Belle talks to Sarah Langston, Founder and President of the Australian Neurodivergent Parents Association (ANPA), about the harms of proposed diversion for autistic children to Thriving Kids, the National Day of Action (May 9th) against the NDIS cuts, and how people can get involved in advocacy protecting the NDIS.

Belle talks to Sarah Langston, Founder and President of the Australian Neurodivergent Parents Association (ANPA), about the harms of proposed diversion for autistic children to Thriving Kids, the National Day of Action (May 9th) against the NDIS cuts, and how people can get involved in advocacy protecting the NDIS.

Belle talks to Sarah Langston, Founder and President of the Australian Neurodivergent Parents Association (ANPA), about the harms of proposed diversion for autistic children to Thriving Kids, the National Day of Action (May 9th) against the NDIS cuts, and how people can get involved in advocacy protecting the NDIS.

Belle chats with Lucinda Crimson, a Perth (Boorloo) based visual artist about having Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) & innovatie ways of adapting art practices for accessibility. We discuss Post-exertional Malaise (PEM) & difficulties navigating healthcare, preventing deterioration into Very Severe M.E. with COVID precautions like masking, and her upcoming exhibition opening June 27th. Stay tuned for the virtual event. For more info: https://www.lucindacrimson.com/

Belle chats with Lucinda Crimson, a Perth (Boorloo) based visual artist about having Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) & innovatie ways of adapting art practices for accessibility. We discuss Post-exertional Malaise (PEM) & difficulties navigating healthcare, preventing deterioration into Very Severe M.E. with COVID precautions like masking, and her upcoming exhibition opening June 27th. Stay tuned for the virtual event. For more info: https://www.lucindacrimson.com/

Belle chats with Lucinda Crimson, a Perth (Boorloo) based visual artist about having Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) & innovatie ways of adapting art practices for accessibility. We discuss Post-exertional Malaise (PEM) & difficulties navigating healthcare, preventing deterioration into Very Severe M.E. with COVID precautions like masking, and her upcoming exhibition opening June 27th. Stay tuned for the virtual event. For more info: https://www.lucindacrimson.com/

Belle chats with Lucinda Crimson, a Perth (Boorloo) based visual artist about having Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) & innovatie ways of adapting art practices for accessibility. We discuss Post-exertional Malaise (PEM) & difficulties navigating healthcare, preventing deterioration into Very Severe M.E. with COVID precautions like masking, and her upcoming exhibition opening June 27th. Stay tuned for the virtual event. For more info: https://www.lucindacrimson.com/

Belle chats with Lucinda Crimson, a Perth (Boorloo) based visual artist about having Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) & innovatie ways of adapting art practices for accessibility. We discuss Post-exertional Malaise (PEM) & difficulties navigating healthcare, preventing deterioration into Very Severe M.E. with COVID precautions like masking, and her upcoming exhibition opening June 27th. Stay tuned for the virtual event. For more info: https://www.lucindacrimson.com/

Belle chats with Lucinda Crimson, a Perth (Boorloo) based visual artist about having Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) & innovatie ways of adapting art practices for accessibility. We discuss Post-exertional Malaise (PEM) & difficulties navigating healthcare, preventing deterioration into Very Severe M.E. with COVID precautions like masking, and her upcoming exhibition opening June 27th. Stay tuned for the virtual event. For more info: https://www.lucindacrimson.com/

Belle speaks to Dr Georgia Van Toorn (Senior Lecturer at the School of Social Sciences UNSW), about the development, implementation and impacts of computer generated assessment tools for NDIS and aged care. She highlighted instances where needs are incorrectly assessed when standardised, and concerns around particularly impacted community groups such as people with complex or invisible disabilities.