, J.E. and Potenza, M.N. (2004) Impulse control disorders: clinical characteristics and pharmacological management. Annals of Clinical Psychiatry, 16, 27-34.]

IN-PATIENT PSYCHIATRIC CARE FOR PEOPLE WITH INTELLECTUAL DISABILITIES
Little is known about the experiences of individuals with intellectual disabilities and additional mental health problems who are admitted for inpatient psychiatric care. In the UK such care is delivered in both generic psychiatric and specialised treatment settings. The present study explored service users' and carers' views on in-patient psychiatric treatment received across these two settings. Thirty service users and wherever possible their main carers were interviewed about their views on the psychiatric admission, treatment and discharge process. Data was gathered during semi-structured, one-to-one interviews. Both service users and carers identified positive and negative aspects of the psychiatric admission. For service users: lack of control and information, support from staff, or conversely its absence emerged as key themes. For carers: concerns about service users' vulnerability, negative staff attitudes and opportunities for involvement emerged as key themes. The accounts of both groups regarding generic psychiatric settings were predominantly negative. In contrast, specialised settings were frequently described as providing a pleasant environment, supportive and caring staff, good information sharing and satisfactory discharge arrangements. Conclusions: important areas for service improvements are highlighted, implications for generic settings in particular are considered. [SOURCE: Longo, S. & Scior, K. (2004) In-patient psychiatric care for individuals with intellectual disabilities: the service users' and carers' perspectives. Journal of Mental Health, 13(2), 211-221.]

 

DESCRIPTIVE PSYCHOPATHOLOGY IN PEOPLE WITH INTELLECTUAL DISABILITIES
This article considers variables associated with the presence of a psychiatric diagnosis in those referred to a specialist mental health service for people with mental retardation (MR). Data were collected on 752 newly referred clients. The presence of a psychiatric diagnosis was assessed by two psychiatrists, based on International Classification of Diseases (10th Rev.) criteria. A series of binary logistic regression analyses were conducted. Older age, mild MR, admission to an inpatient unit, referral from generic mental health services, and detention under current mental health legislation were associated with an increased presence of any psychopathology. Severe MR, the presence of epilepsy, and residence with the family were associated with a lower incidence of any psychopathology. Findings relating to specific psychiatric diagnoses on the whole supported previous research. Clear service arrangements are necessary for people with mild MR who have a high incidence of psychiatric disorders. [SOURCE: Cowley, A., Holt, G., Bouras, N., Sturmey, P., Newton, J.T. & Costello, H. (2004) Descriptive Psychopathology in People With Mental Retardation. Journal of Nervous & Mental Disease, 192(3), 232-237.]

DEPRESSION IN YOUNG PEOPLE WITH INTELLECTUAL DISABILITY
Discusses various myths and clinical issues on the topic of depression and intellectual disability. [SOURCE: Dossetor, D. (2002) Depression in young people with intellectual disability. the Clinician, 2(1), (Courage and depression), 28-33.]

ACCESS TO JOURNAL ARTICLES
Access to the full-text of the journal articles referenced above is available through the James Fletcher Library, located on the first floor of the Barracks building in the grounds of James Fletcher Hospital, Watt St, Newcastle. For more information contact the library on Tel: (02) 4924 6790 or Fax: (02) 4924 6795 or email: jfhlibrary@hunter.health.nsw.gov.au or website: www.himh.org.au - select “James Fletcher Library” – then scroll down to “click here for more information”.

ACCESS AND INCLUSION FOR DISABLED PEOPLE ON THE WORLD WIDE WEB
According to a study published 15th April 2004 by the Disability Rights Commission (DRC) UK, more than 80% of UK public websites fail minimum standards for disabled web access. Many disabled people find it impossible to book a holiday, open a bank account or buy theatre tickets online. The DRC issued a stern warning that many businesses may not be complying with existing equal access laws and it was only a matter of time before they faced legal challenge from disabled consumers. The study also revealed high levels of ignorance among web developers over both the steps required and the costs of making their websites accessible for disabled people. With the Centre for Human Computer Interaction Design at London's City University, the DRC looked at a representative sample of 1,000 public websites. 100 sites were subjected to in-depth evaluation by a disabled users’ group, who had a range of impairments. Researchers also canvassed the views of more than 700 businesses that had commissioned websites and nearly 400 website developers. Automated software tools, used to test whether the sample sites complied with voluntary web access guidelines set by the World Wide Web Consortium, revealed that 81% of websites (808) failed to meet minimum standards for disabled web access. The survey also found that the average home page contains 108 barriers that make it impossible or very difficult for disabled people to use. The evaluation of 100 websites by the disabled user group revealed that because of poor accessibility over a quarter of the most routine and straightforward online tasks could not be completed successfully. Blind people were the most disenfranchised of web users, as they were unable to perform nearly half the tasks set them despite using devices such as screen readers. In the same study, the DRC found that levels of accessibility expertise amongst website developers were low with only 9% using disabled people to test their sites. You can download the report at: www.drc-gb.org/publicationsandreports/report.asp. Source: Disabled Rights Commission Website - 2004. [SOURCE: In the Media - Physical Disability Council of NSW www.pdcnsw.org.au.]

 

POLICY & DOCUMENTS

OMBUDSMAN TABLES REPORT INTO DADHC
The NSW Ombudsman, Bruce Barbour, recently released a special report to Parliament, which highlights the failure of the Department of Ageing, Disability and Home Care (DADHC) to effectively support families at risk of giving up the care of their disabled children. The report details the findings of an extensive investigation. Mr Barbour said: “My investigation shows that DADHC has failed to adequately support families to enable children with disabilities to remain in the care of their family. Many families who care for children with disabilities already face significant stress. The result of DADHC’s ineffective intervention was that this stress was unduly aggravated.” The Ombudsman investigation found that the department’s implementation of its policy for children and young people with disabilities demonstrated: lack of clarity about the department’s role in supporting families in crisis; uncertainty about which sections of the department had responsibility for providing support; confusion about the respective roles of DADHC and the Department of Community Services (DoCS); inconsistencies in DADHC’s own policy requirements; inadequate guidance to staff about how to implement the policy and subsequent confusion about how services should be provided. The Ombudsman said: “a major concern was that families were not able to get the services necessary to support them through difficult times”. The investigation found: confusion about how to obtain access to services; no clearly defined decision making process about access to services; a fragmented and poorly co-ordinated service system and no clearly defined avenue of appeal where services were denied or considered inadequate. The Ombudsman investigation also found that, for children with disabilities who were not able to remain living with their families, service arrangements were often inadequate. “These children were not provided with the same safeguards as children who enter care through the child welfare system.” The Ombudsman said: “DADHC has responded to our investigation in a positive way by developing an action plan and establishing a task force to address the problems we have highlighted”. Strategies within the action plan include addressing staff training needs, implementing an effective system to deal with requests for support, enhancing service access and coordination and improving the range of available services. “The key to the department’s improvement in this area will be effective implementation of its action plan. It is an ambitious plan and we will be closely monitoring the department’s progress over the coming year.” The report, including the DADHC Action Plan, can be found at: www.nswombudsman.nsw.gov.au/publications/index.html. [SOURCE: IDEAS Inc E-News Issue 9, 2004.]

MINISTER HAD ‘NO IDEA’ ABOUT DEPARTMENT FAILINGS
NSW Community Services Minister Carmel Tebbutt has stated she had no idea about widespread mismanagement within her department despite the Ombudsman finding major failings. Ombudsman Bruce Barbour's report found support for families by the disabilities department was so inadequate, many have been forced to place their children in outside care. It says a policy was put in place in 2002 to keep families together but two years later it was still failing. Ms Tebbutt says an action plan has now been put in place and has blamed the department for the problems. "The Ombudsman's identified some serious weaknesses in the way the department has implemented its children's policy," she said. "The department's developed a comprehensive action plan to address those issues, my responsibility is to ensure that action plan is implemented." [SOURCE: IDEAS Inc E-News Issue 9, 2004.]

DEPARTMENT OF AGEING DISABILITY AND HOME CARE CALD JOINT ACTION PLAN
The Multicultural Disability Advocacy Association (MDAA), together with 20 other agencies, has participated in the development of a CALD (Culturally and Linguistically Diverse) Joint Action Plan. DADHC recently signed off this plan as their commitment to a partnership approach to improving accessibility and responsiveness of services for people with a disability, older people and their carers from CALD backgrounds. DADHC see this as demonstrating ’shared commitment in improving access and responsiveness of services’ and operate from the perspective that all participating organisations are recognised as equal partners in the formulation and implementation of the Joint Action Plan. MDAA continue to express their concerns with this plan. They are particularly disturbed about the lack of any commitment to improving access and responsiveness of DADHC provided services, as well as a lack of any significant initiatives to enhance access for people to DADHC funded services. MDAA is also disappointed about the plan’s short time frame (June 2004). They are concerned that this represents a piecemeal approach that achieves little but placates critics. [SOURCE: MDAA March eNews.] More information about CALD activities can be found in the newsletter: Synergy (2004) No. 1, published by Multicultural Mental Health Australia. Their web address is: www.mmha.org.au.

NESB RESPONSE TO DADHC DRAFT FUTURE DIRECTIONS DOCUMENT
MDAA together with the ECC and with endorsement from a range of organisations, including ACROD and NCOSS, responded to the DADHC draft Future Directions document: www.dadhc.nsw.gov.au/dadhc/Doing+business+with+us/DADHC+Future+Directions+2004+-+A+Draft+Discussion+Document.htm. This response recommends strategic directions for the Department to address current racial inequities: www.mdaa.org.au/systemic/04/response.dadhacpaper.html. One of the key recommendations is that DADHC establish broad performance targets in collaboration with stakeholders that increase incrementally to achieve equity over the next 10 years. In practice, they recommend that regional DADHC offices assist agencies to develop targets to ensure that, over time, the agencies’ consumers reflect the cultural diversity of the community the agency serves. 3 out of every 4 people from a NESB with disability continue to miss out on Disability Services. MDAA strongly believes that unless serious commitments (such as outcome targets) are made to redress these appalling service utilisation rates, DADHC and the NSW Labor government continue to operate a system that is not based on need but one that is based on race. If you have any queries, questions, comments or other contributions contact MDAA by email: mdaa@mdaa.org.au or Tel: (02) 9891 6400. [SOURCE: Disability and NESB – May 2004, a newsletter produced by MDAA.]

$99m PACKAGE TO BENEFIT PEOPLE WITH DISABILITIES IN DISABILITY EMPLOYMENT SERVICES
On the 21st April 2004, the Federal Government announced a $99 million assistance package to ensure that employees with disabilities receive pro-rata award-based wages and have better access to quality services and personalised workplace training and support. Announcing the new package with the Prime Minister, the Minister for Family and Community Services, Senator Kay Patterson said the $99 million in new spending over the next four years was designed to deliver quality services and good working conditions to the 17,000 Australians with a disability working in business services. "It is important that we ensure that business services are viable and can operate successful businesses in the future," she said. The package includes: a range of strategies that ensures that no person will be displaced from a service and no sole service in a town or region will close due to the current changes to the sector; assistance to address the effect of increased wages; the release of new pricing models for both business services and open employment services to provide fairer and more efficient funding; and the release of the business services wage assessment tool, which has been developed by the Australian Government in consultation with provider, consumer, business and union representatives, to assist business services determine fair pro-rata wages for employees with disabilities. Senator Patterson said: "The Government-funded wage assessment tool is available for business services to calculate pro-rata award based wage levels for their employees. The release of the new wage assessment tool will deliver fairer wages for business service workers because it will determine a pro-rata wage, based on productivity and competency of each individual. Through the industry assistance measures, the Australian Government will provide extra support for people whose productivity is very low and who choose to continue working with their business service. Eligible clients can have access to a case manager to support them in choosing whether they wish to remain working in the business service, undertake training at their current service, enter a targeted support service or work in an alternative service.” Senator Patterson said case-based funding is a fairer system where disability employment services will receive funding based on the individual support needs of their employees. "Over the next 18 months providers will be gradually converted to the new system and will receive extensive support from the government during this process.” Source: Minister for Family and Community Services - Media Release 2004. [SOURCE:  In the Media - Physical Disability Council of NSW www.pdcnsw.org.au.]

MORE SUPPORT FOR CARERS IN $461 MILLION BUDGET PACKAGE
A one-off boost of up to $1000 for carers, an extension of Carer Allowance and more support for young carers and elderly parents caring for a son or daughter with disabilities are part of a $461 million Carers Package in the 2004-05 Budget. The Minister for Family and Community Services, Senator Kay Patterson, said the Australian Government was committed to providing strong support for carers and recognising the valuable role they play in the community. The new support for carers includes a one-off Carers Bonus of $1000 to eligible recipients of Carer Payment and $600 to each recipient of Carer Allowance, to be payable before the end of June 2004. Carer Allowance has been extended to carers who do not live with the people for whom they provide care. To qualify they must provide a minimum of 20 hours a week of personal care and the receiver of the care must be assessed as needing that level of care. The changes will be implemented from 1
st April 2005. Young carers, who are at risk of leaving school early, will be provided with in-home respite services of up to five hours each school week to help them complete their secondary or vocational equivalent education and at risk young carers will get one fortnight of respite care each year to undertake activities such as studying for exams, training or recreation. All young carers would have access to information, advice and referral services through a telephone hotline, on line advice and an information package. The Federal government will work with the State and Territory governments to provide a guarantee that respite care will be made available for ageing parents caring for a son or daughter with a disability. For example, four weeks a year respite for parents over 70 years of age who are caring for a son or daughter with a disability. Parents aged 65 to 69 who care for a son or daughter with a disability and need to spend time in hospital will be eligible for up to two weeks respite care. Ageing parents are often worried about how their children will be helped into disability accommodation when they can no longer provide care. The government proposes that the Community and Disability Services Ministerial Council establish an advisory body to develop options. Source: ACOSS Media Release 11 May 2004. [SOURCE: In the Media - Physical Disability Council of NSW
www.pdcnsw.org.au.]

FUNDING FOR AUSLAN INTERPRETERS
The 2004-05 Budget announcement of $18.4m over four years to establish a unit to book and pay for Auslan (Australian Sign Language) interpreters for specified private medical and health consultations brings a welcome relief to Australia's Deaf community. "We're delighted!" said Australian Association of the Deaf (AAD) manager Karen Lloyd. "Deaf people have been struggling for years without an interpreter at medical appointments, and Deaf Societies have been struggling without funds to provide interpreters when they can. Deaf people need to be able to understand information about their health, and the most effective way to do this is via Auslan interpreting. This funding will go a long way to addressing a real need." For further information on AAD, contact Karen Lloyd on TTY: (07) 3357 8277 or Tel: (07) 3357 8266 or Fax: (07) 3357 8377 or email:
karen.lloyd@aad.org.au. or web-site: www.aad.org.au. Source: Australian Association of the Deaf - Media Release 2004. [SOURCE: In the Media - Physical Disability Council of NSW
www.pdcnsw.org.au.]

DEMOCRATS RESPONSE TO THE BUDGET
The 2004-05 Budget offers plenty of assistance for people already in the workforce and earning high incomes, but nothing to assist people with disabilities to move out of poverty into open employment, or out of aged care nursing homes into more suitable accommodation. Australian Democrats spokesperson for Family & Community Services and Disability, Senator Brian Greig, says the Budget is heavily weighted in favour of high income, working families to the detriment of single parent families and people with a disability. "People with a disability missed out on the $300 lump payment in the last pre-election budget and now miss out again on any lump sum payments. The Government is offering lump sum one-off payments of $600 to families, $1000 to carers, $3500 to aged care facilities for residents, but nothing to those with a disability," Senator Greig said. "In spite of an injection of $2.2 billion into aged care, there is nothing for young people with disabilities trapped in nursing homes, with low levels of rehabilitative support. People with a disability have the same needs as other low income Australians, but they do not qualify for the tax cuts. Few will have the opportunity to contribute to superannuation and they will therefore not benefit from the Government's co-contribution incentives."  Senator Greig says it appears that this section of Australian society is being made to pay for the Senate's decision last year to reject the severe cuts to disability support pensions that were proposed by the Government. "The pay rise in the Budget is good news for those currently working in business services, but there is little to assist those who are able to move from the old sheltered workshops into mainstream employment. All the reforms of the McClure Report that would have helped people with a disability have been ignored now for three years, they may well disappear into history. The Democrats are again calling on the Government to recognise the cost of disability, pay tiered income support and at least provide a one-off payment from this year's generous surplus. Media Contact: Di Graham, Tel: (02) 6277 3338 or 0417 177 523. Source: Democrats - Media Release 2004. [SOURCE: In the Media - Physical Disability Council of NSW www.pdcnsw.org.au.]

CARERS’ CASH SLASHED - BY FLEUR ANDERSON – MAY 10, 2004 - THE DAILY TELEGRAPH
Parents caring for disabled children will be hit by a $104 million cost-cutting scheme to be introduced after the federal election, leaked Cabinet documents reveal. Almost 43,000 parents with seriously sick or disabled children, and adults caring for their elderly parents, would have their maximum backdated carers' allowance slashed from $2280 for a year to just $526 for a maximum three months. The cost savings will pay for a separate $107 million four-year package for carers the Federal Government is expected to reveal tomorrow and estimated to benefit just 13,000 people. Under that package, carers would be able to claim the $90-a-fortnight carers' allowance, even if they are not living in the home of the person they are caring for. The confidential Cabinet paper said reducing the amount of backdated time carers claimed would produce ongoing and increasing savings for the Government. The cost-cutting measure would be introduced in July 2005, saving the Federal Government $33.6 million in 2005-2006, $35.1 million in 2006-2007 and $36 million in 2007-2008. The Federal Government previously tried to slash the backdated carers' allowance in 1997 but failed to get the proposal through the Senate. "The Senate argued that the proposal failed to recognise the hardship experienced by parents of children with disabilities, especially those children with conditions that take a long time to diagnose," the document said. Opposition family and community services spokesman Wayne Swan said families faced enormous financial pressures when a family member fell seriously ill because often another family member would have to give up work to care for them. Under the current arrangements, a carer's allowance can be backdated for up to 52 weeks prior to the date the allowance is first claimed for a sick child and up to 26 weeks for an adult. That would now be cut back to a maximum of 12 weeks. The allowance is meant to signify the Australian Government's appreciation of carers. "The proposal would standardise the carer's allowance backdating provisions for adults and children, remove inequities in the current arrangements and remove confusion for customers about different backdating rules," the Cabinet document said. "The proposal would affect 42,750 new claimants of carers' allowance by reducing the amount of back payment received when carers' allowance is granted." It would not affect people currently claiming the allowance or the numbers of people granted the allowances. [SOURCE: In the Media - Physical Disability Council of NSW www.pdcnsw.org.au.]

 

NOTICES

SUPPORTED OVERSEAS HOLIDAYS
Eagleton Ridge Respite Centre Pty Ltd has branched into Supported Overseas Holidays. Our first trip is to Bali in June 2004. 8 days & 7 nights in 5* Resort Accommodation, includes airfares, airport taxes accommodation, meals, tours, transport and 24 hour support. Holidays planned for June, September, December, March and June, depending on availability. Please contact Belinda Furlonger, Director, Eagleton Ridge Respite Centre Pty Ltd on Tel: (02) 4987 1686 for further information.

PROVIDING A BREAK FOR CARERS

The Commonwealth Carer Respite Centre provides support for the carers of younger people with moderate, severe or profound disabilities, frail older people, people with a terminal illness in need of palliative care, people with dementia and people with dementia and challenging behaviours. A carer is a person such as a family member, friend or neighbour, who provides regular care and assistance to this person on an ongoing basis. Respite provides a break from the responsibility of the caring role which while often rewarding, can also be very stressful. Respite can be organised for a few hours, a day, a night or longer for emergency, short-term and planned breaks. Carers who need a break should call 1800 059 059 to discuss their respite needs and to plan a break which is suitable to their individual situation.

 

NATIONAL FAMILY CARERS VOICE

Representing unpaid family carers of people who were born with or acquired a disability or medical condition prior to the age of sixty-five. The National Family Carers Voice (NFCV) met with Minister Kay Patterson in Melbourne on 17th  March 2004 to discuss the results of a survey conducted earlier this year. Over 1000 responses were received and have been analysed. It was accepted that the survey results were representative, rather than comprehensive. The data identified both structural and general issues that impact on family carers. NFCV decided the issues impacting on family carers would be addressed in a three-stage process: development of an issues paper, preparation of preliminary recommendations for the Minister by May/June and writing a final report addressing structural and strategic issues. Preliminary work on the issues paper has begun and a task force will continue to work on it. For further information contact: National Family Carers Voice Secretariat, CE3 – TOP, Box 7788, Canberra Mail Centre ACT 2610. Tel: (02) 6244 1849 (or 1300 653 227, asking for extension 441849) or Fax: (02) 6244 7976 or e-mail: nfcv@facs.gov.au. [SOURCE: IDEAS Inc E- News Issue 6, 2004.]

 

PREVENTATIVE WOMEN’S HEALTH CARE FOR WOMEN WITH DISABILITIES

The NSW Cervical Screening Program has identified women with disabilities as a group that are under-screened with respect to cervical screening. To address this the NSW Cervical Screening Program, together with the Centre for Developmental Disability Studies, has developed a set of guidelines on preventative women’s health care for women with disabilities. The guidelines were developed in response to concerns that women with disabilities may not receive the same level of preventative women’s health care as other women. The guidelines are based on the best evidence available at the time of publication and are intended as a guide to general practitioners and service providers. They were developed with the involvement of key stakeholder groups, including both consumers and clinicians. Copies of the guidelines can be obtained by phoning the NSW Cervical Screening Program on Toll free: 131 556 or accessing the program’s web-site at: www.csp.nsw.gov.au.

 

WHAT IS DISABILITY?

The Multicultural Disability Advocacy Association (MDAA) is conducting a project entitled: What is disability? - to enhance knowledge and reduce stigma about disability and disability-related issues in culturally and linguistically diverse (CALD) communities. The project aims to provide information to 10 ethnic communities in community languages, starting from the understanding each community has about disability and people with a disability. For further information about the project, contact MDAA on: Tel: (02) 9891 6400 or Toll-free: 1800 629 072 or Fax: (02) 9635 5355 or TTY: (02) 9687 6325 or email: mdaa@mdaa.org.au or web-site: www.mdaa.org.au. [SOURCE: Synergy (2004) No. 1.]

 

SERVICES FIRST – NEW COALITION FORMED

We are in what is likely to be a federal election year. The Australian Government has a hefty budget surplus. One of the biggest issues will be whether this is used to improve health, education and community services or to fund income tax cuts. A new group called Services First has been formed to raise awareness in the community of the importance of health education and community services, the serious problems that beset them, and the risk to their viability posed by another round of tax cuts at this time. Membership of Services First is diverse: it includes organisations representing services providers and consumers. At this stage, participating organisations include the National Public Hospital Clinicians Task Force, the Royal Australian College of General Practitioners, the Aboriginal and Torres Strait Islander Commission, the Disability Federation of Australia, Aged and Community Services Australia, the Australian Council of State School Organisations, the Australian Education Union, the National Tertiary Education Union, the Australian Council of Social Service and National Shelter. The goal of Services First is to get the parties to give priority to investment in services, and better family and social security payments instead of tax cuts, at least over the term of the next Government (the next 3 years). Services First is non-partisan. It will not endorse or support any political party or candidate for election.  However, it will focus on media and marginal electorates to ensure that their message, the need to improve services, gets through in this election year. You can get further information about Services First from its web site at www.servicesfirst.org.au. [SOURCE: IDEAS Inc E- News Issue 6, 2004.]

 

AUSLAN ONLINE

The Royal Institute for Deaf and Blind Children will soon launch the world’s first virtual linguistic community. A seeding grant from the Telstra Foundation has enabled Associate Professor Trevor Johnston to work on ‘SignBank’, an interactive dictionary web site of Auslan — a natural sign language used by Australia’s Deaf community. Professor Johnston said that currently there are problems with uncoordinated sign innovation and SignBank will help to bridge this gap. Users will be able to enter signs into the SignBank web site in a simple, graphically based way and also register their approval or disapproval of sign innovations, immediately displayed as part of the site's community feedback. For more information contact Kath Keenan on Tel: 0408 408 497 or (02) 9872 0304 or email:kath.keenan@ridbc.org.au. [SOURCE: Acrod News April 2004.]

 

DONATION

To give away to a good home (totally for free) – a Gother 3 wheel electric scooter. Good condition. Needs new battery charger. Contact Arthur Woolley on Tel: (02) 4970 5336.

 

 ** Neurofibromatosis (NF) is an inheritable disorder characterised by benign tumours which form in and around nerves in various parts of the body, particularly the skin. NF is caused by a faulty gene and children of a person with NF each have a 50 % chance of inheriting the disorder. However, the disorder can sometimes occur when there is no family history, due to a spontaneous gene mutation. There are two types of NF: Neurofibromatosis Type 1 (NF1), also known as von Recklinghausen's disease and Neurofibromatosis Type 2 (NF2), also known as bilateral acoustic neurofibromatosis. They are genetically distinct disorders, caused by faults in two different genes. NF1 is the most common, around nine out of 10 people with NF have NF1. It is thought to affect 3-4,000 people in Australia. The symptoms vary widely from person to person, some of the characteristics are: café-au-lait spots (patches the colour of milky coffee, which develop on the skin, triggered by an accumulation of skin pigment), freckles on the skin, particularly around the underarms and groin and Lisch nodules (tiny lumps) which develop inside the iris (but don’t affect vision) and can usually only be seen with a special lamp. Each person with NF1, even within the same family, can be affected differently. The most common other features are: Plexiform neuromas (large lumps, involving groups of nerves, the symptoms depend on which nerves are compromised), learning difficulties and scoliosis (curvature of the spine). NF2 often affects auditory nerves. Around five per cent of people with NF have NF2. It is estimated that about 1 in 40,000 people are affected. It is distinguished by the development of benign tumours on one or both auditory nerves. Tumours may also occur on the spinal cord and other parts of the central nervous system. People affected by NF2 may also experience: spasms of their facial muscles, generalised muscle weakness, numbness, pain, partial paralysis, impaired speech and hearing and balance problems. There is no standard treatment for NF, options may include: surgery to remove problematic tumours; therapy to help the person to achieve their full potential, including speech therapy and physiotherapy; surgical removal of cancerous tumours and appropriate treatment, such as chemotherapy or radiotherapy and genetic counseling. More information can be located at: www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Neurofibromatosis?open.