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What are some alternative funding streams and supports that participants and their family members may be able to access via mainstream services (e.g., Medicare)?

1. Consider local providers, 2. Request support sessions that are less frequent and longer, 3. Avoid peak times, 4. Don't let providers dictate your supports

What the NDIS Code of Conduct sets out for providers and workers, and what My Plan Manager does to protect the health, safety & wellbeing of people with disability.

What are some creative ways participants can get more bang for their NDIS buck so they can access supports for the entire duration of their plans (e.g., booking therapy sessions that are less frequent, but run longer, to reduce overall spend on provider travel)?