『Let's Take Care - Support for Carers of Disabled Children and Young Adults』のカバーアート

Let's Take Care - Support for Carers of Disabled Children and Young Adults

Let's Take Care - Support for Carers of Disabled Children and Young Adults

著者: Jane Holmes and Melissa Paulden
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Melissa and Jane have been caring for their daughters for over 20 years, helping them to lead hugely successful lives. But they've made some mistakes along the way, and learnt a lot. Or, learnt the hard way.

They've been tired, burnt out, broke, ignored, isolated - yet still expected to keep going.


Let's Take Care is their way of helping other carers of disabled children feel less alone - and more equipped to cope with the realities of care that no one talks about.


In each episode they'll talk about the emotional and mental weight of lifelong care - what it's like to fight the system constantly and how to survive practically, emotionally, physically.

They'll be sharing what they wish they knew 20 years ago ... and hoping to make you laugh as well.

© 2026 Let's Take Care - Support for Carers of Disabled Children and Young Adults
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  • Let's Take Care - Celebrity Parent Carers and their journeys
    2026/06/04

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    In Episode 11 of Let's Take Care, we explore the growing number of celebrities and public figures who are sharing their experiences of raising disabled children and young people.

    From social media posts to TV interviews and documentaries, these voices are helping to bring SEND family life into the mainstream, raising awareness, challenging stereotypes and helping other parents feel less alone.

    We discuss the impact of this increased visibility, the opportunities it creates for advocacy and change, and whether there is still more to be done to ensure disabled children, young adults and their families are truly represented.

    We also reflect on the much-loved poem Welcome to Holland by Emily Perl Kingsley, recently shared by Jesy Nelson, and ask why it continues to resonate so deeply with parents nearly four decades after it was written.

    Join us for an honest, thoughtful and uplifting conversation about visibility, advocacy, acceptance and the power of sharing our stories.

    https://www.bftf.org.uk/

    Email us at: letstakecare@bftf.org.uk


    #DisabilityAwareness #ChronicIllness #HiddenDisability #SENDParent #AdditionalNeeds #SpecialNeedsParent #DisabilityCommunity #InclusiveFamilies #CarersUK

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    40 分
  • Episode 10: Steve's story - being a neurodivergent Dad to neurodivergent adoptive children
    2026/05/01

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    What's it like to find out you have autism as an adult?

    In this episode Melissa and Jane sit down with Steve, an adoptive dad and charity volunteer, to talk honestly about parenting two teenagers with neurodivergence.

    Steve shares the story of his own autism diagnosis as an adult, and how that helped him support his children.

    We also get into self-care that actually works for neurodivergent adults: reducing the constant mental noise, setting boundaries around socialising, and finding environments where you can thrive. Steve reflects on work, inclusion, and why he sometimes prefers a bit of chaos, plus what he has learned from volunteering with adoption and disability communities where “like recognises like” and families finally feel seen.

    If you know someone parenting through diagnosis, disability, adoption, autism or ADHD, share this conversation with them, and if it helps, please subscribe and leave a review so more carers and dads can find it.


    https://www.bftf.org.uk/

    Email us at: letstakecare@bftf.org.uk


    #DisabilityAwareness #ChronicIllness #HiddenDisability #SENDParent #AdditionalNeeds #SpecialNeedsParent #DisabilityCommunity #InclusiveFamilies #CarersUK

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    40 分
  • Episode 9: Practical tips to help parent carers - before there’s a crisis
    2026/04/01

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    One cancelled care shift can wipe out a whole day.

    Parent carers often seem able to do it all - because they have to, but that can make friends, family, and professionals assume they can cope without them, and because of that, sometimes, people let them down.

    Caring for a child with profound disabilities is not just “busy”. It is a constant mix of medical needs, physical lifting, education battles, and the emotional weight of being the only person who truly knows what “normal” looks like for your child.

    In this episode Melissa and Jane discuss what "help" really looks like when you're mum to a disabled child, and how friends, family and even strangers can lighten the load.

    They talk about why asking for help can feel impossible when your child has complex medical needs, and why respite care can be something you desperately need yet still dread. If you’ve ever felt guilty for needing a break or judged for not taking one, you’re not alone.

    Listen now for real-life tips for supporting parent carers, and a clearer picture of what “showing up” really means.


    Subscribe, share with someone who needs this conversation, and leave us a review with the kind of help you wish people offered more often.

    #ParentCarer #CarerLife #Caregiving #DisabilityAwareness #SpecialNeedsParent #SENDParent #ComplexNeeds #DisabilitySupport #InvisibleLoad #ChronicCare
    #YouAreNotAlone #RealTalk #HonestMotherhood #MentalLoad #CaregiverBurnout #ItsOkayToNotBeOkay #ParentingReality #UnseenStruggles
    #SupportMatters #ShowUp #CommunitySupport #HelpingOthers #BeThere #StrongerTogether #KindnessCounts


    https://www.bftf.org.uk/

    Email us at: letstakecare@bftf.org.uk


    #DisabilityAwareness #ChronicIllness #HiddenDisability #SENDParent #AdditionalNeeds #SpecialNeedsParent #DisabilityCommunity #InclusiveFamilies #CarersUK

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    43 分
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