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The SEND Mum Club

Podcast af The SEND Mum Club

engelsk

Familie

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The SEND Mum Club is the parenting podcast with a difference. Made specifically for parents of children with all kinds of additional needs and disabilities. It's a place to share the joys and challenges of raising children with all kinds of SEND, by having raw, honest conversations, designed to make you feel seen and heard on a journey none of us expected to be on.

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48 episoder

episode 45: Christian Laing: Growing Up With A Brother With Down Syndrome, Setting Up Stand Out Socks & Why There’s Still Such A Long Way To Go cover

45: Christian Laing: Growing Up With A Brother With Down Syndrome, Setting Up Stand Out Socks & Why There’s Still Such A Long Way To Go

In this episode I talk to Christian Laing – co-founder of Stand Out Socks – about what life was like growing up with a sibling with Down syndrome. We discuss how that impacted Christian’s upbringing, how involved Ross was (and is) with Christian’s friends, and what Christian’s thoughts are now looking back as an adult.   Christian, Ross & Christian’s partner Natalie founded Stand Out Socks (you may have seen them on Dragon’s Den) because Ross was struggling to find paid employment. Christian talks about how many people with additional needs end up working for free, or even paying to work and why it’s so important that changes. All the people that work at Stand Out Socks have Down syndrome and all of them are paid for every hour they work. I was absolutely shocked to learn how rare that is.   You can shop the socks and find out more at www.standoutsocks.co.uk [http://www.standoutsocks.co.uk] and follow them on Instagram @standoutsocksuk

27. apr. 2026 - 54 min
episode 43: Liz Day: Parenting a Medically Complex Child With a Very Rare Genetic Condition cover

43: Liz Day: Parenting a Medically Complex Child With a Very Rare Genetic Condition

This episode marks a year of The SEND Mum Club podcast. Thank you so much for listening! Liz Day is my guest this week, talking about her 4 year old son Henry who has the CASK gene mutation, an extremely rare genetic condition that affects boys much more severely than girls. We discuss the bleak outcome they were told to expect in terms of life expectancy and how Henry has already proved the doctors wrong. Liz talks about going back to work and how she manages that alongside Henry’s needs. We discuss how hard it is to give over some of Henry’s care to carers and the difficulty in finding peer support when his condition is so rare in boys. Liz mentions the Unique charity as a good resource if you’d like to learn more about Henry’s condition https://rarechromo.org/disorder-guides/ [https://rarechromo.org/disorder-guides/] You can find Liz on Instagram @medical_mumma_kickingcask

23. mar. 2026 - 1 h 4 min
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