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Charter for Action on Disability 

People with disabilities and their families/carers make up a large proportion of Victoria ’s population, but are a low priority for the Victorian Government. Support services are fragmented, under-resourced, and often ineffective. They are still organized around programs and bureaucracies, not around the persons with the disability and their families. The government’s rhetoric about treating people with disabilities and their families as valued partners is not reflected in practice. The gap between rhetoric and reality is huge

Urgent action is needed before the next state election to turn this around. As people with disabilities, their families, friends and supporters, we call on the Victorian Government to:
  
1. Include in Victorian disability legislation an entitlement to disability supports, prescribing minimum entitlements to people with disabilities over their life-cycle, and minimum entitlements to support for their families/carers.

2. Introduce legislated waiting time benchmarks for core services, and legal liability to the state for breaches of the benchmarks, including: 

a. A four week m
aximum wait for early childhood assessments; 
b. A six week ma
ximum wait for early childhood intervention programs; 
c. A six month maximum wait for emergency/urgent supported accommodation.

3. Introduce rigorous accountability mechanisms to make government departments and service agencies accountable to people with disabilities and their families, including:

a. An independent Disability Ombudsman;
b. An independent process of appeal and review concerning departmental decisions;
c. A ceiling of 35% on the amount that may be taken out of individual support packages as an administration component;
d. A duty of disclosure to recipients of individual support packages on the financial administration of packages;
e. A right for recipients of individual support packages to choose their own financial intermediary.

4. Support the establishment of a one-stop-shop Information Service, independent of government, to provide access information, comparative service quality data, and comparative price data on support services, accommodation services, respite services, health services and practitioners.

5. Table an annual report to parliament on progress in overhauling the day to day operation of the support system to:

a. remove ideological assumptions which pre-determine what people with disabilities and their families may choose as their living, educational and support arrangements;
b. ensure person-centred transferability of information to eliminate the need for multiple assessments and program duplication; and
c. ensure the effective participation of people with disabilities and their families as partners in the planning, design and delivery of supports.

6. Introduce a compliance and enforcement mechanism for making all public places, and services provided to the public, accessible to people with physical, sensory, neurological and developmental disabilities.

7. Make available an immediate supply of 1,000 places/beds/residences for crisis and emergency supported accommodation for families caring for people with severe and profound disabilities aged less than 65 years, and 200 accommodation options for young people currently living in inappropriate nursing homes.

8. Expand by threefold the number of people receiving individual support packages such as Support and Choice, Home First, Make a Difference, and Futures for Young Adults.
 
9. Introduce a Respite Entitlement assigned directly to caring families or their agents in the form of a respite service voucher, adjusted with a difficulty-in-caring rating, giving 6 weeks of respite per year to all primary caregivers. The Respite Entitlement should be used to purchase in-home respite or facility-based respite according to the preference of the family.

10. Introduce a Leave Entitlement assigned directly to people with disabilities or their agents in the form of a voucher giving 4 weeks leave and supports per year as a vacation/break from the primary care giver. 

Comments on the Charter are welcome and should be sent to Vern Hughes by email or on 0425 722 890.


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