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Tony Payne: Welcome to the third and final episode of our special Centre for

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Christian Living podcast series on "Neurodivergence and the Christian life".

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I'm Tony Payne, the Director of the Centre for Christian Living.

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It's great to have you with us again.

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I do hope that you've had a chance to listen to episodes 1 and 2, and let me

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recommend that you do so before you listen to this episode, if that's at all possible.

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In those first two episodes, we set the scene, interrogated the question that we're asking

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and examining, and also looked at the Bible and its theology and what it has to tell us.

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And in this final episode, we'll be turning to think more deliberately and more practically about neurodivergence and the Christian life.

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And so to Part 3 of our three-part series on "Neurodivergence and the Christian life".

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In case you haven't listened to episodes 1 and 2, or in case your memory needs a bit of a refreshing, here's a quick recap of the story so far.

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In episode 1, we interrogated the issue of neurodivergence.

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We listened to the stories of neurodivergent people, parents of neurodivergent kids, gospel

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ministers who are neurodivergent who are coming to terms with what that means for their ministry.

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And we also pulled back and thought more broadly medically, culturally, socially about the nature of neurodivergence

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as a real thing in our culture and in our lives, and the different perspectives that people bring to it.

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And so, episode 1 was very much a matter of interrogating and understanding this issue, and clarifying what the

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questions were that we have about neurodivergence in our lives, especially as Christians and in our churches.

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In episode 2, we turned to the Bible to see what God, the creator of all of us and the

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revealer of the truth about our world—what he has to say about this important question.

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We looked at four important biblical and theological themes, and saw that even though the Bible doesn't mention neurodivergence

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as a subject explicitly, it has a lot to teach us about the nature of ourselves as human beings, as God's creations,

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as recipients of God's grace and kindness, and as recipients too of his Holy Spirit, who draws us together in churches.

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And so, in this final episode, we come back to neurodivergence itself.

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We come back to the experience of neurodivergent people and to the questions that we have

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about how neurodivergence affects our lives and our families and our churches as Christians.

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And perhaps the first thing we should notice is that with the theological framework of the Bible in mind,

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we come back to think about neurodivergence with fresh eyes—with a renewed and transformed mind, with

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a different framework for thinking about neurodivergence than the frameworks that the world provides.

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There are two main frameworks that the world uses to think about neurodivergence.

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They both have their strengths.

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But they both are inadequate on their own terms.

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One of them is I guess you could call the medical model of understanding neurodivergence.

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That is, it sees neurodivergence as a disorder or a disability that is to be understood medically,

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scientifically, and to be treated and cured and alleviated through various medical means.

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Now, this is a valid and worthwhile perspective, and has important things to say.

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But most neurodivergent people would say that it's not an adequate way of describing their experience or describing what neurodivergence is—to see

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it entirely in negative terms as disorder and disability, as a divergence from the norm, as something that is somehow not normal and not healthy.

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As we saw often in episode 1, there are many strengths and positives to do with being

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neurodivergent, both for neurodivergent people themselves and within families and within churches.

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To see it entirely negatively—entirely as a disorder—doesn't seem to do it justice.

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On the other hand, the second main framework that's used for thinking about neurodivergence in our culture is

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more of a political lens or a cultural lens that sees neurodivergence not as a disorder or as a disability.

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In fact, that language is studiously avoided.

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Instead, it sees it as a social phenomenon—as a matter of human rights and political power—in which one

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group, the majority group, the majority social matrix, has marginalised and mistreated another group—othered

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them, excluded them—and the problem really is one of access and politics and power and understanding.

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Now this second framework also is valid, and says something very real and true about the nature of the

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power dynamics of our society and the mistreatment and alienation that many neurodivergent people feel.

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However, it also is inadequate, because it doesn't have the resources to speak really honestly and

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straightforwardly about the negatives—about the problems and dysfunctions of neurodivergent life.

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There's almost an overly positive kind of euphemistic reframing of neurodivergence

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as not being in any sense disordered or dysfunctional, but simply as being different.

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The great thing about listening to what God says about us and our world is that it allows us to speak the truth about us and our world.

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In this case, it allows us to recognise the positives of the neurodivergent experience and what's good about God creating all of us as

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different people with different strengths, while also being clear-eyed and honest about the dysfunctions and problems of life in a fallen world.

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In episode 2, we heard the testimony of Laura about how Psalm 139 speaks to her of the goodness of herself and her own body as God's creation.

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Laura: One of my favorite Psalms, Psalm 139:13-14, says, "For you formed my inward parts.

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You knitted me together in my mother's womb.

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I praise you for I'm fearfully and wonderfully made.

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Wonderful are your works.

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My soul knows it very well." And I just find that a great comfort—that God created me intentionally and that he cares about every part.

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Tony Payne: The Bible celebrates and praises God for the multifaceted diversity of his good creation—of

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all the different strengths and abilities and characteristics that he gives to each one of us.

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However, the Bible is also very clear-eyed and honest about what is fallen and dysfunctional and

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disordered in our world, including all of us, whether we are classed as neurotypical or neurodivergent.

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So neurotypical people have a great many strengths and abilities of an incredibly diverse nature, and also a great

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variety of dysfunctions and disorders and disabilities in their lives—brokenness in their lives of many different kinds.

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And so, to say that neurodivergent people also have a great variety of strengths and abilities, and also their own particular dysfunctions and

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disorders, is simply to say that we're all subject to the judgement and effects of the Fall and of the continuing effects of sin in the world.

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Christian theology gives us a framework to say both of these things honestly and with grace.

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And speaking of grace, that brings us to a second main way we can come back to neurodivergence with fresh

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eyes, with a transformed mind, because the gospel helps us to understand ourselves as recipients of grace.

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It reveals the truth about us: that we're all weak and dysfunctional, that we're all sinners,

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that we're all in need of redemption, and that in Christ, we become a new person and a new people.

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And so, my value and my worth is not tied up with what I can achieve or what I can do, nor is it diminished by what I can't do or can't achieve.

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But my value and worth—who I really am—is determined by the fact that God created me and loved me in his Son.

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And so, whether we're neurotypical or neurodivergent, we're not constituted by our ability

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or our lack of abilities, but by the fact that we're a person loved and redeemed in Christ.

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In that sense, Christianity is not a system of merit, and it deeply and profoundly undercuts the meritocracy

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that dominates our world, and that makes neurodivergent people often feel marginalised and alienated.

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The gospel as it's understood and lived out, protects us from both sides of this trap.

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On the one hand, it prevents us from looking down on some neurodivergent people,

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because they can do less than other people or have particular dysfunctions of their own.

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But it also prevents neurodivergent people from thinking that in order to be valuable and

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worthwhile, they have to have some kind of ability or superpower that is valued by other people.

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The gospel and the Holy Spirit lead me to a new life, a life in which I'm already loved and valuable beyond measure because of the love of Christ.

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It sets me free to stop thinking about myself and instead to start focusing on loving others and serving them.

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Alex: I'm a lot happier when I don't make my identity the core thing about autism, like searching inside myself to find the truth.

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That makes me absolutely miserable in the end.

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But when I'm like, "God made me.

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My identity is that I'm his daughter.

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And he made me perfectly and he knows me perfectly.

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And even if no one else gets me today—if everyone misunderstands everything I say—I'm still perfectly known

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and perfectly loved by him." And, like, I think that just gives me a comfort and a help with the loneliness.

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Like, it's still quite hard, feeling sometimes, like, other Christians don't quite understand.

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But we serve a God who does.

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Tony Payne: That was Alex, talking about the profound change in awareness that comes when the gospel of Jesus invades your life—when

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you realise that your old life is over and a new life has begun, a life that is hid with Christ in God, as Paul says in Colossians 3.

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And this profound change of awareness is true for neurotypical and neurodivergent people in exactly the same way, and it leads in

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turn to a new life, a life in which we put to death the evil habits and behaviours of our old selves, and put on a new way of living.

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In this sense, it's very important to say as we think about neurodivergence and the Christian life and what it means

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practically, that practically, it means a great deal the same for a neurotypical person and a neurodivergent person.

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For all of us, it's a life of thanksgiving and of praise, a life of faith and love and

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hope, a life of transformation in our thinking and in our loves and in our actions.

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But there is a particular aspect of the Christian life that neurodivergent people often find particularly challenging.

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What are we to do and what are we to think when some aspect of our neurodivergence—some consequence of the

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particular way our brain is wired—seems to make the Christian life very difficult—seems to sabotage us?

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For example, one of the fruits of the Spirit is self-control.

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What do we do when our whole body seems to prevent us being self-controlled—when we have a meltdown or an implosion or an explosion, in which

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we don't seem to have any control over ourselves whatsoever, and during which we often say or do things that we profoundly regret later on?

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In one of my conversations with Kate Morris, she gave this example of a Christian friend of hers who deals with these issues in this way.

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Kate Morris: I asked one lady who—she works in ministry, she's autistic, she's also ADHD.

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She experiences meltdowns.

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I asked her to explain to me what she sees is the relationship between sin and what's going on in her body.

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And she said to me that—she kind of asked the question, "Is it that because you understand that

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my body has experienced such pressure from being at church or something that it's melting down and

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therefore I'm absolved from all responsibility?" And she said, that's not really how we approach things.

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She suggested that we live in a broken world with broken bodies—with wayward hearts inclined to sin—and we're going to sin.

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And when we sin, we need to apologise.

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We need to say sorry.

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And so, for her, when she has a meltdown, she asks that her family is understanding to her and sees what's been going on in her life.

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But she will say sorry for what she's done and work on rebuilding those relationships and hearing the family's experiences in that.

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And she's also working with an occupational therapist and a psychologist in order to bring down those triggers—in order to identify when she's

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building up to a meltdown, which is a loving approach, so that she can actually work to not getting to the meltdown stage quite so easily.

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Tony Payne: What's striking and impressive about this lady's response to her own

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meltdowns and to the effects of those meltdowns is just how thoroughly Christian it is.

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That is, it recognises what the New Testament also recognises: that our bodies, our flesh, the presence of sin living within us,

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will often lead us to do things that, really, in our truer selves, we don't want to do—that sense of "I do not do the good that I

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wish I would do, and I do the very thing I wish I wouldn't do" that's there in Romans 7 and it's certainly also there in Galatians 5.

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The Christian life is a constant battle between the bad habits and actions of our bodies—our flesh,

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our former selves, our old selves, our old habits, what our bodies do almost on their own sometimes, it

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seems—and the new life that's been planted within us—the new mind, the new heart that has a new set of loves.

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And the lady that Kate talks about responds in a way that we should respond to all sin in our lives: she laments the

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wrong things that she's done; she takes responsibility for what she's done; she apologises and seeks to make redress

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where she can; she shows herself and others some grace; she remembers that God forgives, and she forgives herself for

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the way that her body has led her astray; and she also seeks to learn something and to grow through the experience.

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What was it that led to that loss of control?

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What triggers or factors in my life led me to that point where I did lose control and behaved poorly?

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This is where a diagnosis of neurodivergence—of ADHD or autism—can actually be quite helpful in living the Christian life.

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And many of the neurodivergent people we spoke to testified to this—that it gave them an understanding of themselves

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and of why they reacted in certain ways in certain situations that actually helped them to manage their lives and their

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reactions—to be thoughtful and proactive, to avoid the kinds of circumstances or triggers that often led to difficulties.

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In all of this, it's not as if any of us, neurotypical or neurodivergent, will reach perfection in this life.

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The key is to continue to make progress.

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"Let everyone see your progress," Paul said to Timothy in his letter to him, as he set an example for the saints in Ephesus.

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Start with where you are—with your own particular strengths and weaknesses—and let

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everyone see your progress, no matter how small and faltering that progress might be.

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Put off the old and put on the new.

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Well, let's move on from the challenges of the Christian life and how it's lived to the challenges of parenting.

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How does a biblical and theological lens help us understand and respond to the particular challenges of parenting neurodivergent kids?

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Callum was one of the parents we interviewed for this project, and he had this to say.

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Calum: I don't think I've asked God "Why?" more in my life than I have since becoming a parent and understanding more about my boys' needs.

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I think for me, as a Christian growing up and as a Christian looking forward to parenthood, I had these visions

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and expectations about serving in ministry alongside my kids, bringing my kids along to holiday clubs and serving

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with them, going to church with them while serving in kids programs, having a vision of ministry together.

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As someone who'd done a lot of kids' ministry, I was looking forward to that.

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And I wonder why the children that God's blessed me with aren't children for

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whom that's going to be a positive environment to serve in ministry together.

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They're not people whose sensory ability says, "Yeah, I can be around lots of big

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groups of people." That's just not a space that's going to be conducive for them.

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And my selfishness driving me to say, "This is how I thought God was going to drive my life."

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But instead, having the humility to say, "Well, no, God's given me these great gifts of children.

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As a parent of them, I'm going to serve where he's placed me." And I think, I

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mean, I'm what, nine plus years into being a parent and still working that out.

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Tony Payne: Understanding his children's neurodivergence as both gift and challenge—as positive and wonderful in certain circumstances, and

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incredibly difficult in others—this was not only Callum's experience, but the testimony of many parents we spoke to of neurodivergent kids.

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Among them was Kate Morris, and Kate had some really helpful things to say, not only about the practicalities of raising and

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dealing with neurodivergent kids, but also of the whole new perspective that the gospel gives to parenting a neurodivergent family.

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Kate Morris: I think for me as a parent, the biggest thing is it reminds me that I'm a person who needs grace.

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I'm sinful.

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I'm broken.

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I'm inclined to serve myself more than others.

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I'm inclined to look at my capacity as the place where I'm going to save myself.

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I'm inclined to be self-sufficient and autonomous.

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I think I see my sinfulness in being a parent, and I know that Jesus is the solution for my brokenness—for my evil heart—and I

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know that he is working to mature me—with the work of the Holy Spirit, is changing me, and I see that as I parent my children.

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I think it gives me a really important understanding of who my children are as well.

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They're my children.

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But they're God's children: even more than that, they're God's children.

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And I can sit knowing that their futures are in the hands of the one who made the universe—the hands

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of the one who has given us salvation and redemption—and I can entrust them to the good Father.

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When I see I'm not a good mother, I know I can entrust them to him.

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And I think too, it reminds me that what I want for my children isn't to look like everyone else.

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I want them to look like Jesus, and that's actually my aim.

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And I know that they're not saved through me.

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No matter how good a parent or how bad a parent I am, I'm not going to win them salvation or lose them salvation.

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I look to Jesus for everything they need.

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And that's remarkably freeing.

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I think it gives a good perspective, too, on the times—there are times when the challenges, they just

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bring such grief, whether because the whole family is suffering or whether one of my children is suffering.

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There is grief in this and anguish and pain, and I know that together, we can look to God for comfort.

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And I know that he promises to give us wisdom when we ask for wisdom.

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And so, even in those times of great difficulty, I know that we're safe and I know that we're not falling outside of God's plan even in those times.

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Tony Payne: The gospel of grace does give us a new perspective on everything in life, including raising our kids and raising neurodivergent kids.

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But it's not just a new perspective; there are still practical challenges—the challenges of

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disciplining and raising these particular kids with their particular strengths and weaknesses.

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Those of us who are parents will testify that this is the case in every family—that it's extraordinary how different our kids can be from

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one another and how there needs to be different approaches to different children, depending on their particular individual characteristics.

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And this is the case with neurodivergent kids, perhaps even more so.

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Here's Kate again, reflecting on the complications of disciplining neurodivergent children.

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Kate Morris: It is complicated, because with children who are neurodivergent, a lot of them will experience complications and triggers and

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difficulties—particularly outside the home, but also in the home—that will mean that they have a pressure build-up that can be quite complicated.

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So I think one of the most challenging aspects of parenting a neurodivergent child

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is if they experience meltdowns or shutdowns—particularly meltdowns can be complex.

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So meltdowns: unfortunately, we use that term interchangeably with tantrums, and it's not a tantrum.

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A tantrum is where a child wants a cookie and you can end the tantrum by giving them a cookie.

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They want something; if they don't get it, then they will kick and scream.

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A meltdown is quite different, actually.

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We understand now that a meltdown is a brain explosion.

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It's closer to a dam break.

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It's closer to a nuclear meltdown or something like that.

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It's something where the pressure has built to the point that they can no longer hold it in.

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So a lot of parents will notice these meltdowns happen in the car as they're

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heading home from something, where the child has held it in, or when they get home.

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And it's really hard, because this is the moment where a family would love to just relax together.

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But for some people, relaxing means releasing a lot of tension and build-up.

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So I think there are some stages of our approach to meltdowns, and the end point, the last stage, is actually where the discipline happens, I think.

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But I'm interested to hear what other parents say on this as well.

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So there are three stages of a meltdown, but I'm adding a fourth onto the end.

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The first stage is where the pressure has been building, and you can often see in your child, or perhaps

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they can identify in themselves, that they have experienced so many triggers that the pressure is building.

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So for some children or adults, it will come across as sweating, heart palpitations, jitteriness, perhaps an inability to sit still.

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They might rock back and forwards.

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They might lie on the ground and cover their ears and their eyes.

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And if you can notice—as a parent, if we can notice these things in our child and identify some

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ways to comfort them, then sometimes you can actually release the pressure without a meltdown.

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And so a loving thing to do as a parent is actually to be on the lookout for these and to be on the lookout for ways to help them.

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And so that can be a cooperative approach with your child at times where they're not experiencing this pressure build-up.

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"What would you like me to do when you're experiencing that? How can I identify that in you? How can you communicate to me that you're

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experiencing that?" There can be things that will calm them down using the various senses that parents can figure out with their child.

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But if it can't be stopped, then you're in the stage of the meltdown, and it's

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really important for parents to understand, as much as we might want to say, "Stop.

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Stop.

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Don't do it.

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You're being naughty.

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You're going to have a punishment later," or something like this, that is absolutely the opposite of what a child needs.

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And so, again, it's a collaborative approach.

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What does your child want in these times?

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For many, they want to have co-regulation.

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So whether that's you sitting in the same room, breathing loudly and saying things like, "This will end.

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I understand you're feeling distraught.

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I understand you're upset.

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This will end." Or perhaps, "I love you.

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I'm never going to stop loving you.

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God's never going to stop loving you.

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I'm right here." And in order to do this safely, it might mean removing siblings.

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It might mean removing unsafe things around them.

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And before meltdowns, we can practice these things with a child, teaching them through cushions, not objects.

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"Punch the couch; don't punch yourself. Don't pull out your hair; instead, pull on the curtains." And we can work out replacement behaviours.

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And then when they're coming down out of the meltdown, it can be tempting to jump in with the discipline right there, right?

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"You did this and this and this. Here's the consequence." But you risk going back into the meltdown.

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The pressure hasn't completely come down yet.

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And so in that moment, a loving parenting thing to do is to calm with them, perhaps hold them if they want.

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A lot of children don't want to be held still.

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Perhaps reading a story, hearing an audio book together, having the air

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conditioning on, weighted blankets—whatever the child and you have figured out.

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And then it's after this has really ended that you can start to think about what the next step can be.

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And I would suggest too, that for parents, you need to make sure that you've

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calmed down too, 'cause these can be massively difficult moments for parents.

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And it's loving to speak to our children and help them to understand the impacts of what they have done.

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Tony Payne: There's so much more to be said on this subject, of course, and Kate's Substack, which is called "An extraordinary normal"—we'll put the

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details of that in the show notes—is a great place to start in having that conversation and in finding your way to other resources on this topic.

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But let's move on to the third and final practical area we want to consider, and that's neurodivergence and church life.

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Church is simultaneously wonderful and difficult for many neurodivergent adults and kids.

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It's a place of grace and gospel, where we meet the God who explains us to ourselves.

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But churches can also be very unwelcoming places, unfortunately, for neurodivergent adults and kids, often without meaning to or realising it.

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The lights, the sounds, the sheer number of people, the constant chatter, having to relate to lots of different people, one after the other.

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Church can be a really challenging environment for neurodivergent adults and kids.

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And what is most often needed is simply some understanding.

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Here's Alex's experience.

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Alex: Yeah.

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Actually recently, like, I went to a doctor's appointment, and I was like, "Oh, sorry, I don't—I'm not in

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a head space where I can process eye contact right now. Do you mind if I just keep my sunnies on?" And he's

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like, "Oh, no worries at all. Do you want me to dim the lights?" And he just dimmed the lights slightly.

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And that experience of that doctor's appointment was the best doctor's appointment I've ever had in my life.

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And yet, the thing that he did was, like, so small, but the amount of difference it made was, like, crazy.

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And even, like, the other day in my Bible study, I was saying to the girls in my Bible study, like,

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"What do you think I should do on a day where I just want to, like, rock backwards and forwards?

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My brain can't process something to the level, but the amount that I need to stim to be able to

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process the environment around me is really intense." And they're like, "No, still come to church.

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But maybe just sit in the foyer where you can still hear the message." But, like, they're encouraging me: it is okay

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to do something that will probably—other people might not understand it at first, because they don't see me do that,

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because I wait until I get home and then I do that, and by that point, I'm so overloaded that I feel awful and horrible.

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Whereas, last week, I did that: I just rocked backwards and forwards the whole time.

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And at the end of doing that, afterwards, I was in a point where my brain, for

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once after church, I could actually process conversations we were having properly.

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Like, I took off my glasses.

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I had really encouraging conversations.

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And I went home and felt good for once.

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And usually, my experience of church is by that point, I feel really, really awful.

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And it's not because anything has gone wrong; it's because my brain gets to a point where there's so much stimulation that I can't process it.

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And I will stim, but I'll do mini stims that are more, like, probably socially acceptable, because I know rocking

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backwards and forwards will make me look like—to some people, they'll be, like, "Oh, she never does that. She looks

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like she's having a mental breakdown", because neurotypical people do that when they're very upset, whereas autistic

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people just do that when they need to process something—can do it when they're upset, can do it when they're happy.

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So yeah, it was really nice to be given that permission that no, it's okay to be yourself at church.

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You are welcome, and the level that you'll distract other people, it might distract someone, but it's okay if that's what you need.

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Like, yeah.

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Tony Payne: When church is working well—when we function as a body where all the parts do seek

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the benefit of the other parts and contribute each in their own way—it can be a beautiful thing.

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Here's Sarah talking about how small group studies—small group Bible studies—can be a really

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encouraging place for her as an autistic person, especially if they're managed with a bit of care.

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Sarah: So I find that I really benefit from studying the Bible in a small group.

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For example, having that consistent structure, like, whatever method you want to follow, whether it's the SOAP method or the

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five Rs from the Uncover series, or you're working through some study guide for the Book of John, or whatever it happens to be.

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Just having that consistency is helpful.

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I also find—this might be a contentious issue, but some autistic people withdraw and don't really participate.

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But then there's the other extreme where they kind of dominate the whole conversation.

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And I'm probably just as bad, but when there's more than one autistic person in the group, and we're all talking and butting in

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over each other and then going on tangents, it's really important, I find, to have a strong moderator who just gently pulls the

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group back and goes, "Oh, good points, but maybe we should get back to the topic, 'cause we don't want to be here all night."

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So I actually find, 'cause I read a book years ago called Making Small Groups Work by Cloud and Townsend,

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and they made a point that the poorer the social skills in the group, the more need for structure.

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So if you've got six neurotypical people who have great social skills, you probably don't need as much structure.

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But when you have autistic people in the group, that structure and that moderator in the middle—that facilitator who just

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gently redirects the conversation back—I find is really helpful and it helps people feel safe also, 'cause with autism,

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we can accidentally make a comment that's hurtful to someone and not realise how it came across with the tone or whatever.

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So just having someone to be in the middle—preferably a neurotypical person, I'm going to

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say—who can just smooth over those bumps and just make sure the other person is feeling okay.

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Not attack the person who said it, but just, you know, that—the social skills that we sometimes lack.

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So yeah, I find that's helpful.

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Tony Payne: So you might be a church pastor or a church member, and you are thinking at this point, "Well, yes, this all sounds great.

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We do need to address this question.

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This is something we haven't thought about nearly enough.

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What can we do?

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Where should we start?

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What sort of action plan should we put in place?" In one of the conversations I had with Kate Morris,

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I asked her almost exactly this question as someone who's navigated this in a number of contexts.

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And this was her answer.

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Kate Morris: The approach needs to be the approach that we have to everyone who comes into our midst.

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We need to be loving like Jesus loves, asking questions of people, hearing their experience without jumping into put them in these boxes that we

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love to put people into, without jumping to fix the problem, without comparing, beginning with believing and asking what supports they might need,

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offering supports that you might be able to offer, and working out how this family or this person can be in our community, serving alongside us,

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working with us as a community, rather than segregating people out as separate people who we support, understanding that we're all part of this body.

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I think some practical things on the ground: I think most churches would love to have a checklist where I write down 50 things, and as long

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as they can tick off these 50 things, then they know they've got a church that's going to welcome neurodivergent people and we're done.

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And isn't it wonderful that we don't have that checklist?

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Because if we did, I might put something on that like, "Most neurodivergent people with sensory sensitivities find fluorescent

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lights very overstimulating, and for some, actually painful, so therefore change your lights to LEDs." Churches can do that.

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They can tick that off.

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And then they think, "Well, I'm done on lighting." But for another person, those lights are bright, or the LED has a

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particular flick to it that they can't stand, or how come lights are on everywhere and there's no dark place for me?

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And so, we don't want a tick or cross thing.

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It has to be that we approach this with understanding.

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And I think a way to do that is for all of us to commit to learning what we can in this area so that we can ask things.

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"How's the lighting for you?" And not be surprised when someone says, "Did you notice

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that in the kids' church room you can hear the electricity in the walls?" "Oh, can you?

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Great.

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Well, let's work out what we're going to do about that."

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I think it's hard to, when there will be families who know that they need support, know that church is really hard and overstimulating,

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and don't necessarily know what to ask for, and that's where, if we've got some experience in this, if we've got some understanding

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in this, we might be able to gently begin, "Well, shall we try this? Shall we try that? For some families, this works."

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I think the underlying principle of being curious—I think that's important—but I

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think also being prepared to be flexible on things that we might hold so dear to us.

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We have a lot of things in our church culture here in Australia that we think

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is natural or that is biblical, and it's not necessarily natural or biblical.

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We can actually let them go.

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Can someone enter from a side door and not say hello to anyone and sit down?

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Would we allow that?

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Can we be flexible enough for that?

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We like our churches to fill from the front: would we be flexible enough for a family or a person to sit in

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the exact same seat every single week, so that they don't have to reprocess angles and lighting and so on?

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Would we be flexible enough to take one of our rooms in our church building

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and use it as a sensory space that can be quiet if someone needs to recover?

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Can we be flexible with our kids' church programs in order to allow a child to spend some time in a tent or on a rug or something?

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Will we put people in front of programs and in front of places?

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And I think if we have these sort of underlying our approach to people, I think it will help in

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welcoming families into our church and helping them to know that they belong and to feel supported.

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Tony Payne: Well, that's a wonderful answer.

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It seems to me, and a fitting place, perhaps, to draw this final episode towards a close.

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It's not really so surprising, is it, that the basic practical response to neurodivergence in our lives and homes and churches is

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some form or other of Christ-like love that springs from the gospel of grace—in how we understand ourselves and live the Christian

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life, no matter what our particular strengths or weaknesses or dysfunctions might be; in how we parent our children, no matter what

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their individual strengths and weaknesses and dysfunctions might be; and in how we love and serve one another as church communities.

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At each point, our practical response is founded on the central truths of the gospel—that each of us are God's good though

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tragically fallen and rebellious creatures; that in the gospel of Christ, we're all saved from the judgement of God, saved in the

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same way by his merit and his saving death, not anything we do or anything we contribute, and that the new life we live in Christ

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is a life of faith—being active in love; of thinking about others, rather than ourselves; in putting to death the lingering bad

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behaviour of our old lives; and of loving and welcoming others with all their different needs and contributions in our fellowship.

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There's so much more we could say, of course, about this subject.

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But our hope in this podcast series has been to open up the issue of neurodivergence

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within the Christian community and in the Christian life, not to provide the final word.

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To continue that conversation, we'd love you to get in touch with us and ask your questions and

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make your comments on this podcast series, and I'll tell you how to do that in just a moment.

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But we'd also love you to seek out good resources and conversations, and continue the thought process

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yourselves in various ways, and we'll put some suggested resources and next steps in our show notes.

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But perhaps it's appropriate if we give the final word in this episode in this series to one of the neurodivergent people we spoke to—to Peter.

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Peter: What we want to do is have other Christians to recognise that we are made slightly

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different, even though they can't physically see it—that mentally, inside us we are different.

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Our brains are wired differently.

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And even though we have weaknesses in how we communicate and how we act towards people, we also have enormous strengths.

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And so, try and embrace us not only for our weaknesses, but also for our strengths.

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And I think that's something that Christians should do, and as somebody with Aspergers and as a

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Christian, it's something I ask other Christians to do, and it's something that I do on a regular basis.

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Karen Beilharz: Digital technology like smartphones has revolutionised the way we navigate daily life and the way our whole society functions.

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We have supercomputers in our hands that can answer almost any question instantly and perform many tasks that make life easier.

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Such technology has its downsides, like the explosion of accessibility to pornography and the prevalence of online bullying.

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Even so, our stance as Christians is often something like, "Let's use this technology

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wisely, but not abuse it", as if the technology is simply a neutral instrument.

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But the good things of our world, like technology or money, can become much more than this.

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They can become master teachers that dominate and disciple us.

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In the next Centre for Christian Living biblical ethics workshop, we want to do

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more than share helpful tips on godly smartphone use, although such tips are useful.

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We want to zoom out and consider how technology disciples us—how it profoundly reorders our

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attitudes, operating beliefs and behaviours, not just personally, but on a society-wide level.

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Put your phones on silent and join the conversation on Monday 27th of October 2025 at 7:30 pm.

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You can register and find out more on the Centre for Christian Living website: ccl.moore.edu.au.

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That's ccl.moore.edu.au.

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Tony Payne: Well, thanks for joining us on this episode of the Centre for Christian Living Podcast from Moore College.

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For a whole lot more from the Centre for Christian Living, just head over to the CCL website: that's

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ccl.moore.edu.au, where you'll find a stack of resources, including every past podcast episode all the

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way back to 2017, videos from our live events and articles that we've published through the Centre.

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And while you're there on the website, we also have an opportunity for you to make an

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tax-deductible donation to support the ongoing work of the Centre here at Moore College.

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We'd also love you to subscribe to the podcast and to leave a review so that people can discover our podcast and our other resources.

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And we always love and benefit from receiving your feedback and questions.

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Please get in touch: you can email us at ccl@moore.edu.au.

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Many thanks to Karen Beilharz from the Communications Team here at Moore College for all her work in transcribing and

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editing and producing this podcast; to James West for the music; and to you, dear listeners, for joining us each week.

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Thank you for listening.

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I'm Tony Payne.

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'Bye for now.

