The Family Voices Podcast

In this episode, our host Simone Dudley talks with Dr Megan Hosken on raising concerns that families may have about their child’s health and development. Dr Hosken provides tips and insights on ways to support families achieve the outcomes they’re seeking when visiting a general practitioner (GP) and other health professionals. These recommendations will help speed the process of making referrals for assessment and lead to accessing important services and supports.  Families and professionals will benefit from hearing Dr Hosken talk about the importance of building rapport through a family centred and collaborative approach.

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In this episode our host Simone Dudley talks with Lucy about how the experience of living in a rural community shaped her role in supporting her son, Jake. Lucy shares her story of how her family invested in services for Jake and how she is now a key contributor to his and the community’s support needs. Lucy uses the quote, “the strength of the wolf is in the pack” when describing the opportunities made available by living in an inclusive community.

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In an effort to continually improve, we are asking our community for feedback on the podcast via this short survey. Please share your thoughts with us :)

In this episode, Melo shares his story about parental agency as he talks with our host, Simone Dudley. Melo stresses never to underestimate the importance of a parent’s influence on their child’s development, as experienced with his own daughter.

Listen to Melo as he defines hope as having a goal, believing you can make a difference, and having a pathway to follow. This as well as the benefit that comes from peers sharing their stories truly highlights that parents are a rich resource for one another, for their lived experience incorporates deeper meaning to any message they deliver, and it was this that helped guide Melo back into the driver’s seat. This led Melo to realise – if you believe it to be possible, you begin to see possibilities.

Learn more about the Envisage program mentioned in the episode >>

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www.eciavic.org.au

In an effort to continually improve, we are asking our community for feedback on the podcast via this short survey. Please share your thoughts with us :)

In this episode Ciara talks with our host, Simone Dudley, about the importance of building knowledge and finding your voice. Ciara describes how gaining an understanding of best practice empowered her and her husband to find and advocate for the right supports for their son. This, alongside firsthand experience, led them to establish a peer support group for parents and carers of children on the spectrum. Ciara reminds us that with the right information and supports parents and carers are better equipped to make decisions that lead to better outcomes for them and their children. 

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In an effort to continually improve, we are asking our community for feedback on the podcast via this short survey. Please share your thoughts with us :)

In this episode our host Simone Dudley, talks with Kara about her family and work.  Kara is a mum and researcher from Cincinnati, who studies parenting with disabilities. Kara and her husband are both disabled parents of three children with and without disabilities. Listen to Kara as she shares insights into how her family creates a culture that celebrates disability and how she advocates and builds support for people with disabilities through inclusive practices.

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www.eciavic.org.au

In an effort to continually improve, we are asking our community for feedback on the podcast via this short survey. Please share your thoughts with us :)

In this episode, we hear from Falak, a mother, wife and research and evaluation manager at Rare Voices Australia (RVA). Falak talks with our host, Simone Dudley about her children, two of whom have rare diseases and how her lived experience has deepened her professional role at RVA.

In this conversation, Falak helps to remind us of the importance of trusting our instincts as we continually build our capacity. She also describes the power of gratitude and how giving back to communities that supported her and her family, created a sense of belonging and purpose.

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www.rarevoices.org.au

www.heartkids.org.au

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In this episode, our host Simone Dudley talks with Cassie (Emily’s mum) about her experience with early supports and pioneering the NDIS. Cassie talks about the need for professionals to recognise the strengths of children and work from these when developing goals with the family.

Goals for Cassie and her family needed to reflect the values they held strong for Emily. These included having the same opportunities and experiences that Emily’s siblings had, and being and belonging in her everyday life and community.

These align so well with the principles of family-centred and strengths-based practice, and inclusive approaches as outlined in the National Early Childhood Intervention Best Practice Guidelines. Cassie provides great insights for families who are starting their journey and for professionals to learn from.

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In this episode we are joined again by Leanne (Angus’s mum). This time, Leanne talks with our host Simone Dudley about her personal story of being identified 10 years after her son as autistic and ADHD. Leanne describes how the process of being identified has really helped with understanding herself and with the way she supports her son.

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In this episode, our host Simone Dudley talks with Leanne about what life was like living in an extremely remote location in Australia, while navigating therapy supports and education for her son, Angus. In this remarkable story, hear how Leanne made the most of her family’s circumstance while achieving Angus’s goals through telehealth and home education.

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We would like to welcome Simone Dudley as the new Family Voices Podcast host.

In this episode, our host Trish McIvor talks with Dee, Emma's mum and co-founder of Little Stroke Warriors Australia. Dee shares her story about co-founding Little Stroke Warriors after Emma was diagnosed as having a stroke while in utero. Dee talks about how her own experience has forged the need for improved resources and treatment of paediatric childhood stroke and how this is coming to fruition. She also shares personal insights and on how to be the best support for your child.