Rights and wellbeing
Disability rights, wellbeing and everyday choice
Disability rights include having a say, being treated with respect and making choices about your life. Those experiences matter in support relationships, at home and in the wider community. This collection brings them together with practical information about advocacy, safety and wellbeing.
You will find articles about making choices, raising concerns and supporting someone to speak for themselves. There are also stories about identity, relationships, family life, emotional wellbeing and peer connection. Some are personal accounts; others offer questions or approaches you can use in everyday conversations. The author's perspective remains part of the story, rather than a rule about how everyone should feel.
For participants, these topics can help put words to an experience or prepare for a conversation about support. You might want more privacy, a different way of communicating or a clearer explanation of a decision. Families and carers can think about how to offer help while respecting the person's own wishes. Providers and workers can reflect on the effect of everyday practices, including how they listen and respond when someone disagrees.
The NDIS Code of Conduct sets expectations for providers and workers, including respect for individual rights and privacy. If something has gone wrong with an NDIS service, the NDIS Commission provides information about reporting concerns and making complaints. The right next step depends on the issue and the support you need.
Wellbeing and belonging are broader than a funding plan. Community groups, trusted people and health services can also be important sources of support.
Browse this collection for practical help, a different perspective or a story that resonates with you. You do not need to share someone else's experience for it to prompt a useful question about your own life, relationships or the support you receive.
Subcategories
Articles
- NDIS public debate: stories, evidence and the fraud narrative
- Autism parenting: recognise progress that matters to your child
- A family’s NDIS journey: advocacy, change and reliable support
- NDIS Emergency Planning: Protect Your Safety and Keep Support Going
- A mother and daughter’s advocacy story: Alana’s reflection
- Judy Heumann: disability rights, advocacy and her legacy
- Love and disability: relationships without assumptions
- Wellbeing on difficult days: a lockdown-era perspective
- Living with SMA: Rachel’s risdiplam experience
- LGBTQIA+ disability support: respect, privacy and provider choice
- Carer burnout: recognising strain and finding practical support
- Disability representation: Isabella’s response to The Witches
- Living with cerebral palsy: Phin Meere on assumptions
- Fear after a fall: a personal disability perspective
- Melbourne Stage 4 restrictions: a 2020 disability-support archive
- Little wins and disability: finding your own pace
- COVID-19 and disability: reading a historical resource safely
- Disability inclusion: looking beyond wants and needs
- Managing stress: everyday options and when to seek help
- Disability advocates: voices highlighted in the 2019 archive
- Positive mindset and disability: ideas with room for real barriers
- Spinal cord injury and being heard: Anne’s hospital account
- Parent support groups: connection for families of disabled children
- NDIS participant rights: choice, information and complaints
- Parenting with serious illness: support for daily family life
- Autism, gender diversity and respect across communities
- Disability and sexuality education: a historical event guide
- How to Advocate for a Loved One Without Taking Over
- Explaining a child’s diagnosis to siblings: family conversations
- NDIS self-direction: build support around your own priorities
- Pets and disability: Margot’s companionship story
- Autism-friendly haircuts: sensory adjustments and choice
- Disability rights: seeing the person and removing barriers
- Disability support groups: peer experience and decisions
- Visible and invisible mental illness: Monica’s perspective
- Disenfranchised grief: recognising loss and accessible support
- Disability support and everyday choice: needs, wants and late nights
- Family-carer advocacy: Rachel and Emily’s experience
- Wheelchair use and driving assessment: Jo’s licence experience
- NDIS and the horse whisperer: Sam Connor’s media critique
- Disability peer support: making room beyond the crisis
- Life with a prosthetic limb: Amy’s amputee experience
- Sibling relationships and care: choose words and boundaries together
- Disability peer support: share experience and keep your choices
- Unsolicited health advice: setting boundaries with others
- Disability co-design: Sam Connor’s digital project experience
- Invisible disability and social effort: an anonymous account
- Disability identity and difference: making space for change
- Living with absence seizures: Freya’s personal account
- Bourke Street 2017: a historical mental-health commentary
- Disability and sexuality: learning from the SexED Up Expo
- Disability inclusion: belonging without proving your worth
- Difficult conversations about disability: an inclusion perspective
- Advocating for a child’s diagnosis: Alani’s family story
- Reporting abuse in disability services: speaking up safely
- Living with epilepsy and finding purpose: Lesley’s account
- Disability, death and grief: Tristram’s reflection
- Disability and dating: Mark’s story of connection and confidence
- Disability, vulnerability and the right to choose
- Disability complaints in Victoria: choose the right pathway
- Disability, intimacy and the conversations we avoid
- Mental resilience and wellbeing: support without blame
- Disability and rejection: a personal reflection
- Wheelchair access and belonging: an ice-skating experience
- LGBTIQA+ disability inclusion: equal rights and belonging
- Understanding an autism diagnosis: an anonymous personal account
- Disability identity: a personal view of ordinary life
- Neighbour support and disability: asking for help on your terms
- Self-direction and disability: making your own decisions
- Acquired disability and identity: one person’s reflection
- Disability, masturbation and personal privacy
- Independence and accepting help: Jo’s perspective on support
- Meaningful choice: information, support and decisions
- Disability and sexuality: making space for a private conversation
- Living with MS: Teisha’s account of change and connection
- Disability representation: beyond charity and superhuman stories
- Disability, beauty and personal style: Emma’s perspective
- Fatigue after stroke: Emma’s experience of daily life
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