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The One in a Million Baby

Our lives are full of odds. We buy lottery tickets when the chances of winning are as small as one in 40 million. But when the circumstances are a little different and the odds mean something rare and unusual, like a chromosomal abnormality or a medical condition in our children, we dismiss the much higher odds which can be as high one in 800 because we assume it won’t be us who make up that one. The One in a Million Baby tells the stories of the children and their parents who find themselves as that one in a thousand, or one in ten thousand, or even one in a million position and how they come to cope.
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The One in a Million Baby
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Now displaying: 2018
Apr 23, 2018

Denise Astill is the founder of FACS, an organisation set up to support and raise awareness for Foetal Anti-Convulsant Syndrome. Her twin daughters were born with the funding and qualify for ACC funding. But she knows that many families miss out on this vital funding. 

Mar 8, 2018

Carla McNeil comes to this conversation as a mother, an educator and now a professional advocate for children with dyslexia in her role at Learning Matters. In this episode she talks about what she sees as the key issues in the classroom for teachers and learners when there is a learning difference present. 

Mar 1, 2018

Kerry Hodge and her family were dreading the new school year without the necessary supports for her son, Felix. In this episode she talks about the struggle to get new supports and how she feels lucky, but really it shouldn't be about luck, these kinds of supports should come standard. 

Feb 26, 2018

Paula Tesoriero is New Zealand's Disability Rights Commissioner. In this episode she talks about what she intends to do in the role and how she came to terms with her own disability caused by amniotic band syndrome before she was born. 

Feb 16, 2018

People buy houses in specific zones for the schools they offer their children, but when you have a child with learning disabilities and complex needs in New Zealand, you may have to move entire cities just to get your child an equitable education. This is the story of Tansy Sayers, her son Charlie, and their move from the Wairarapa to Wellington to get Charlie the education he deserved and needed. 

Feb 5, 2018

Beth Armstrong struggled to find equitable education for her daughter Molly. They tried one school after another, and despite some valiant efforts on the part of the schools and teachers, it wasn't until she reached high school, where there was a dedicated unit for students with disabilities and complex needs that Molly started to flourish. 
In this episode Beth tells her journey of trying to find equity for Molly in a system which doesn't give many options. 

Jan 26, 2018

Rebekah Corlett is a fierce advocate for disability rights and equity in education. She does this on behalf of her daughter Sophia, but also on behalf of other children and teens in New Zealand who aren't getting a fair shot in the education system. 

Jan 23, 2018

At 20 weeks pregnant, doctors told Nicole and her husband Ben that something was wrong with their child's brain. When Pierce was born he struggled to breath, and at six weeks he had a tracheostomy.
But it wasn't until Nicole googled facial paralysis when Pierce was 6 months old that they discovered he had Moebius Syndrome. This episode, released for the 24th of January, Moebius Syndrome Awareness Day, tells their story. 

Jan 14, 2018

To kick off this short series on education in New Zealand and the challenges parents, kids, teachers and teacher aides have, we've got Emily Writes, author of the brilliant Rants in the Dark, and fierce advocate for her children. 

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