Autism

  • Nurturing Independence in Your Autistic Child: A Heartfelt Guide

    • by

    Nurturing Independence in Your Autistic Child: A Heartfelt Guide

    Encouraging independence in autistic children often feels like walking a tightrope without a safety net. I’ve stumbled more times than I can count, wondering if I’m pushing too hard—or not enough. In this post, I’ll share what’s helped me support my autistic child’s self-reliance with gentle, practical steps that honor their unique rhythm. You’re not alone in this; let’s explore how to nurture independence, one small victory at a time.

    Encouraging Self-Reliance

    Fostering independence in your child begins with understanding and empathy. Every small win is cause for celebration, as each step forward builds confidence and autonomy.

    Practical Autism Parenting Tips

    When it comes to nurturing independence, consistency is your ally. Start with simple, everyday tasks. You might have your child help with setting the table or picking out their clothes. These are not just chores; they are opportunities to grow.

    Imagine your child choosing their breakfast cereal. It seems small, but it’s huge! It encourages decision-making, which is a cornerstone of independence. And remember, patience is key. There will be spills and mismatched outfits, but these are learning moments that pave the path to greater self-reliance.

    Small Wins and Celebrations

    Celebrate every achievement, no matter how small. Did they tie their shoes for the first time? That’s a big deal! Make a sticker chart or offer high-fives as rewards. These acknowledgments boost their confidence and reinforce positive behavior.

    Create a ritual to mark these victories. Perhaps a favorite snack or a special storytime treat. These celebrations are reminders that progress is happening, even when it feels slow.

    Supporting Autonomy in Daily Life

    Creating a supportive environment is essential for helping your child feel safe and empowered. Structure and routines play a critical role in this journey.

    Creating Routines and Structure

    Routine is comforting. It’s like a roadmap for your child’s day. Start by crafting a simple schedule that includes visual aids. Picture cards can show steps like brushing teeth or putting on pajamas. This visual roadmap helps them understand what to expect next.

    Think of routines as the backbone of your day. They provide stability and lessen anxiety, allowing your child to engage more confidently with their surroundings. Slowly introduce changes to the routine to build flexibility and adaptability.

    Encouraging Decision-Making

    Encourage your child’s autonomy by offering choices. Simple decisions like asking if they want to wear the blue or red shirt empower them. It teaches them to weigh options and make decisions based on their preferences.

    Consider this: The more you let your child decide, the more they’ll understand their own likes and dislikes. This self-awareness is a powerful tool for independence. Remember, it’s okay if they choose the mismatched socks. It’s their choice, and that’s what counts.

    Navigating Challenges Together

    The journey is not without its challenges, but facing them together strengthens your bond and builds resilience.

    Real Stories from Our Autism Family Journey

    My son Adrián once faced a school presentation. The thought of speaking in front of others was daunting for him. We practiced together, turning it into a fun game at home. He delivered his presentation the next day with poise and confidence.

    From this, I learned that preparation and support are key. Being there, cheering them on, and preparing them for what’s to come can turn fear into triumph.

    Finding Humor and Hope in Hard Moments

    Sometimes, laughter truly is the best medicine. When things don’t go as planned, try to find humor in the situation. It can lighten the mood and make the challenges seem less daunting.

    For instance, when Guillermo spilled juice all over his shirt before a big event, we laughed and called it a “fashion statement.” This light-hearted approach made the situation less stressful for both of us.

    Remember, each challenge you face together strengthens your relationship. You’re not alone in this journey. Lean into the community of parents and caregivers who understand and support each other.

    🌟

    Each step you take, every choice you make, and each challenge you navigate brings you and your child closer to a place of confidence and independence. Keep celebrating those victories, no matter how small, and remember—you’re doing an amazing job.

    Check out our books and FREE Resources

  • Explaining Autism to Your Child’s Siblings: A Heartfelt Guide

    • by

    The Question That Broke My Heart (And Opened a Door)

    “Why does Adrián get to stay home from Grandma’s party, but I have to go?”

    My neurotypical 3-year-old niece asked me this during a family gathering. And honestly? I didn’t have a good answer ready.

    Because how do you explain to a child that their autistic cousin isn’t “getting away with” something, he’s protecting his nervous system from complete overwhelm?

    How do you help cousins or even siblings understand autism in a way that builds empathy instead of resentment?

    Both my son’s are autistic, but it makes me wonder. How do you make sure neurotypical siblings don’t feel invisible while you’re managing meltdowns, therapies, and endless accommodations?.

    These questions kept me up at night when Adrián was first diagnosed. And now, watching Guillermo (5) and Adrián (11) navigate their relationship as two autistic brothers with different needs, I’m still figuring it out.

    But I’ve learned some things along the way. And I want to share them with you, not as an expert, but as someone in the messy middle of this journey.

    Why This Conversation Matters So Much

    Here’s something I didn’t expect: how I talked about autism with Adrián’s cousins, friends, and eventually with Guillermo, shaped how Adrián felt about himself.

    When I used euphemisms or avoided the topic, Adrián heard: “There’s something wrong with you that we don’t talk about.”.

    When I spoke about autism matter-of-factly, with honesty and respect, he heard: “This is part of who you are, and it’s nothing to hide.”.

    The way we explain autism sets the tone for the entire family dynamic.

    What I Got Wrong at First

    Let me be honest about my early mistakes…

    Mistake #1: Using the “Superpower” Language

    “Autism is Adrián’s superpower!”……

    I said this with the best intentions. I wanted his cousins to see autism as positive.

    But here’s the problem: autism isn’t a superpower. It’s a neurotype.

    It comes with genuine strengths: Adrián’s incredible memory, his ability to focus intensely on topics he loves, his pattern recognition.

    But it also comes with genuine challenges: sensory overwhelm, social communication differences, anxiety about changes.

    Calling it a superpower set up unrealistic expectations. When Adrián had a meltdown or needed accommodations, his cousins were confused. “I thought autism was a superpower? Why does he need special help?”.

    Mistake #2: Only Talking About the “Special Needs”

    For a while, the only time I mentioned autism was when explaining why Adrián needed something different.

    “He needs headphones because of his autism.”…… “We’re leaving early because of his autism.”…… “He can’t handle that because of his autism.”……

    All my family heard this: Autism = limitations, problems, things that make family events harder.

    Mistake #3: Making It Too Clinical

    “Adrián’s brain is wired differently. His neurons fire in unique patterns that affect how he processes sensory input and social communication.”.

    I said this to a 6-year-old……

    His eyes glazed over. He had no idea what I was talking about.

    Kids need simple, honest, relatable explanations, not clinical jargon.

    Encouraging Conversations About Autism

    Encourage your kids to ask questions. It’s okay not to have all the answers. In fact, admitting “I’m not sure, let’s find out together” can be powerful. It shows your children that learning is a shared journey. Open dialogue helps them feel more comfortable expressing their thoughts and concerns.

    When his friends asked, “Why does Adrián flap his hands?” I used it as a teaching moment. I explained it’s one way he shows excitement or calms himself. “Just like when you sing your favorite song to feel happy,” I added. By relating it to their own experiences, it became less mysterious and more relatable to his friends.

    What Actually Works: The Conversations That Build Understanding

    After years of trial and error, here’s what I’ve learned about explaining autism to friends, cousins and even applied to siblings and other children in a way that actually helps.

    Start With “Different, Not Less”

    What I say now: “You know how everyone’s brain works a little differently? Some people are really good at math, some at art, some at sports. Adrián’s brain works differently too. It’s called autism. It means some things that are easy for you might be harder for him, and some things that are hard for you might be easier for him.”.

    Why this works: It normalizes differences without making autism sound like a tragedy OR a superpower. It’s just… a different way of being.

    Use Specific, Relatable Examples

    Instead of: “Adrián has sensory sensitivities.”.

    I say: “You know how when you eat a food you really hate, it makes you want to gag? For Adrián, certain sounds or lights feel that bad to him. So he uses headphones to make it more comfortable, just like you might close your eyes if a light is too bright.”.

    Why this works: Kids can relate to sensory experiences they don’t like. It helps them understand that Adrián isn’t being difficult, he’s managing something genuinely uncomfortable.

    Acknowledge the Hard Parts (For Everyone)

    What I say to my niece: “I know sometimes it’s frustrating when we have to leave places early because Adrián is overwhelmed. That’s hard for you, you want to stay and have fun. It’s hard for Adrián too, he wishes he could handle it but his body just can’t. And it’s hard for me because I want everyone to be happy. It’s okay that it’s hard.”.

    Why this works: Validating neurotypical feelings doesn’t mean you’re criticizing the autistic child. Both things can be true: This is hard AND we’re still going to do what’s needed.

    Celebrate the Unique Perspectives

    What I say: “Did you notice how Adrián remembered every single Roman emperor in order? His autism brain is really good at remembering details and patterns. That’s pretty cool, right?”.

    Or: “I love how Adrián tells you EXACTLY what he thinks. He doesn’t do fake compliments or say things just to be polite. When he says he likes your drawing, you know he really means it.”.

    Why this works: It helps see autism traits as neutral or positive, not just as problems to manage.

    The Book That Helped Us Have This Conversation

    When Adrián started asking questions about why he and Guillermo are “different kinds of different” (his words!), I realized I needed better tools.

    That’s why Luis and I wrote Autism: My Invisible Backpack.

    This book uses the metaphor of an invisible backpack that everyone carries, filled with emotions, experiences, and the weight of masking or managing challenges.

    Why it works for other kids like close friends, cousins or siblings:

    • It explains autism concepts (masking, sensory overload, literal thinking) in kid-friendly language

    • It shows that EVERYONE carries emotional weight, not just autistic people

    • It validates both the autistic experience AND the sibling experience

    • It opens conversations without feeling like a lecture.

    We’ve read it with both boys, and it’s helped Adri understand why Guille and himself sometimes needs breaks, why they get exhausted after school, why they do things differently.

    The Ongoing Conversations (Not Just One Talk)

    Here’s what I wish I’d known: you don’t have one conversation about autism and then you’re done.

    It’s an ongoing dialogue that evolves as children grow and their understanding deepens.

    Ages 3-5: Very Simple, Concrete

    “Adrián’s ears are more sensitive than yours. Loud sounds hurt him, so he wears special headphones.”.

    That’s it. Don’t overcomplicate.

    Ages 6-8: More Detail, Still Simple

    “Adrián has autism, which means his brain works differently. Some things are easier for him, like remembering facts. Some things are harder, like knowing when someone is joking. That’s why he sometimes takes things literally.”.

    Ages 9-12: Deeper Understanding

    “Autism means Adrián experiences the world differently. Sensory things like sounds and lights can be overwhelming. Social situations take more energy because he has to think about things that come naturally to you. That’s why he needs breaks and accommodations sometimes.”.

    Teens: Nuanced Conversations

    At this age, you can discuss masking, identity, the social model of disability, neurodiversity as part of human diversity.

    The conversations grow with the child. Start simple, add complexity as they can handle it.

    What About When close cousins or siblings Feel Jealous or Resentful?

    Let’s be real: sometimes neurotypical siblings DO feel jealous or resentful. My boys don’t have siblings but they do have very close cousins.

    “Adrián gets to stay home. I want to stay home too!”…… “Why does everything have to be about HIS needs?”…… “I never get this much attention.”……

    These feelings are valid. And they need to be acknowledged. Even sometimes Adrián even gets resentful for Guille there is a big age gap between them.

    What NOT to Say:

    ❌ “Don’t be selfish. Your brother has autism.”…… ❌ “You should be grateful you don’t have his challenges.”…… ❌ “Stop complaining.”……

    These responses shut down communication and breed resentment.

    What TO Say:

    ✓ “I hear you. It IS frustrating when we have to leave early. Your feelings matter too.”.

    ✓ “You’re right that Adrián gets a lot of my attention, especially when he’s struggling. That doesn’t mean I love you less. Let’s find some special time just for us.”.

    ✓ “Sometimes it feels unfair that Adrián gets different rules. The truth is, everyone in our family gets what they need, and those needs are different. You need different things than he does, and that’s okay too.”.

    Validation doesn’t mean you change the accommodations. It just means you acknowledge that this is hard for everyone.

    Building Empathy Without Parentifying Siblings

    Here’s a trap I almost fell into: making my neurotypical nephew feel responsible for understanding, helping, and accommodating Adrián.

    “You need to be patient with your cousin.”…… “Can you help Adrián with this?”…… “You’re such a good helper!”……

    While building empathy is important, siblings shouldn’t become mini-therapists or mini-parents.

    The Balance:

    YES to: “It’s kind when you’re patient with Adrián.”. NO to: “You HAVE to be patient with Adrián. He can’t help it.”.

    YES to: “Thanks for thinking of Adrián’s needs.”. NO to: “You’re responsible for making sure Adrián is okay.”.

    Empathy is a gift, not an obligation. Siblings can choose to be understanding, but it shouldn’t be forced or expected at the expense of their own needs.

    Creating Family Rituals That Include Everyone

    One thing that’s really helped our family: creating traditions and rituals that honor both boys’ needs.

    Our “Everyone Picks” System

    Every Friday, each family member picks one thing we do together. It rotates.

    • Adrián might pick: Watch a documentary about trains

    • Guille might pick: Dance party in the living room

    • I might pick: Family walk

    • Luis might pick: Game night.

    Everyone’s interests are valued equally. No one’s needs dominate.

    Celebrating Different Wins

    When Adrián reaches a milestone (like getting through a school assembly without leaving), we celebrate.

    But we ALSO celebrate when Guillermo reaches HIS milestones (like trying a new food).

    Every child deserves to have their growth acknowledged.

    With love and understanding,
    Dalisse (& Luis)
    Loving Pieces Books

    💙 How have you explained autism to siblings in your family? What’s worked? What’s been hard? Share with our community—we’re all learning together. Find us on Instagram @lovingpiecesbooks or explore more resources at lovingpiecesbooks.com.

  • Empowering Our Autistic Kids: Nurturing Self-Advocacy from a Young Age

    • by

    Empowering Our Autistic Kids: Nurturing Self-Advocacy from a Young Age

    Self-advocacy isn’t something kids just magically know how to do—it’s a skill we have to gently teach and practice, especially with autistic children. I’ve stumbled through this myself, watching my boys find their voices in a world that often misunderstands them. If you’re looking for parenting tips and practical ways to support your child’s confidence and self-expression, you’re in the right place. Let’s walk this path together, learning how to nurture self-advocacy from the very start.

    Cultivating Self-Advocacy Skills

    Helping our children find their voices is a rewarding journey. It’s about more than just teaching them to speak up; it’s about building confidence and understanding their unique perspectives.

    Starting Conversations Early

    The best time to start teaching self-advocacy is when your child is young. Begin by encouraging them to express their thoughts and preferences. You might start simply by asking them what they want for a snack or which activity they’d prefer to do. These small choices empower them.

    Try to create opportunities for your child to make decisions. It could be as simple as choosing their clothes or deciding which book to read before bed. By doing so, you’re showing them that their opinions matter. It’s a way of saying, “Your voice counts.” When children feel heard, they are more likely to speak up in other areas of their lives.

    Building Confidence Through Stories

    Stories can play a powerful role in helping autistic children build self-confidence. When they see characters who share similar experiences, it can be incredibly validating. Imagine reading a story together where the main character successfully navigates a situation your child faces. This can be a great conversation starter.

    You can ask questions like, “How do you think they felt?” or “What would you do in their place?” These discussions can help your child reflect on their own experiences and develop a deeper understanding of themselves. Plus, it opens the door for them to share their thoughts and feelings, reinforcing their ability to advocate for themselves.

    Creating Inclusive Environments

    Building a world where our children feel included starts with their immediate surroundings. Schools, homes, and communities should all reflect acceptance and understanding.

    Empowering Through Education

    Education is a key factor in creating a supportive environment for autistic children. It starts with helping teachers and classmates understand autism. Simple explanations about what it means to be autistic can go a long way. You might work with teachers to present a short lesson or share a book with the class that explains autism in an accessible way.

    When children understand the diversity in their classroom, they learn empathy. They’re more likely to include and support each other. For parents, it’s important to engage with educators to ensure that your child’s needs are met. Ask questions, share insights about your child, and collaborate to create a nurturing educational environment.

    Encouraging Expression and Choice

    Encouraging kids to express themselves and make choices helps them feel more in control. At home, create spaces where your child can relax and be themselves. This might mean having a quiet corner with sensory toys or a cozy reading nook.

    Invite your child to participate in creating these spaces. Ask them what makes them feel comfortable and safe. By giving them a say in their environment, you’re reinforcing their ability to make choices and express their needs. This practice at home can boost their confidence in other settings.

    Fostering a Supportive Community

    Communities thrive when everyone feels valued and supported. Let’s focus on building connections that uplift our autistic children.

    Sharing Parenting Tips and Insights

    Connecting with other parents can provide valuable insights. Share your experiences and hear theirs. Maybe you’ve developed a morning routine that works wonders, or perhaps another parent has a strategy for handling transitions that you haven’t tried yet.

    Consider joining local support groups or online communities. These spaces can be invaluable for sharing resources and encouragement. They remind us that we’re not alone in this journey.

    Celebrating Neurodiversity Together

    Embracing neurodiversity is about celebrating every child’s unique abilities. Encourage your community to host events that highlight these strengths. Whether it’s an art show, a talent night, or a simple gathering, these events can foster understanding and appreciation.

    When we create spaces that celebrate differences, we’re teaching our children that they belong and are valued. It’s these positive experiences that build a child’s self-esteem and reinforce their ability to advocate for themselves.

    🌟

    In nurturing self-advocacy, we’re not just teaching our children to speak up; we’re giving them the tools to thrive in a world that doesn’t always understand them. Together, we can create a supportive community where every child feels seen and heard.

    Check out our books and FREE Resources

  • Empowering Voices: Encouraging Self-Advocacy in Autistic Children

    • by

    Empowering Voices: Encouraging Self-Advocacy in Autistic Children

    Most people think self-advocacy in autistic children just happens naturally. I used to believe that too—until I saw my own sons struggle to express their needs and set boundaries. Nurturing autistic self-advocacy takes patience, understanding, and the right tools. In this post, I’ll share what’s helped our family build confidence and voice in our boys, so your child can feel truly seen and heard.

    Nurturing Autistic Self-Advocacy Skills

    Helping your child find their voice can be the most rewarding journey. Confidence grows when communication channels are clear and supportive.

    Building Confidence Through Communication

    Imagine your child asking for what they need without hesitation. This dream is possible. Start with small steps. Encourage them to express preferences—like choosing between two snacks. These moments build confidence. When my son Adrián first voiced his choice, it was magical. It reminded me that our kids have strong opinions; they just need encouragement to share them.

    Create opportunities for dialogue. Ask open-ended questions like, “What do you think about this?” It invites your child to explore their thoughts. Use visual aids or storyboards if words are hard. These tools can help them express complex feelings more easily.

    Creating Safe Spaces for Expression

    A safe environment is crucial. Make sure your home feels like a sanctuary where your child can speak freely. I remember setting up a cozy corner with soft lights and familiar objects for Adrián. It became his retreat—a place where he felt secure.

    Encourage them to use this space whenever needed. It fosters a sense of ownership over their environment and emotions. Over time, Adrián’s corner became a place of creativity and reflection. Your child can have this too—a space to be themselves, free from judgment.

    Practical Strategies for Empowering Autistic Children

    Empowering your child starts with understanding their world. Help them navigate it by setting and respecting boundaries.

    Encouraging Boundaries and Self-Awareness

    Teaching boundaries is essential. Start by modeling them yourself. When you say, “I need a moment,” you’re showing self-care. This teaches your child it’s okay to do the same. Adrián learned to say, “I need a break,” when overwhelmed. It was a game-changer for us.

    Help your child recognize their body’s signals. Does their heart race in noisy places? Do bright lights cause discomfort? Discuss these sensations openly. This awareness allows them to set effective boundaries, creating a roadmap for self-advocacy.

    Using SEL Resources in Everyday Life

    Social Emotional Learning (SEL) tools are invaluable. They teach essential skills like empathy and self-regulation. Incorporate simple SEL activities into daily routines. For instance, use role-playing to explore different scenarios. It can be as fun as pretending to order at a restaurant.

    Books and stories are also effective. They offer relatable scenarios that foster understanding. In our family, reading together has opened up conversations about emotions and challenges. It’s a bonding experience that also empowers.

    Cultivating an Inclusive Education Environment

    The school setting should echo the supportive environment you cultivate at home. It’s essential for fostering a sense of belonging.

    Supporting Neurodiversity in the Classroom

    Talk to your child’s teachers about their unique needs. Most educators want to help but need guidance. Share what works at home. Maybe it’s a particular seating arrangement or the use of headphones during tests.

    Encourage classrooms to decorate with diverse materials that celebrate neurodiversity. Visual aids and sensory-friendly tools should be standard. These adjustments make a world of difference, helping your child feel understood and valued.

    Collaborative Efforts with Parents and Educators

    Building a network of support is key. Regularly communicate with teachers and staff. They are your partners in this journey. Share successes and challenges openly. This collaboration creates a unified front that benefits your child.

    Join or form parent support groups. We did, and it’s been a lifeline. Sharing resources and strategies with other parents has been invaluable. It creates a community where everyone learns and grows together, ensuring no one feels isolated.

    🙌📚

    By implementing these strategies, you’ll help your child develop a strong voice and a sense of self. Remember, progress may be slow, but each step is significant. Your child’s journey to self-advocacy is not just about them—it’s about creating a world that listens and values every unique voice.

    Check out our books and FREE Resources

  • Creating Mask-Free Zones: A Loving Approach to Authenticity at Home and School

    • by

    The Day They Told Me Adrián Was “Acting Normal” at School

    A good friend of Adrián told me at pick-up “Adrián, Is SO tired, but he was acting normal all day.”

    “What do you mean, ‘acting normal’?” I asked..

    “You know… making eye contact. Not stimming. Sitting still. Acting like other kids.”

    My heart broke. Because I realized: my son was masking. And he was exhausted from it.

    That conversation changed everything for our family. It’s why Luis and I became obsessed with creating mask-free zones, spaces where Adrián (and now Guille) never have to pretend to be anything other than exactly who they are.

    If your autistic child is exhausted, withdrawn, or having meltdowns after seemingly “good” days, masking might be why. And creating mask-free zones might be the answer.

    What IS Masking? (And Why It’s So Exhausting)

    Masking is when autistic people hide or suppress their natural autistic traits to fit in with neurotypical expectations.

    It looks like:

    • Forcing eye contact when it’s uncomfortable

    • Suppressing stims (no hand-flapping, no rocking, no vocal sounds)

    • Scripting conversations instead of speaking naturally

    • Pretending to understand social cues they actually don’t get

    • Hiding sensory sensitivities

    • Mirroring others’ body language and expressions

    • Acting interested in things they find boring.

    And here’s the cost: It’s exhausting!

    Imagine spending every moment of your day monitoring your body language, your facial expressions, your tone of voice. Imagine suppressing your natural movements and responses. Imagine translating every social interaction like you’re speaking a foreign language.

    That’s what masking feels like. And that’s what Adrián was doing all day, every day, at school.

    Why Kids Mask

    Adrián didn’t consciously decide one day to start masking. It happened gradually.

    He learned that:

    • Adults praised him when he made eye contact

    • Kids stopped staring when he stopped stimming

    • Adults thought he was “doing better” when he sat still

    • People were nicer to him when he “acted normal”

    So he learned to hide who he really was to make others more comfortable.

    And the heartbreaking part? He thought this was what he was supposed to do…

    The Signs Your Child Might Be Masking

    I didn’t recognize Adrián’s masking for years because at school, he seemed “fine.” His teachers said he was doing well. He wasn’t having meltdowns there…

    But at home? Different story.

    The After-School Collapse

    Within 20 minutes of getting home, specially in the early years Adrián would have a meltdown. Over tiny things, wrong snack, homework, his brother existing……

    I thought, “Why does he save all this for me?”

    Now I know: He was holding it together all day, and home was the only place safe enough to fall apart.

    The Weekend Shutdown

    Fridays through Sundays, Adrián would barely speak. He’d retreat to his room, avoid family activities, resist any plans.

    I worried he was depressed…

    But he was recovering from a week of masking. He needed that quiet, that solitude, that lack of demands.

    The Loss of Authentic Interests

    Adrián stopped talking about trains at school, his biggest passion, because other kids didn’t share that interest……

    He’d come home and talk about popular shows he didn’t even like, repeating things he’d heard other kids say……

    He was losing himself trying to fit in.……

    Physical Symptoms

    Headaches. Stomach aches. Trouble sleeping. These all increased during the school year and eased during breaks.

    Masking isn’t just emotionally exhausting, it’s physically draining.

    Creating Mask-Free Zones at Home

    Once I understood what was happening, Luis and I committed to making our home a place where masking was never necessary.

    Rule #1: Stimming Is Always Welcome

    Before: “Adrián, hands still.” “Stop making that sound.” “Sit properly.”……

    Now: Our home is a stim-friendly zone. Hand-flapping? Great. Vocal sounds? Go for it. Pacing while thinking? Perfect.

    We don’t just allow stimming, we celebrate it as part of who he is.

    Guille watches his brother stim freely and is learning that his own stims (spinning, jumping, echolalia) are perfectly okay too.

    Rule #2: No Forced Eye Contact

    In our home, you never have to look at someone to show you’re listening. ( I do this all the time as an Autistic Adult)

    Luis and I have learned to trust that Adrián is paying attention even when he’s looking away, building LEGO, or lying on the floor.

    Sometimes his best conversations happen while he’s doing something else with his hands.

    Rule #3: Honest Answers Are Valued

    “How was your day?”……

    Before, Adrián would say: “Fine.”…

    Now, he might say: “Loud and overwhelming. I’m glad to be home.”

    We don’t pressure him to be positive or polite. We want honesty. Even if that honesty is “I don’t want to talk about it right now.”

    Rule #4: Special Interests Are Treasured

    Adrián can talk about Roman history for an hour, and we listen. Not politely waiting for him to finish, but actually interested because his passion is beautiful.

    When he brings home a new fact about steam engines, we don’t redirect. We engage.

    His special interests aren’t annoying quirks to manage. They’re windows into what makes him amazing.

    Rule #5: “No” Is a Complete Sentence

    Family gathering? “Can I stay home?”…… Trying a new food? “No thanks.”…… Hug from a relative? “I’d rather not.”……

    In our home, Adrián doesn’t have to justify his boundaries. We trust that he knows what he needs.

    The Physical Space Matters Too

    Adrián’s room is his ultimate mask-free zone:

    • Dim lighting (he controls it)

    • His collections displayed proudly (trains, historical figures, maps)

    • Comfortable clothing only (tags cut out, soft fabrics)

    • Sensory tools within reach

    • No expectations for organization (his “mess” makes sense to him).

    This is HIS space. We don’t impose our neurotypical preferences on it.

    What About School? (Can We Create Mask-Free Zones There?)

    Here’s the harder truth: school is where masking happens most intensely.

    But Luis and I have worked with Adrián’s teachers to create moments of mask-free time, even in that environment, they are experienced and have given us peace of mind and working along with the therapists and us parents has been a life-saver:

    What We’ve Agreed together (Teacher-Therapist-Parents):

    ✓ Fidget tools during class – Adrián can use a fidget while listening. It helps him focus, not distract him……

    ✓ Movement breaks – Built into the schedule, not earned through “good behavior”……

    ✓ Alternative seating – Specially younger, Adrián uses a wobble cushion instead of sitting rigidly still……

    ✓ Reduced eye contact expectations – His teacher understands he’s listening even when not looking……

    ✓ A quiet lunch option – Instead of the overwhelming cafeteria, he can eat in the library with a small group……

    ✓ Special interest integration – When possible, assignments connect to his interests (he did a history project on trains and thrived)……

    ✓ Acceptance of stims – As long as he’s not disrupting others’ learning, his stims are welcomed……

    The Conversation With Teachers

    Luckily we never tiptoe around asking for accommodations, worried about being “that parent.”……

    We believe a honest and truthful conversation with teachers is the best way to go.

    “Adrián masks heavily at school to meet neurotypical expectations. It’s exhausting for him and leads to meltdowns at home. Can we work together to reduce the need for masking during the school day?”

    You might find that some teachers get it immediately. Others need ideas and tips. But starting the conversation has made a huge difference……

    For Educators: How to Create Mask-Free Moments

    If you’re a teacher reading this, here’s what would help autistic students in your classroom:……

    Start With Awareness

    Recognize that the “well-behaved” autistic student who never causes problems might be masking intensely, and paying a huge price for it.

    Build In Regulation Time

    Don’t make breaks something kids have to earn. Build them into the day for everyone.

    Adrián’s best teacher had a “sensory break” built into the schedule every 90 minutes. ALL students benefited, not just the autistic ones.

    Challenge Your Own Expectations

    Does a student really need to make eye contact to show respect? Do they really need to sit completely still to be learning?

    Often, we’re requiring masking without realizing it.

    Create Quiet Options

    Not every child thrives in group activities or loud environments. Having a quiet alternative isn’t “special treatment”, it’s meeting different needs.

    Celebrate Neurodiversity

    When you openly value different ways of thinking, moving, and being in your classroom, you send the message that masking isn’t required.

    Display neurodiversity-affirming posters. Read books with autistic characters. Talk about different learning styles as equally valid.

    This benefits all students, not just autistic ones.

    The Cost of Masking (Why This Matters So Much)

    I want to be clear about something: masking isn’t harmless.Research shows that prolonged masking is linked to:

    • Burnout and exhaustion

    • Anxiety and depression

    • Loss of identity and sense of self

    • Delayed recognition of one’s own needs

    • Increased risk of suicide in autistic adults..

    When Adrián tells me he is “tired of acting normal,” that was a warning sign……

    Creating mask-free zones isn’t just about comfort. It’s about mental health. It’s about allowing our kids to know and be themselves.

    What You Can Do Today: 5 Steps to Honor Your Child’s True Self

    These are the shifts I wish I had made sooner. They’re not about fixing your child, but about changing the environment to let their true self shine.

    1. Recognize the Masking
    Notice the pattern of “good days at school / meltdowns at home.” It’s not defiance, it’s often the exhausting cost of masking all day. That meltdown is the backpack of anxiety finally being unpacked.

    2. Declare Home a Mask-Free Zone
    Tell them, explicitly and often: “You never have to hide who you are in this house.” This verbal permission can be a profound relief.

    3. Model Your Own Authenticity
    After my own diagnosis, I stopped masking my own autistic traits at home. When he saw me stim, or need quiet, or be blunt about my feelings, it gave him silent, powerful permission to do the same.

    4. Advocate Boldly, Not Apologetically
    I was too worried about being a “difficult parent.” I wish I’d pushed harder, sooner, for the supports he needed. You are not being difficult; you are being necessary.

    5. Celebrate, Don’t Just Tolerate
    Move beyond allowing his traits to actively celebrating them. That intense focus? It’s passion. That need for routine? It’s brilliant foresight. Name the strength behind the behavior.

    Resources That Have Helped Us

    If you’re realizing your child has been masking and you want to create safer spaces for them, here’s what has genuinely helped our family:

    📚 Autism: My Invisible Backpack – This book explores masking from Adrián’s perspective and includes strategies for creating mask-free zones.

    And we’ve created FREE downloadable resources including:

    • Creating Mask-Free Zones guide

    • Accommodations request template for schools

    • Recognizing masking checklist

    • Building authentic confidence activities……

    Your child shouldn’t have to earn the right to be themselves. They should know it’s a given, at least in the spaces you control.

    With love and authenticity,
    Dalisse (& Luis)
    Loving Pieces Books

    💙 Does your child mask? How do you create safe spaces for authenticity? Share with our community, we’re all learning together. Find us on Instagram @lovingpiecesbooks or explore more resources at lovingpiecesbooks.com.

  • Unpacking Your Child’s Invisible Backpack: A Journey Toward Emotional Understanding

    • by

    When Your Child’s Invisible Backpack Gets Too Heavy to Carry

    Five o’clock pickup. Every day.

    I watch Adrián walk out of school, and I can see it, the weight he’s been carrying all day finally starting to show.

    His shoulders are tense. His face is tight. His usual animated energy? Gone!

    By the time we get to the car, he’s barely speaking. And by the time we get home? Full meltdown!

    For years, I thought I was doing something wrong. Why does he hold it together at school but fall apart at home? Why is he so exhausted after a “normal” day?

    We came up with a concept that changed everything: the invisible backpack…

    Every autistic child carries one. And most of us… parents, teachers, even the kids themselves, don’t realize how heavy it gets.

    What IS the Invisible Backpack?

    Imagine starting your day with an empty backpack.

    But every sensory input… every fluorescent light buzz, every unexpected loud noise, every texture that feels wrong, every social interaction that requires masking+adds a stone to that backpack.

    By lunchtime, it’s getting heavy!

    By afternoon, it’s almost unbearable.

    By the time your child gets home, their safe place, that backpack is so full, so heavy, that it all comes tumbling out…

    That’s what I was seeing with Adrián.

    He wasn’t “fine all day and then acting out at home.” He was holding it together where he had to, then finally releasing the weight where he felt safe enough to let go.

    Understanding this changed how I saw those after-school meltdowns. They weren’t behavior problems. They were evidence of how hard he’d been working all day just to keep it together.

    The Signs I Wish I’d Recognized Sooner

    Looking back, Adrián was showing me his backpack was getting heavy. I just didn’t know what I was looking at.

    The Quiet Withdrawal

    SOme days when Adrián comes home from school, he used to immediately go to his room. No hello. No “how was your day?” Just… retreat……

    I thought he was being rude or antisocial. But he was seeking the quiet, the solitude, the sensory reduction he desperately needed after hours of holding it together.

    Now I understand: That withdrawal isn’t rejection. It’s self-preservation.

    The Delayed Meltdowns

    Adrián would have a great day at school, his teacher would tell me so. Then he’d come home and have a massive meltdown over something tiny, or something that happened ages ago.

    I couldn’t understand the disconnect. If school was good, why the meltdown?

    Because the backpack doesn’t empty instantly. Just because he made it through the day doesn’t mean the emotional and sensory load disappears. It needs to be unpacked, and sometimes that unpacking is messy.

    The Exhaustion

    On weekends, Adrián would sleep late, move slowly, resist any plans or outings.

    I worried he was depressed or lazy. But he was exhausted. Carrying that invisible backpack all week is genuinely, physically draining…

    Now I know: He needs that recovery time. It’s not optional…

    For Guillermo (My 5-Year-Old)

    Guille’s backpack signs look different:

    • Increased stimming – More hand-flapping, more spinning, more vocal sounds

    • Regression in skills – Losing words he had earlier, needing more help with things he usually does independently

    • Physical symptoms – Headaches, tummy aches, difficulty sleeping

    • Clinginess – Not wanting to separate from me or Luis, even for short periods…

    The backpack fills differently for every child. But it always fills.……

    What Goes IN the Invisible Backpack?

    Let me walk you through a typical school day for a child, and show you how the backpack could get filled up:

    7:00 AM – Morning routine
    Stones added: Rushing, loud noises from breakfast, bright bathroom lights, uncomfortable school clothes with tags. Nervousness of getting late to school because unexpected traffic or something else.

    8:30 AM – Arrival at school
    Stones added: Crowded hallway, multiple conversations at once, fluorescent lights, unexpected schedule change announced.

    9:00 AM – Classroom
    Stones added: Sitting still for long periods, maintaining “appropriate” body language, suppressing stims, making eye contact when called on…

    12:00 PM – Lunch
    Stones added: Loud cafeteria, overwhelming smells, navigating social interactions, someone sitting too close, unexpected fire drill…

    3:00 PM – End of day
    Stones added: Transition to dismissal, crowded hallway again, loud buses, holding everything in “just a little longer”…

    By the time he gets home? That backpack is FULL!!!!!

    And as parents we tend to add MORE by immediately asking questions, making demands, expecting him to transition right into homework or chores…

    No wonder this can escalate to a meltdown……This is why it´s so important to unpack with Care

    How We Help Adrián and Guillermo Unpack their Backpacks

    Once I understood what was heavy, Luis and I completely changed our after-school routine.

    Step 1: Quiet Arrival

    Before: “Hi! How was your day? What did you learn? Did you have fun? What’s for snack? When’s homework?”……

    Now: “Hi, love. We missed you all day.” Then… silence. Space. No demands……

    Car ride home in silence. Adrián goes straight to his room for 20-30 minutes. No questions asked… And Guillermo audits the house to make sure we did not change his toys.

    Step 2: Sensory Reset

    In his room, Adrián has:

    • Dim lighting (a Salt Lamp does the trick for him and Guillermo)

    • His favorite comfort items (currently TV with his favorite Youtube train channels)

    • Permission to stim freely, no one’s watching, no one’s judging…

    This isn’t avoidance. This is regulation...

    Step 3: Gradual Reentry

    After his alone time, Adrián emerges when he’s ready. Sometimes it’s 20 minutes. Sometimes it’s an hour. We follow his lead…

    When he does come out, we offer:

    • A preferred snack (he chooses)

    • Quiet activity options (Playing with his books, or train sets or just any game at the playroom)

    • Casual presence (we’re available if he wants to talk, but we don’t push), he usually leads the talks specially with his ecolalias and infodumping.

    Step 4: Delayed Conversations

    We used to have “the talk” about his day immediately. Now? We wait…

    After dinner, when he’s regulated and comfortable, we might ask gentle questions:

    • “Want to tell me about your day?”

    • “Anything you’re proud of from today?”

    • “Anything that was hard?”……

    He can say “not right now” and that’s okay. Sometimes we don’t process the day until the next morning…

    For Guillermo

    At 5, Guille can’t articulate his backpack yet. So we read his body:

    • If he’s clingy: Extra physical closeness, weighted lap pad while he watches his show

    • If he’s overstimulated: Dim lights, quiet environment, maybe a bath with gentle music

    • If he’s about to have a meltdown: Safe space to let it out, minimal talking, just presence…

    We’re teaching him language for his feelings, but right now, our job is mainly to recognize the signs and provide the support…

    Building Emotional Vocabulary (Without Adding Pressure)

    Here’s something that helped Adrián understand his own backpack: giving him language for what he was experiencing…

    We use a “backpack check-in” now. It’s simple:

    “How full is your backpack right now?”

    • Empty

    • A little full

    • Medium full

    • Pretty full

    • Overflowing…

    Adrián can point to a visual chart or just say the words. This gives him a way to communicate his internal state without having to explain everything.

    We also practice naming emotions when he’s calm:

    • “Remember yesterday when you felt overwhelmed? Your backpack was pretty full.”

    • “Today you seemed more relaxed. Your backpack wasn’t as heavy.”

    This isn’t therapy homework. It’s just giving him tools to understand himself.

    What About School? (Creating Mask-Free Zones There Too)

    I’ve had honest conversations with Adrián’s teachers about the invisible backpack… our school has a lot of experience with special needs students so this has giving us more peace of mind.

    Some things that have helped Adrián and Guillermo that they practice at school:

    ✓ Sensory breaks built into the day – Not as a reward or punishment, just regular breaks where Adrián and Guillermo can regulate

    ✓ A quiet space option – A corner of the library or resource room where he can go if his backpack is getting too full. They have one in the classroom, all the kids use it.

    ✓ Reduced expectations for eye contact and “looking interested” – Letting him stim, letting him look away while listening, trusting that he’s still engaged

    ✓ Heads up about changes – Advance notice when possible about schedule changes, substitute teachers, fire drills

    ✓ Understanding after-school needs – His teacher doesn’t pile on homework or expect lengthy parent communications at pickup. She gets it…

    Not all teachers understand this immediately. But starting the conversation, explaining the invisible backpack metaphor, has opened doors to many parents……

    The Guilt I Had to Let Go Of

    For years, I felt guilty about those after-school meltdowns.

    What am I doing wrong? Why can’t I make coming home easier? Other kids don’t do this..

    But here’s what I finally understood: Adrián having a meltdown at home isn’t a sign of failure. It’s a sign of trust.

    He feels safe enough with us to let down his mask, to release the weight, to be vulnerable… same with Guillermo.

    That’s not something to fix. That’s something to honor.

    My job isn’t to prevent them from ever having a full backpack. My job is to help my sons unpack their own backpacks safely.

    For Guille’s Future

    At 5, Guille is just beginning to navigate the world with his invisible backpack.

    We’re starting early with:

    • Creating mask-free zones at home where he never has to hide who he is

    • Teaching him words for his feelings as they emerge

    • Modeling unpacking our own “backpacks” (yes, I have one too as an autistic adult)

    • Building in regulation time as part of the routine, not as a response to crisis……

    The goal isn’t to eliminate the backpack. The world will always add stones to it. That’s reality.

    The goal is teaching him to recognize when it’s getting heavy and giving him tools to unpack it before it overflows.

    Resources That Have Helped Us

    If you’re realizing your child has been carrying an invisible backpack and you want to support them better, here’s what has genuinely helped our family:

    📚 Autism: My Invisible Backpack – This is the book Luis and I wrote specifically about this concept. It explains masking, emotional overload, hyper-empathy, and the invisible load autistic kids carry, told through Adrián and Guillermo’s perspective……

    📚 Autism: Calming the Chaos – Helps kids and parents understand what happens when the backpack gets too full and overflows into a meltdown……

    And we’ve created FREE downloadable resources including:

    • Invisible Backpack visual chart

    • Emotion identification cards

    • After-school routine templates

    • Mask-free zone planning guide…

    That 5:00 PM pickup doesn’t scare me anymore……

    I no longer worry when Adrián walks out of school looking exhausted. I no longer panic when he immediately retreats to his room. I no longer feel guilty about the evening meltdowns.

    Because I understand what his invisible backpack is carrying. And I know how to help him unpack it.

    Your child is carrying weight you can’t see. But once you understand it’s there, everything changes.

    You stop seeing behavior problems and start seeing a child who needs support.

    You stop feeling like you’re failing and start feeling like you’re finally seeing clearly.

    And your child? They feel less alone carrying that weight.

    With understanding and solidarity,
    Dalisse (& Luis)
    Loving Pieces Books

    💙 Does your child carry an invisible backpack? What signs do you see? Share with our community, we’re all learning together. Find us on Instagram @lovingpiecesbooks or explore more resources at lovingpiecesbooks.com.

  • The Story Behind ‘Calming the Chaos’: A Personal Journey

    • by

    The Story Behind ‘Autism: Calming the Chaos’: A Personal Journey

    The first time Adrián had a public meltdown, I felt like the entire world was watching me fail as a mother.

    We were at a park, should have been joyful, playful. Instead, I was sitting on a bench with my 3-year-old son, both of us crying, while nobody could help us.

    I didn’t understand what was happening. I didn’t know how to help him. And I felt so utterly, completely alone.

    That park moment? That’s where “Autism: Calming the Chaos” was born……

    Not in that exact moment, obviously. But that feeling, of being lost in the chaos, desperate for understanding, needing someone to tell me “this is what’s happening and here’s how to help”, that’s what drove Luis and me to write this book……

    This week, as a thank you to our community, we’re offering the Kindle eBook version completely FREE (December 2-6). Because if even one family can skip that park moment I had, if even one parent can understand their child’s meltdowns sooner than I did… it’s worth it!

    Get your FREE copy here (available Dec 2-6 only)

    A Mother’s Love and Honest Struggles

    Let me be real with you about something: I love my boys more than anything in this world……

    Adrián, who’s 11 now, with his intense passion for history and trains. Guillermo, my 5-year-old, who sees the world through the most beautifully unique lens……

    But loving them fiercely doesn’t mean parenting them has been easy……

    There have been days when I’ve sat in my car after dropping Adrián at school, just crying. Days when the meltdowns felt relentless and I questioned everything I was doing. Days when I felt like I was failing them……

    The hardest part? Watching them struggle and not knowing how to help……

    Seeing Adrián cover his ears in pain at sounds I barely noticed……

    Watching Guillermo become completely overwhelmed by changes to his routine that seemed minor to me……

    Holding them through meltdowns, feeling helpless, wondering what I was doing wrong……

    That’s the love that propelled me to write this book……

    Not a sanitized, Instagram-perfect version of autism parenting. But the real, messy, beautiful, challenging truth of it……

    Because I wanted other parents to know: you’re not alone in those hard moments. You’re not failing. Your child isn’t broken. And there ARE things that can help……

    The Daily Moments That Became Our Guide

    “Autism: Calming the Chaos” isn’t based on research studies or clinical observations (though those informed it)……

    It’s based on our actual life……

    Like the time Adrián had a meltdown at the grocery store because the fluorescent lights were buzzing at a frequency I couldn’t even hear. I thought he was “overreacting.” But he was in genuine pain……

    Like the morning Guillermo melted down for 45 minutes because we took a different route to preschool. Not because he was being “difficult,” but because the unexpected change felt destabilizing to his entire nervous system……

    Like the birthday party where Adrián (in his own party) retreated to a quiet room for 30 minutes, and instead of forcing him to “participate,” we let him regulate, and he came back ready to engage on his terms……

    These real moments taught us what actually works……

    Not theories. Not “shoulds.” But practical strategies born from trial, error, tears, and eventual understanding……

    Every strategy in this book? We’ve lived it……

    The calm-down corner we describe? That’s in our house. Adrián and Guillermo uses it regularly……

    The sensory regulation tools? Those are in Guillermo’s backpack right now……

    The scripts for talking to kids about meltdowns? Those are the exact words we use with our boys……

    This book is our family’s lived experience, offered to yours 💙

    Understanding What’s Actually Happening

    Here’s what I wish someone had told me years ago: meltdowns are not behavior problems. They’re neurological responses to overwhelm……

    When Adrián has a meltdown, it’s not because he’s trying to manipulate me or get his way. It’s because his nervous system has hit overload and the thinking, rational part of his brain has gone offline……

    Understanding that changed everything for us……

    Recognizing the Signs (Before It’s Too Late)

    Over the years, Luis and I have learned to read the early warning signs:……

    For Adrián:

    • He gets quieter than usual

    • His stimming increases (hand-flapping, pacing)

    • He starts avoiding eye contact even more than usual

    • His responses become shorter, more clipped

    For Guillermo:

    • He starts covering his ears

    • His speech becomes more echolalic (repeating phrases)

    • He seeks out tight spaces

    • His movements become more frantic

    When we catch these signs early, we can often prevent a full meltdown by:

    • Moving to a quieter space

    • Reducing demands

    • Offering sensory tools

    • Just… giving them space and time……

    This is what we teach in the book—not just how to manage meltdowns once they happen, but how to recognize and respond to the signs before things escalate……

    The Self-Management Strategies We Actually Use

    Here’s the truth: you can’t stop all meltdowns. Sometimes the world is just too much, and that’s okay……

    But you CAN give your child tools to manage their nervous system……

    For Adrián, we’ve taught him:

    • To recognize when he’s getting overwhelmed (using a “feelings thermometer”)

    • To ask for breaks before he hits his limit

    • To use his calm-down corner when he needs it

    • To identify which sensory tools help him most (noise-canceling headphones, weighted blanket, dim lighting)

    For Guillermo, we’re working on:

    • Visual emotion cards to help him identify feelings

    • Simple phrases like “too loud” or “need quiet”

    • Using his comfort items when overwhelmed

    • Understanding that big feelings are okay

    The book walks through these strategies step-by-step, from Adrián’s perspective as a 10-year-old autistic boy, so kids can understand what’s happening in THEIR bodies and what they can do about it……

    Why Adrián’s Voice Matters

    One of the things that makes “Autism: Calming the Chaos” different is that it’s told from Adrián’s perspective……

    With the help of my perspective as a autistic parent myself observing from the outside……

    But mainly from a 10-year-old autistic boy explaining what a meltdown actually FEELS like from the inside……

    Why does this matter?

    Because when autistic kids read this book, they see themselves. They understand “Oh, that’s what’s happening to ME. I’m not weird. I’m not bad. This is just how my brain works.”……

    And when parents, teachers, siblings, and grandparents read it, they finally understand: “Oh, THIS is what my child/student/grandchild is experiencing. No wonder they respond this way.”……

    Adrián helped us write this book. His insights, his experiences, his voice (even for the time when he was non-verbal), it’s all woven throughout……

    That’s what makes it authentic……

    Building Understanding Through Our Story

    When we decided to write this book, we made a choice: we would be honest. Even about the messy, hard parts……

    We don’t sugarcoat meltdowns in this book. We don’t pretend they’re easy to navigate. We don’t offer miracle cures……

    What we DO offer: ✨ Real understanding of what meltdowns are (and aren’t) ✨ Practical strategies that have actually worked for our family ✨ Compassionate guidance for supporting your child before, during, and after overwhelm ✨ A perspective that treats autistic traits with respect, not as problems to fix ✨ Hope, because understanding changes everything……

    For the Kids Reading This Book

    When autistic children read “Autism: Calming the Chaos,” they learn:

    • What’s happening in their body during a meltdown

    • That meltdowns don’t make them “bad”

    • Practical strategies they can use themselves

    • That they’re not alone, other kids experience this too

    • That their feelings and experiences are valid……

    Several parents have told us their kids return to this book again and again, especially after a hard day. It validates them. It helps them understand themselves……

    For the Adults Reading This Book

    When parents, teachers, and caregivers read it, they learn:

    • The difference between meltdowns and tantrums (game-changer!)

    • Common triggers and how to identify YOUR child’s specific triggers

    • What to do (and what NOT to do) during a meltdown

    • How to support recovery after overwhelm

    • How to build prevention strategies into daily routines……

    Plus, there’s an entire section specifically for parents with guidance, tips, and strategies for supporting your child’s emotional regulation journey……

    This Week Only: Our Gift to You

    Luis and I believe every family deserves access to understanding……

    That’s why this week (December 2-6), we’re offering the Kindle eBook version of “Autism: Calming the Chaos” completely FREE……

    Download your free copy here – Available Dec 2-6 only

    (You don’t need a Kindle device, the free Kindle app works on any phone, tablet, or computer!)……

    This is our thank you to this incredible community that has supported us, shared our books, and trusted us with their stories……

    If cost has been a barrier, now’s your chance. Download it. Share it with your child’s teacher. Send it to grandparents. Pass it along to anyone who needs to understand meltdowns better……

    Let’s spread understanding together.

    Beyond This One Book: Our Complete Journey

    “Autism: Calming the Chaos” is just one part of our family’s story……

    We’ve written an entire series based on Adrián and Guillermo’s real experiences, each book addressing different challenges we’ve navigated:……

    📚 Autism: Calming the Chaos – Understanding and supporting meltdowns (FREE this week!)

    📚 Autism: Confidence Starts Here – Building self-esteem and celebrating differences

    📚 Autism: A New School Year – Managing transitions and back-to-school anxiety

    📚 Autism: My Invisible Backpack – Understanding masking and emotional overload

    📚 Party Time for Adrián – Navigating social events with confidence

    Each book includes: ✓ Stories based on our real family experiences ✓ Beautiful hand-drawn illustrations ✓ Practical strategies you can use immediately ✓ Bonus sections for parents and educators ✓ Downloadable resources and tools……

    FREE Resources for Your Family

    Beyond our books, we’ve created tons of FREE downloadable resources to support your family:……

    Access all our free resources here

    You’ll find:

    • Meltdown prevention checklists

    • Visual calm-down strategy cards

    • Emotion identification tools

    • Social stories templates

    • Sensory regulation guides

    • And so much more, all completely free……

    Because we believe support should be accessible to everyone……

    The Community That’s Walked This Journey With Us

    Writing “Autism: Calming the Chaos” wasn’t just about our family’s story……

    It was inspired by every parent who’s messaged us saying “I thought I was alone.”……

    Every teacher who’s asked “How do I help this student?”……

    Every grandparent who’s said “I want to understand my grandchild better.”……

    Every autistic adult who’s shared “I wish someone had explained this to me when I was young.”……

    You’ve all shaped this book.

    Your questions. Your struggles. Your victories. Your wisdom……

    This community of families, educators, therapists, and autistic individuals navigating this journey together, that’s what gives this book its heart……

    What Parents Are Saying

    “This book is super helpful to any parent with an autistic child… beautifully illustrated, makes it more interesting to read and absorb the information.” — Phil_AE

    “My daughter recognizes Adrian in the illustrations already! It has allowed me to not only use the techniques ourselves as a family during a meltdown but to also understand other kids when they have one.” — Andre Cassis

    “A lifesaver for understanding my grandson’s autism… The practical tips for handling emotional crises have given me the confidence to know what to do if a meltdown occurs at home, park, school everywhere.” — Gloria (Spain)

    “Well-written book, well-illustrated, easy to read, and as someone with a neuroscience degree, I appreciated their understanding that it’s not the fault of the kid… very empathetic.” — Yair Aizenman……

    These reviews mean everything to us because they tell us: this is helping families. And that’s why we do this work……

    From Our Family to Yours

    That park floor moment I told you about at the beginning? It doesn’t haunt me anymore……

    Because now I understand what was happening. Now I know how to help. Now I have tools, and so does Adrián and Guillermo……

    Writing “Autism: Calming the Chaos” was our way of making sure other families don’t have to feel as lost as we once did……

    Every strategy in this book is something we’ve lived. Every insight comes from real experience. Every word is written with love for our boys and hope for your family……

    This week, it’s free. Not because we’re running a promotion, but because we genuinely believe every family deserves access to understanding……

    Download your free copy here (Dec 2-6 only)

    Share it. Use it. Let it help you the way writing it helped us……

    And if it makes a difference for your family? That’s all the thanks we need 💙

    With love, understanding, and solidarity,
    Dalisse & Luis
    Loving Pieces Books

    📧 Stay Connected:

    💙 Have you read Calming the Chaos? What resonated most with your family? Share your story with our community, we’re all learning together.

  • The Moment I Finally Understood: Meltdowns Aren’t Tantrums

    • by

    I used to think I was failing as a parent.

    Every time Adrián had what I called a “tantrum” in public, I felt the weight of judgmental stares. The whispers. The head shakes. The well-meaning advice: “You just need to be firmer with him.”

    And honestly? Part of me believed them. Maybe I wasn’t being firm enough. Maybe I was “giving in” too easily. Maybe I was doing something wrong.

    Then one day, our therapist said something that changed everything:

    “Dalisse, that’s not a tantrum. That’s a meltdown. And the difference matters more than you realize.”

    I sat there in her office, tears streaming down my face, because suddenly, finally…things started to make sense.

    Understanding the difference between meltdowns and tantrums literally transformed how Luis and I parent. It changed how we respond, how we prepare, how we feel about ourselves as parents.

    If you’ve been confusing the two, if you’ve been treating meltdowns like behavior problems, I want you to know: you’re not alone. And understanding this difference? It changes everything.

    The Day It All Clicked

    Let me tell you about the grocery store incident that finally made it all make sense.

    Adrián was 5. We were shopping for dinner, just a quick trip we did not plan and he had a long at school. Within minutes, he was on the floor, hands over his ears, screaming. People stared. Someone muttered “something something” An older woman actually came up to me and said, “Pick him up.”

    I picked him up, abandoned our cart, and carried him…still screaming to the car.

    I drove home feeling like the worst mother in the world. Why can’t I control my own child? What am I doing wrong?

    But here’s what I didn’t understand then: Adrián wasn’t trying to do anything. He wasn’t manipulating. He wasn’t being difficult. He wasn’t throwing a tantrum to get his way.

    His nervous system had hit complete overload.

    The fluorescent lights buzzing. The refrigerators humming. Five different food smells competing. A baby crying three aisles over. Shopping cart wheels squeaking. Strangers’ conversations bouncing off tile floors. I will never forget this how I felt, how I imagined my son felt … ufff 

    For his autistic brain, it all added up until there was nowhere for the sensory input to go except OUT, in the form of what looked like a “tantrum” but was actually a meltdown.

    What’s the Actual Difference? (And Why It Matters So Much)

    We explain this visually to Adri and Guille nos with our book Autism: Calming the Chaos it’s even easier. 

    Okay, let’s break this down in a way that finally made sense to me.

    Tantrums: Goal-Oriented

    What they are: A child’s strategy to get something they want or … avoid something they don’t want.

    What they look like:

    • Crying, whining, arguing
    • Stopping when they get what they want (or realize they won’t)
    • Awareness of their surroundings (watching to see if it’s “working”)
    • Some level of control over their behavior

    Example: Guillermo sees a toy at the store. I say no. He cries, begs, throws himself on the ground. When I stay firm and we walk away, he eventually stops and moves on.

    That’s a tantrum. He had a goal (get the toy), used a strategy (crying/begging), and when it didn’t work, he regulated and moved on.

    Meltdowns: Nervous System Overload

    What they are: An involuntary response to complete overwhelm, sensory, emotional, or cognitive.

    What they look like:

    • Total loss of control
    • Continuing even after getting what they “wanted”
    • No awareness of surroundings (they’re in survival mode)
    • Can’t stop even if they want to

    Example: Adrián at that grocery store. Even after we left (removing him from the situation), he couldn’t stop. In the car, he was still crying, still covering his ears, still completely overwhelmed. It took 20 minutes in a quiet, dark space for him to even begin to regulate.

    That was a meltdown. His nervous system hit overload. The thinking, rational part of his brain went offline. He wasn’t choosing anything, he was drowning.

    Why I Was Getting It So Wrong

    Here’s what was happening before I understood the difference:

    When Adrián had a meltdown, I would:

    • Try to reason with him (“Calm down, we’re leaving!”)
    • Feel frustrated that “nothing worked”
    • Worry I was being “too soft” by not punishing him
    • Feel embarrassed by the public spectacle
    • Question my parenting constantly

    All of that made everything worse.

    Because you can’t reason with someone in a meltdown. Their brain literally cannot process language when they’re in that state.

    You can’t punish someone out of a meltdown. That’s like punishing someone for having a panic attack, it doesn’t work and it’s not fair.

    And the embarrassment? That was coming from a fundamental misunderstanding of what was happening.

    What Changed When I Finally Got It

    Once Luis and I understood that meltdowns were neurological, not behavioral, everything shifted.

    We Stopped Trying to “Fix” the Behavior

    Before: “Adrián, you need to calm down right now. This is not acceptable.”

    After: “You’re safe. I’m here. Take your time.”

    We Started Preventing Instead of Punishing

    Before: Consequences after meltdowns, hoping it would “teach” him.

    After: Identifying triggers, avoiding overload when possible, building in breaks before meltdowns happened.

    We Changed Our Own Emotional Response

    Before: Frustration, embarrassment, feeling like failures.

    After: Compassion, understanding, knowing we were supporting our son through something really hard.

    The Triggers I Wish I’d Recognized Sooner

    Looking back, Adrián’s meltdowns almost always had clear triggers. I just didn’t know what to look for.

    Sensory Overload (The Big One)

    This was behind probably 70% of his meltdowns:

    • Loud or unpredictable noises
    • Bright or flickering lights
    • Strong smells
    • Crowds and chaos
    • Certain textures (tags in clothing, sticky hands)
    • Too much visual input

    The grocery store? Sensory overload central.

    Changes in Routine

    Autistic kids often thrive on predictability. When routines change unexpectedly—even small changes, it can trigger anxiety that builds into a meltdown.

    Taking a different route home. A substitute teacher. Dad leaving for work at a different time. Plans changing last minute.

    For Adrián, these felt destabilizing in a way I didn’t initially understand.

    Communication Frustration

    Imagine knowing exactly what you need but being unable to express it. Or expressing it repeatedly and no one understanding you.

    That frustration builds. And builds. And eventually explodes into a meltdown.

    Emotional Overwhelm

    Sometimes the emotion itself is the overwhelm, even positive emotions like excitement.

    Adrián has had meltdowns on Christmas morning. At birthday parties. During celebrations. Not because he was unhappy, but because the emotion was too BIG for his system to process.

    The “Accumulation Effect”

    This one took me forever to understand: sometimes the meltdown happens after the overwhelming thing.

    Adrián would hold it together all day at school, managing all the sensory input, social demands, and schedule changes. Then he’d come home and completely fall apart.

    I used to think, “Why is home the place he loses it?” But a therapist explained: home is his SAFE place. He held it together where he had to, then released it where he felt secure enough to let go.

    That’s not a problem. That’s actually healthy.

    What Actually Helps During a Meltdown

    Okay, this is the practical part. What do you actually DO when your child is in a meltdown?

    Priority #1: Safety

    Make sure they can’t hurt themselves or others. That’s it. That’s the first job.

    Move sharp objects. Block stairs. Stay close enough to intervene if needed. But don’t crowd them unless they want physical comfort.

    Lower the Sensory Input

    If you can:

    • Move to a quieter space
    • Dim the lights
    • Reduce noise
    • Remove crowds
    • Offer headphones or a weighted blanket

    Even if you can’t change the environment, removing your child from it can help.

    Minimize Talking

    I know your instinct is to explain, reassure, problem-solve. Mine too.

    But during a meltdown, their brain can’t process language. Too many words = more overwhelm.

    Keep it simple:

    • “You’re safe.”
    • “I’m here.”
    • “Take your time.”

    That’s it.

    Give Space (But Stay Present)

    Some kids need physical comfort during meltdowns, Luis can hug Guillermo and it helps him calm.

    But Adrián needs space. If we touch him during a meltdown, it makes it worse.

    Learn what YOUR child needs. And respect it, even if it’s not what you want to give.

    Remember: This Will Pass

    In the moment, meltdowns feel endless. But they do end. Your job isn’t to stop it, your job is to keep them safe while their nervous system resets.

    What Comes After: The Recovery Phase

    Once the meltdown is over, your child will be exhausted. Think about it, they just had the neurological equivalent of running a marathon.

    What helps:

    • Quiet time with no demands
    • Comfort (if they want it)
    • Maybe a preferred activity
    • Definitely no lectures or “talks about what happened”

    There’s a time for reflection and learning, but it’s NOT immediately after a meltdown.

    Luis and I wait until Adrián is fully regulated, usually hours later, sometimes the next day, before we gently discuss what happened and what might help next time.

    The Guilt I Had to Let Go Of

    Here’s something nobody talks about: the guilt.

    I felt guilty every time Adrián had a meltdown. Like I should have prevented it. Like I should have known better. Like I was failing him.

    But here’s what I’ve learned: you can’t prevent all meltdowns.

    Even with the best preparation, best strategies, best understanding, sometimes the world is just too much. And that’s not your fault. It’s not your child’s fault. It’s just… reality.

    What you CAN do:

    • Recognize triggers and minimize them when possible
    • Build in preventive breaks
    • Create safe spaces for regulation
    • Respond with compassion instead of punishment
    • Learn and adjust as you go

    That’s not failing. That’s parenting an autistic child with love and wisdom.

    For the Tantrums (Yes, Autistic Kids Have Those Too)

    Let me be clear: autistic kids can have tantrums AND meltdowns. They’re not immune to typical childhood behavior.

    Guillermo absolutely throws tantrums when he doesn’t get his way. And we handle those differently than meltdowns.

    For tantrums:

    • Stay calm but firm
    • Set clear boundaries
    • Don’t give in to the behavior
    • Offer choices when appropriate
    • Follow through with consequences if needed

    The key: During a tantrum, they’re still in control. They’re testing boundaries, expressing frustration, trying to influence the outcome.

    During a meltdown, they’re NOT in control. They’re drowning.

    Different situations require different responses.

    What I Wish Every Parent Knew

    If you take nothing else from this post, please hear this:

    Meltdowns are not bad behavior. They’re communication.

    They’re your child’s nervous system saying, “I’ve hit my limit. I need help.”

    When you respond with understanding instead of punishment, with compassion instead of frustration, everything changes.

    Not just for them, for you too.

    Because parenting from a place of understanding feels so different than parenting from a place of shame and confusion.

    Resources That Actually Helped Us

    If you’re looking for more support in understanding meltdowns and how to respond, here’s what genuinely helped our family:

    📚 Autism: Calming the Chaos – This is the book Luis and I wrote specifically about meltdowns. It’s told from Adrián’s perspective and includes strategies that have actually worked for our family.

    And we’ve created FREE downloadable resources including:

    • Meltdown vs. Tantrum comparison chart
    • Trigger identification worksheet
    • Early warning signs checklist
    • Calm-down strategies cards

    That grocery store meltdown I told you about? It doesn’t haunt me anymore.

    Because now I understand what was really happening. Now I know Adrián wasn’t being difficult… he was struggling. And now I know how to help.

    You can get there too. Understanding is the first step. Compassion is the second. And practical strategies? Those come with time and practice.

    You’re not failing. You’re learning. And that’s exactly what your child needs you to do.

    With understanding and solidarity,
    Dalisse (& Luis)
    Loving Pieces Books

    💙 Have you had a moment when understanding meltdowns vs. tantrums changed how you parent? What was your “aha” moment? Share with our community—we’re all learning together. Find us on Instagram @lovingpiecesbooks or explore more resources at lovingpiecesbooks.com.

     

  • The Day I Realized I’d Been Searching for the Wrong Kind of Help

    • by

    For the first two years after Adrián’s diagnosis, I devoured every autism resource I could find.

    Books. Websites. Expert advice. Therapy techniques. Evidence-based strategies.

    And you know what? I felt more lost than ever.

    Because all of it, ALL of it… felt clinical. Detached. Like it was written by people studying autism from the outside, not living it from the inside. It used big complicated concepts that between my sadness and my willingness to learn it was getting to much to gasp.

    Apart that none of it felt like us. None of it understood what our actual days looked like. The messy, beautiful, overwhelming reality of raising autistic kids.

    Then one day, I stumbled into an online group of autism parents, real parents, sharing real stories. No jargon. No clinical distance. Just: “Here’s what happened today. Here’s what worked. Here’s where I’m struggling.” Reddit did the trick.

    And for the first time since Adrián’s diagnosis, I felt like I could relate. Of course I am grateful for the professionals who guide us every day up to this day, but I felt I needed to see and hear from other parents too.

    That’s when my real autism parenting journey began. Not when I got the diagnosis. Not when I read all the books. But when I found community, and realized I wasn’t alone.

    If you’re reading this feeling overwhelmed, confused, or like you’re the only one who doesn’t have it all figured out, I see you. And I want you to know: you’re not alone. Not even a little bit.

    The Journey I Didn’t Expect

    Let me be honest about something: I thought an autism diagnosis would come with a roadmap.

    Like, here’s the diagnosis, here are the next steps, follow this path, and everything will be okay.

    Spoiler alert: That’s not how it works.

    Instead, it felt like being dropped in the middle of a forest with no map, no compass, and everyone around you speaking a language you don’t understand.

    IEPs. Sensory diets. ABA. OT. Speech therapy. Social skills groups. Developmental milestones. Red flags. Early intervention.

    The terminology alone was overwhelming. And underneath all of it was this constant, gnawing fear:

    Am I doing this right? Am I doing enough? Am I somehow making it worse?

    The Moment That Changed Everything

    Adrián was 6. We were sitting with luis listing all the things he “couldn’t” do.

    Can’t maintain eye contact.
    Can’t handle transitions.
    Can’t regulate his emotions.
    Can’t, can’t, can’t.

    I felt myself shrinking with every word. Like my beautiful, curious, creative son was being reduced to a list of deficits.

    Then Luis, my rock, my partner who always sees things more clearly than I do, spoke up:

    “Can we talk about what he can do? Because Adrián can name every Train Station in Spain in chronological order. He can draw the most intricate Road structures I’ve ever seen. He can tell you exactly how he’s feeling when he has the right words. He can do so many incredible things.”

    Then we actually smiled.

    “You’re right,” I said. “Let’s start there.”

    That was the day we stopped focusing on fixing Adrián and started focusing on supporting him to be the best version of himself.

    What “Support” Actually Looks Like (Hint: It’s Not What I Thought)

    I used to think supporting Adrián meant making him more “typical.”

    Helping him make eye contact. Teaching him to sit still. Getting him to stop stimming. Making him fit in.

    God, I cringe thinking about that now.

    Because here’s what I’ve learned: support doesn’t mean changing who your child is. It means giving them tools to navigate a world that wasn’t designed for them.

    The Visual Schedules That Saved Our Mornings

    Mornings used to be chaos. Pure, tear-filled chaos.

    Adrián would melt down almost every school morning because he couldn’t predict what was coming next. The uncertainty felt overwhelming.

    Then our OT suggested visual schedules. Simple picture cards showing the morning routine:

    1. Wake up
    2. Get dressed
    3. Eat breakfast
    4. Brush teeth
    5. Put on backpack
    6. Get in car

    Game. Changer.

    Suddenly, Adrián could see what was coming. He could prepare himself. The meltdowns didn’t disappear completely, but they decreased dramatically. We are using this more and more with Guillermo and he loves this!

    It wasn’t about changing him. It was about giving him a tool to manage something that was genuinely hard for his brain.

    The Sensory Tools That Made Public Spaces Bearable

    For years, we avoided places that were too loud, too bright, too crowded. Which meant we avoided a lot of life. Adrián did not mind the loud noises but he disliked crowded places, so we avoided them as much as we could.

    Guillermo has a hard time with noises and when we discovered noise-canceling headphones.

    Such a simple thing. But it transformed Guillermos experience of the world.

    Suddenly, he could go to school assemblies. Birthday parties. Family gatherings. The grocery store didn’t trigger immediate meltdowns.

    By boys are still autistic. They will still processed sensory input differently. But now we had a tool that helped Guillermo manage Loud noises, and we know to avoid crowded places for Adri to stay regulated.

    That’s support. Not changing who they are, but equipping them to participate in life on their own terms.

    The Social Stories That Built Understanding

    Adrián struggles with understanding unspoken social rules. Things neurotypical kids just… absorb? He needs them explained explicitly.

    So we started using social stories, simple narratives that walk through social situations step by step.

    “When we go to Grandma’s house, she might want to hug you. You can say ‘I’d rather do a high-five’ if hugs feel uncomfortable. That’s okay.”

    “At the park, if you want to play with someone, you can say ‘Can I play too?’ They might say yes, or they might say no. Both answers are okay.”

    These stories gave Adrián a framework for navigating social situations that felt confusing and unpredictable.

    Again, not changing him. Giving him tools.

    The Community That Became My Lifeline

    Here’s something they don’t tell you about autism parenting: the isolation is crushing.

    Even when you’re surrounded by people who love you, you can feel completely alone. Because they don’t get it.

    They don’t understand why you can’t just “make” your child behave.
    They don’t get why a birthday party feels like a military operation requiring days of preparation.
    They don’t know what it’s like to celebrate victories like “He wore jeans today!” while other parents are celebrating scholarships and sports trophies.

    I needed people who got it. And I found them online.

    The Facebook Group That Saved My Sanity

    I joined an autism parenting group when Adrián was 5, mostly just to lurk. I wasn’t ready to share my story yet.

    But reading other parents’ posts? Life-changing.

    “My son had a meltdown at Target today and I sat on the floor with him while people stared. I’m exhausted but I know I did the right thing.”

    “Small victory: She tried a new food today! Just a tiny bite, but I’m counting it as a win.”

    “Does anyone else’s kid line up all their toys in perfect rows? Is this normal?”

    Reading these posts, I realized: I’m not alone. Other people understand. This is hard, but it’s not just hard for me.

    Eventually, I started commenting. Then posting. Then forming real friendships with parents across the country who “got it” in a way my IRL friends couldn’t.

    That community became my lifeline.

    The Autistic Adults Who Taught Me Everything

    But here’s the thing: parent groups are crucial, but they’re not enough.

    The people who taught me the MOST about autism? Autistic adults.

    Following actually autistic people on social media opened my eyes in ways no parenting book ever could.

    They explained what stimming feels like from the inside.
    They described why eye contact is uncomfortable.
    They shared what masking costs them.
    They talked about what they wish their parents had understood.

    Listening to autistic voices transformed how I parent.

    And here’s a full-circle moment: years later, I discovered I’m autistic too. Late-diagnosed at 39, after my boys’ diagnoses prompted me to recognize myself in their experiences.

    Suddenly, so much of my own childhood made sense. The overwhelm. The masking. The feeling of being different but not knowing why.

    Understanding my own autism made me a better parent to my autistic kids.

    The Strategies That Actually Work in Real Life

    Okay, let’s get practical. Because understanding and community are crucial, but you also need tools for the day-to-day.

    Emotion Regulation Tools

    Both Adrián and Guillermo struggle with big emotions. When they’re upset, they can’t just “calm down” on command.

    What helps:

    Visual emotion charts – Pictures showing different feelings. Both boys can point to how they’re feeling when words are too hard.

    Calm-down corner – A designated space with dim lighting, soft textures, weighted blankets, and favorite comfort items. No punishment, just a safe place to regulate.

    Breathing exercises – We practice these when they’re calm, so the technique is familiar when they need it. Deep breath in for 4, hold for 4, out for 6.

    Sensory tools – Fidget toys, chewable necklaces, therapy putty. Different kids need different input.

    Building Independence Through Choice

    Autistic kids often feel like life happens to them, they have little control over their days, their schedules, their experiences.

    Giving choices: even small ones, builds confidence and autonomy.

    “Do you want to wear the blue shirt or the red shirt?”
    “Should we read two books or three books tonight?”
    “Do you want a snack now or after your shower?”

    These aren’t big decisions. But they give Adrián and Guille practice in self-advocacy and decision-making.

    Celebrating Progress, Not Perfection

    This one is hard for me. I’m a perfectionist by nature, and I had to actively retrain my brain to celebrate small victories.

    Adrián tried a new food? WIN.
    Guille used words instead of screaming when he was frustrated? WIN.
    We made it through a family gathering without a meltdown? HUGE WIN.

    I keep a “wins journal” where I write down these moments. On hard days, I flip through it to remind myself: we are making progress. It just looks different than I expected.

    The Books That Became Tools, Not Just Stories

    When Adrián was struggling with confidence, feeling different, wondering if anyone else felt like him, I searched desperately for books where he could see himself.

    Books that didn’t treat autism like a tragedy. Books that celebrated neurodiversity. Books written by people who actually understood.

    We did find some good ones but not as many options as other children’s book. So Luis and I created them.

    Autism: Confidence Starts Here was born from watching Adrián struggle with self-esteem. From hearing him say “Why am I different?” and wanting to show him that different is beautiful.

    Autism: Calming the Chaos came from our meltdown struggles. From wanting to help Adrián understand what was happening in his body, and help other families respond with compassion instead of punishment.

    Autism: My Invisible Backpack addresses masking and emotional overload, things I didn’t even have language for until my own diagnosis.

    These aren’t just books we wrote. They’re tools our family uses. Adrián rereads them when he’s struggling. They’re conversation starters. They’re validation.

    That’s what I was searching for all those years ago. Stories that understood.

    What I Wish Someone Had Told Me

    If I could go back and talk to myself the day Adrián was diagnosed, here’s what I’d say:

    1. The grief is real, and it’s okay.

    You’re allowed to grieve the future you imagined. That doesn’t mean you don’t love your child. It means you’re human.

    2. Your child is not broken.

    They don’t need to be fixed. They need to be understood, supported, and celebrated for exactly who they are.

    3. You will make mistakes.

    You’ll say the wrong thing. Use outdated terminology. Push when you should have pulled back. It’s okay. Learn and adjust.

    4. Find your people.

    The parents who get it. The autistic adults who can teach you. The therapists who see your child as whole. Build that community intentionally.

    5. Trust your instincts.

    You know your child better than any expert. If something doesn’t feel right, speak up. Advocate. Push back.

    6. Celebrate differently.

    Your milestones might not match other families’. That’s okay. Every step forward, no matter how small, deserves celebration.

    7. Take care of yourself.

    You can’t support your child from a place of depletion. Rest. Ask for help. Let some things go.

    8. It gets easier.

    Not because autism goes away, but because you learn. Your child learns. You develop systems. You find your rhythm.

    9. Your child is amazing.

    Not despite being autistic. Not even because of it. Just… inherently, wonderfully, perfectly amazing as they are.

    The Journey Continues

    Adrián is 11 now. Guillermo is 5. Our journey is far from over, it’s really just beginning in so many ways.

    But we’re not where we were six years ago, drowning in confusion and fear.

    Now we have tools. Community. Understanding. Hope.

    We know Adrián’s triggers and how to support him through overwhelm.
    We’ve built routines that work for our family’s unique needs.
    We’ve connected with other families who get it.
    We’ve learned to celebrate our wins… even the tiny ones.

    And most importantly: we’ve learned to see autism not as something to overcome, but as a different way of being that deserves respect, support, and celebration.

    Resources for Your Journey

    If you’re looking for support on your autism parenting journey, here’s what has genuinely helped our family:

    We’ve created FREE downloadable resources including:

    • Visual schedule templates
    • Emotion regulation tools
    • Social story frameworks
    • Sensory profile worksheets

    You’re on that journey too. And you don’t have to walk it alone.

    With solidarity and hope,
    Dalisse (& Luis)
    Loving Pieces Books

    💙 What’s been your biggest “aha” moment on your autism parenting journey? What do you wish you’d known sooner? Share with our community, we’re all learning together. Find us on Instagram @lovingpiecesbooks or explore more resources at lovingpiecesbooks.com.

  • Today’s Mantra: Lower the Bar, Find the Joy. You’re Doing Great.

    • by

    Today’s Mantra: Lower the Bar, Find the Joy. You’re Doing Great.

    If you’re feeling a quiet sense of dread mixed with the holiday excitement, you’re not alone. Thanksgiving can feel like the ultimate test for autism families, a day packed with sensory landmines, social expectations, and the pressure to create “perfect” memories.

    This year, I’m inviting you to a different kind of celebration. One where the goal isn’t a flawless turkey or a seamless family photo. The goal is connection. The goal is joy. And sometimes, the only way to find it is to gently, lovingly, lower the bar.

    Release the Grip of the “Perfect” Day

    I remember a Thanksgiving where I spent hours orchestrating the perfect, quiet, low-stimulation dinner. I had a schedule, safe foods, and escape plans. And then, my son, overwhelmed by the new smells, spilled an entire glass of sparkling cider right onto the “safe” plate.

    In the stunned silence, I took a breath. And then, I did something unexpected: I laughed. A real, from-the-gut laugh. He looked at me, wide-eyed, and a tiny smile touched his lips. That messy, imperfect moment, not the perfectly browned turkey, is the one I remember with a warm heart. It was the moment we connected.

    What helps us: Let go of the script. The most beautiful moments are often the unplanned ones. If the turkey is dry but your child is smiling, the day is a success.

    Celebrate the Quiet Victories

    While others are counting calories or football scores, let’s count our own unique wins.

    • Did your child tolerate the smell of pumpkin pie for a few minutes? That’s a win.

    • Did they use a new sign or word to ask for more mashed potatoes? That’s a win.

    • Did you manage to take five deep breaths in the bathroom instead of yelling? That’s a huge win.

    These are the real milestones. They may not make the family newsletter, but in our homes, they are everything. Shifting our focus to these small sparks of joy builds a foundation of gratitude that is deep, real, and resilient.

    Find Your Feast of Connection

    The feast isn’t just on the table. It’s in the moments we truly see each other.
    Maybe your Thanksgiving looks like snuggling on the couch with a favorite book instead of sitting at the loud, crowded table.

    Maybe it’s a walk outside, crunching leaves and pointing at clouds, away from the overwhelming chatter.
    Maybe it’s ordering pizza and being profoundly, gratefully, okay with it.

    Your version of Thanksgiving is valid. It is enough. It is beautiful.

    This holiday, I am so deeply thankful for you, for showing up, for trying again, for loving your child in all the ways that matter. You are not just building a Thanksgiving menu; you are building a world where your child feels safe, seen, and loved.

    And that is everything.

    Happy Thanksgiving, from our imperfect, grateful family to yours.

    With love and solidarity,

    Adrián, Guillermo, Dalisse and Luis

    The Loving Pieces Books Family