Hilary Duff knows a thing or two about dreaming big. The former child star (Disney’s Lizzie McGuire) is also a singer, businesswoman, mother and New York Times best-selling author!

A mother of three, including recent addition Mae, Duff just released a new book, My Little Brave Girl ($11.73). It’s a sweet bedtime read encouraging young girls to reach high, dream bigger and approach the world with their hearts wide open. Published through Penguin Random House, it’s Duff’s first foray into the world of children’s books.

My Little Brave Girl cover
Like many good children’s books, this one is inspired by Duff’s own experience as a mother as she considers all the ways her daughter is brave. It’s a timely message of empowerment and confidence and it’s beautifully illustrated with diverse characters. Although it’s marketed for children ages 3-7, its messaging will resonate with any girl or woman facing a new challenge or opportunity.

My Little Brave Girl is available everywhere that books are sold and would make a perfect last-minute Mother’s Day Gift. It’s also available as an audiobook from the Listening Library, read by Duff herself. Pick a copy up and get ready to feel inspired!

—Sarah Shebek

Featured image courtesy of Penguin Random House 

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Our daughter is 3 years old and was just recently diagnosed with autism.

This came with so many emotions, but the one I felt the most was peace. Finally, we knew. We were finally out of the unknown and we could move forward! It’s like I had a backpack on, and someone took out a bunch of rocks. I felt free. It was empowering. But, the road before her diagnosis was dark.

When you know something is wrong and you can’t fix it, as a parent it’s debilitating. It makes you feel so lifeless and weak because you can’t figure out what’s wrong. And doctors are great too, but they can only recommend so many things, cross off their lists, and ultimately, it’s not their child. It’s yours.

I felt so alone. I felt like no one in the whole entire world had ever gone through this. I had an aching in my heart for my daughter, Opal. I wanted to help her, but I didn’t know how.

That unknown area is the hardest. I was stay at home mom and it felt like it was my fault that my child wasn’t on the same level as all her peers. It was hard to celebrate other children’s victories when my child couldn’t relate. And the questions. Everyone asks why your child isn’t talking or if they know the alphabet or their colors, when I’m struggling to even get my child to eat food with some kind of nutritional value.

If you’re on that middle road right now, I want to encourage you. It’s not your fault. You are an amazing parent. Your child is amazing. You are not alone.

My heart goes out to you. I know how you’re feeling. I know the pain. I know the heartbreak. It’s one of the worst feelings ever. But, hang in there. You may feel like you want to raise your white flag and escape it all, but you have a child who needs you. You don’t have to pretend you’re strong or put on a brave face, but you do have to keep moving forward. Cry, let out your emotions, don’t bottle them up. But once you’re through, hike up your momma leggings, and fix that cape. You can do this. I’m rooting for you!

Hi! I'm a wife and mom to two beautiful girls! I have a three year old, Opal, and a one year old, Lucy. My oldest was just diagnosed on the Autism Spectrum. I love to watch reruns of "FRIENDS" and drink chai tea whenever I have a free second!

Photo: Victoria Rosenberg

I’ve thought about writing this out a thousand times.

And I’ve tried to, just about as often. Writing is how I process and share. Over the past few years, reading the stories and experiences of others, whether through blog posts or Instagram captions, has changed my life. I know that sounds dramatic, but so be it. 

At first, in the early days after my son’s diagnosis, I couldn’t write and share because it would make it too real. It wasn’t the endless assessments and specialist appointments and forms to fill out, but seeing my own words, my own experience written out—it was too much. I also struggled with the fact that this is my son’s story. I am a supporting cast member, one who will never be able to understand his daily struggles, the amount of work and effort required to do what others consider simple daily tasks. That this is his story to share when, hopefully, he is one day able to. Who am I to broadcast his diagnosis and daily life to the world?

Who am I? I’m his Mom. His advocate. His haven. The second I saw the positive on the pregnancy test. The first ultrasound where this little bean on the screen was floating around. The first flutter. The first second after the doctor placed him on my chest in the delivery room and I didn’t know what else to say but to introduce myself as his Mommy and tell him how much I absolutely love him. Twenty months later, I sat in the developmental pediatrician’s office, listening to her relay what I had been trying to bring to the attention of everyone for months. Then she spoke the words that confirmed everything I already knew. The first (and likely last) time I hated being proven right.

I told myself over and over again that just because he now had the diagnosis of Autism Spectrum Disorder nothing changed. He was still the exact same amazing little boy that he was seconds before the doctor had said the words out loud. We stepped outside and the sky was still blue, people continued along their day and other than the fact that the questions in my heart now had answers and the doubt was replaced by fear, life continued on. Four and a half years later and I’ve remained a spectator to the stories of others. I devour blog posts and articles, Instagram accounts dedicated to the lives of other families going through similar journeys to ours and anything I can find. I crave community and the ability to say, “us too!” but never put myself out there.

Recently in the middle of meltdowns or IEP meetings or while consulting with therapists, when I feel like no one else understands, I’ve come to discover it’s because of me. How could anyone else ever understand us when I don’t share? When I don’t offer my story or my experiences? I’ve only been more than happy to sit back and benefit from those brave families who do share. So while this is his story and I will never, ever even attempt to speak for him, my brave and incredible son, who I am so in awe of every single day, and what it means to be him, it’s also a part of my story.

This is for those Moms who just received their child’s diagnosis and aren’t ready to open up but desperately need to know they aren’t the only ones in the world with this new journey ahead of them. I’m adding my voice to the ring and to let you know you aren’t alone. While our children have endless people entering their lives now in the form of specialists, therapists, teachers, doctors and more, and while the spotlight is rightfully shone on them as they begin to navigate their way through supports and programs with you by their side, the need for a community for us—the caregivers, parents, and siblings—is just as important.

Whether you find that community in your neighborhood, on Instagram or through posts like this one, find it and hold on to it. I won’t end this with one of the trillion things people always feel compelled to say upon learning of a diagnosis, I won’t even say I understand because my son’s Autism is not your child’s Autism. All I’ll say is that you’re not alone because sometimes that’s really all we need to hear. 

This post originally appeared on Itsy Bitsy Balebusta.
Victoria Rosenberg
Tinybeans Voices Contributor

I usually go by Mommy, but you can call me Victoria! I have two sons and a daughter and spend my days navigating the adventures of motherhood! With a focus on special needs, I hope to help those who feel alone or overwhelmed, find their village!

LEGO wants to help your little adventurer celebrate International Women’s Day with a very special deal! The new Amelia Earhart Tribute set is here—and it’s free with any purchase over $100.

You read that right. LEGO wants to gift your master builder with their very own brick version of Earhart’s Lockheed Vega 5B plane. The 203-piece set is age-graded for children ages eight and up and includes a mini figure of the aviator herself.

photo: LEGO

Mel Caddick, the designer behind the new set, said in a LEGO Q&A, “Amelia Earhart taught us that passions, aspirations and courage know no gender—a legacy not passed on by many, and for that I think we found the perfect personality to celebrate for 2021 International Women’s Day.” Caddick went on to talk about what people can learn from this model, “I am hoping the model of Amelia Earhart can inspire and encourage, not only women, but all people around the world, to be curious and brave about their passions and aspirations—especially when facing rigid traditions, structures or the likes, that tries to keep them down.”

Visit LEGO’s website here to learn more about the free (with $100 or more purchase offer). Don’t wait to order your kiddo’s Earhart-themed set. This offer is only good through Mar. 14. If you order after the free offer period or you don’t purchase $100 worth of other LEGO items, you can buy the set for $19.99.

—Erica Loop

 

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mom and son in a field

Photo: Laney Photography

About two years ago my son and I were waiting in line at Walmart. He was sitting in the cart happily flapping and stimming as we waited. A lady, waiting in line behind us, started talking to him. When he didn’t respond I explained to her that he was non-verbal and on the autism spectrum. She immediately proceeded to thank me and tell me how great it was that I wasn’t ashamed to bring him out and about in the community.

I will never be ashamed that my son has autism. It’s one of the many parts of him that contribute to making him the amazing little boy that I love and adore.

No one could ever take over the space in my heart that he fills with his spins, squeals, smiles, jokes, and flaps. These things are mixed in amongst deep love, hope, and faith.

There is no room for shame here.

I’m not ashamed of autism and you shouldn’t be either because it’s not about a diagnosis.

It’s about the person.

My son brings so much more to this world than autism. He is smart, funny, charming, handsome, witty, kind, brave, loving.

I would hate for anyone to miss out on the positive bright light that he shines because they are consumed by the negatives.

Don’t miss out on something that could be amazing just because it could also be difficult.

Autism may look hard and challenging on the outside but he lives it every day from within.

Why would I punish him with shame for a life circumstance that he has absolutely no control over?

I will always take my son into the community. I will always encourage and support him. I will always hope for progress for him. I will always advocate for him. I will always walk beside him. I will always be his dance partner even when there is no music. I will always ensure that he is treated with respect and dignity because he is a human being and deserves to be treated as such.

As I watch this bright, brave boy climb mountains and shatter all the naysayers, I feel nothing but pride and gratitude because he’s mine and I am blessed beyond measure to be his Mama.

 

This post originally appeared on Stalen’s Way Facebook page.

I am a proud wife, ASD Mom, Step-Mom. At 21 months, my son was diagnosed with autism spectrum disorder. He is 5 years old and non-verbal. I have become a full-time stay-at-home mom. I am 1000% focused on raising autism awareness and helping my son live a full and fun life. 

Different not less. Let those words sink in for a moment. This small phrase has a large meaning in the autism community. For some, including myself, it has become a mantra, a mission if you will. I share our story simply so you can see this phrase lived out in real-time. Our journey may look and be different, but it is not less in any way, and never will it be.

Unfortunately, there are people who see this phrase and add the word “and” to it: “Different AND less.” They may not say it out loud, but their actions speak louder than words. And the story below is an unfortunate example of this. As a special needs parent, one of the biggest things I worried about at the beginning of this journey was if my child would be accepted for who he is. Will he have friends? Will people see him, the true him, even in the peak of our hard? Or will he be judged? Given up on? Labeled? I was lucky enough for that worry to be put right to bed because from the first moment my son’s therapies started, I knew my son was accepted. And man, did I sleep easier at night!

For the past two years, I’ve been lucky enough to live in this wonderful bubble—where acceptance is given and not earned. Where judgment ceases to exist. Where support is given freely even in the hardest of times. But my days in this wonderful bubble are quickly coming to end. As you continue on this journey, the inevitable happens, and the time comes for you to have to leave your safe space, your little bubble. You come to terms with having to leave the place and the people that love your child the most. The only place besides your village that understands the phrase “Different not less.”

Many parents start to lose that sleep again. All of that worry and those questions of acceptance that you asked yourself at the beginning of the journey start to creep back. And unfortunately, it’s because you hear and see stories like this below. People that should be a parent and child’s safe space, end up treating a child less because they are different. The story below happened in a friend’s own backyard. It tells a story that we as a special needs community wished was fictional, but know all too well exist and is most times even covered up. In this incident, a child’s aide stapled a piece of paper to the child’s head to serve as a reminder for the child to bring his water bottle to school. Yes, unfortunately, you read that correctly. What’s even worse is that when the mother brought this to the school’s attention, it was downplayed. Statements made as if, even true would make this situation okay: The paper was stapled to the child’s hair, not his head. The aide has had a clean record up until this point. There was no “intent to harm.” The aide wasn’t even fired, just written up and moved to a different classroom. It’s these incidents that make me realize that special needs individuals are seen as different and less. And that is truly heartbreaking.

I myself am a licensed Cosmetology Educator. Although I teach adults, the goal as a campus is to create a safe space for all our students. Backgrounds may be different, lifest‌yles may be different, learner types may be different, but what we all share in common is our love for the beauty industry. I would like to think that the same mindset would be true for teachers, school administrators, and aides but unfortunately, it seems we are hearing more and more of incidents like this happening.

So I ask you: When is enough going to be enough? When are people that treat special needs individuals less than going to be held accountable before a mom has to lose it on the entire school system? But more importantly, when are people going to start speaking up when they see someone that is different treated less? How many times does someone have to be made fun of or treated poorly before you say enough is enough? When do you draw the line? The special needs community needs everyone’s help when it comes to this.

Let’s be honest, the world needs everyone’s help when it comes to this. I don’t know about you, but the world my kids live in now is scary. It’s filled with hate and judgment and people thinking their way is the right way. Do you know one thing that will always be right? Treating everyone with respect and dignity. Special needs or not. And it seems like these days, this is not even something everyone can agree on. So until then, I’ll keep using my voice, I’ll stand side by side with the moms that are made out to look crazy because they demand their kids be treated equally, and I’ll keep speaking up when I witness different people being treated as less.

I’ll leave with this quote from Mother Teresa: “I alone cannot change the world, but I can cast a stone across the waters to create many ripples.” Are you brave enough to cast that stone when you see someone that is different treated less? As a mother of a special needs child, I hope that you can be. I need you to be. Because those ripples you create can positively impact our world. And I know so many brave individuals that do their best every day to navigate a world not made for them. The least we can do is be that stone for them. Create those ripples. That’s what I intend to do. I’ll continue to cast stones. I’ll continue to make ripples. And my hope is that one day, with your help, those ripples can turn into waves. 

This post originally appeared on Adventures in Autism with Murphy.

Shannon is a proud boy mom, Hairstylist, and passionate Autism Advocate. She lives in New Orleans, Louisiana with her two sons Murphy (5) and Merrick (2).  Murphy was diagnosed with Autism at the age of 3. Follow her family as they journey through Autism together on Adventures in Autism with Murphy Facebook and Instagram page. 

Is your daughter (or the growing girl in your life)…1. NEVER confident? 2. SOMETIMES confident? or 3. ALWAYS confident?

If you are like most parents, teachers, and girl champions today, you will likely see that she is wavering between numbers 1 and 2, unlikely to be anywhere near number 3. I am so curious why girls seem to be confident until around age 8 or 9. Then, their confidence wanes, enormously. What happens? Where does this confidence go? And, most importantly, how do we work together to build and boost her self-confidence?

What Is Confidence? 
Put simply, confidence is feeling strong and secure in yourself and your abilities and knowing you are capable of developing even more of your skills and talents to become even more confident. Why does confidence matter? Confident girls feel more happy and healthy. They are much more willing to take risks and show their bravery and adapt to changes. The most confident girls I know don’t spend a lot of time on their devices, they are engaged and involved in many different activities, and they don’t seem to care about what others think of them. Refreshing but rare.

Why Does a Girl Seem to “Lose” Her Confidence as She Grows? 
Girls seem to lose their confidence in a “perfect storm” of changes as they grow. They begin to have an awareness of how they compare to their peers and they start to evaluate (am I taller, smaller, smarter, less smart, as popular, not as popular, prettier or less pretty than so and so?). At the same time, their bodies start to change (at different rates, of course), their thinking becomes more shaped by their perception of how others seem them, and they are sensitive to what others think of them. Since they also need to gain peer acceptance (and fear judgment, criticism, and, ultimately, rejection) they change themselves to fit in. So, it’s no wonder they hold back and shy away from bravery, morph themselves into who others want them to be, and diminish their uniqueness. And, at the very seem time, they have 24/7 access to something called social media—perfected and polished images for them to see and though they love their phones, they do not realize how this is damaging their self-confidence and feelings of “not good enough.” 

Do you see how it is no wonder her confidence diminishes?

How Do We Work Together to Build & Boost Her Confidence? 

​​​​​​​Here are my top 6 tips to help you get started:

1. Be a positive power of example to her: you can tell her to “be confident” but more helpful, you will have to show her how it’s done —with your words—how you speak to yourself and also to others (and about others), with your body language—posture is everything, and with your actions, challenging yourself to speak up when you have been wronged and taking chances that may make you feel uncomfortable. 

2. Together, find examples of confidence in the girls she may be following online or watching on Netflix: talk about why they seem confident and if she is willing to try to emulate these girls in any way. What about Malala Yousafsai, Zendaya, Greta Thunberg, or any of the girls from the Babysitter’s Club Netflix series? Help her find and follow girls who are taking big steps, breaking glass ceilings, speaking up and out, making a difference, and shaping our world.

3. Practice how she speaks: words are EVERYTHING. First, to herself. Instead of, “I am just not good at reading”, ask her to try, “I am working hard on my reading skills and improving every day.” Then, with others. Instead of “I kind of think I might want to try a new restaurant for dinner”, ask her to say, “I would like to try a new restaurant” —clear and concise!

4. Work on her body language: essentially, this can help her feel more confident from the inside out but it also can show others she believes in herself. Body language includes: standing tall, chin out, shoulders back, and good eye contact. Practice makes progress (especially when it comes to muscle memory).

5. Finally, work on her skillset: I promise you, the more competent she feels the more confident she can feel too. To start, ask her what skills and talents she already has (girls tend to discount and discredit the work they have already achieved) from being a good friend, creating videos on Tik Tok, or being your sous chef. Then, ask her what skills she wants to develop—come up with a broad and expansive list that could include: learning to bake or cook; adventuring with hiking, biking, or swimming; starting a group for a fundraiser for the food bank or an environmental club. After all, we want our girls to be “all-rounders.” 

6. Teach her to be brave: taking risks—whether this is making a new friend, ordering for herself at Starbucks, or trying new activities is never easy—and you may need to do this in tandem. Break new skills into small acts of micro-bravery. Remind her that skill development takes time and practice but she has done it before and she can do it again! Finally, teach her that failure is a good thing; it is an opportunity to try again, to improve, and to grow even more. I can’t tell you how critical it is that we build and boost her confidence—not just today, but every day! In the words of the Dalai Lama, “With realization of one’s own potential and self-confidence in one’s ability, one can build a better world.”  

Lindsay Sealey, MA Ed. is an educator, speaker, consultant, and author of Growing Strong Girls: Practical Tools to Cultivate Connection in the Preteen Years and Rooted, Resilient, and Ready now available on Amazon and Audible. She is the founder and CEO of Bold New Girls and Brave New Boys.

 

 

 

I am a girl advocate and girls champion; the founder of Bold New Girls and Brave New Boys teaching and coaching for girls, boys, and their parents. As well, I am the author Growing Strong Girls and Rooted, Resilient, and Ready (available on Amazon and Audible). I am an international speaker and an instructor with Udemy. 

Christina Aguilera is going back to her Disney roots. Her new music video for the 2020 version of “Reflection” from the new live-action Mulan debuted today. Twenty-two years later, the notes are still big and just as amazing. 

Aguilera performs the newly-recorded “Reflection” in the music video directed by “Mulan feature director Niki Caro (The Zookeeper’s Wife, McFarland, USA).

Starting Sept. 4, with Premier Access, you can watch Mulan before it’s available to all Disney+ subscribers. Disney+ will offer Premier Access to “Mulan” for $29.99 on disneyplus.com. Once you have Premier Access to Mulan, you can watch as many times as you want on any platform where Disney+ is available. 

“Reflection (2020)” is produced by Mulan composer Harry Gregson-Williams.  The original 1998 classic was written by David Zippel and Matthew Wilder. 

Music from Reflection and the new original song Loyal Brave True are featured in Gregson-Williams’ underscore with Aguilera’s full-length versions appearing in the film’s custom main-on-end title design.  Both songs are featured in the movie and on the Walt Disney Records soundtrack, with score composed and conducted by Gregson-Williams. 

—Jennifer Swartvagher

Featured photo: Disney+

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If your kids love Mira, Royal Detective then we have great news for you. Inspired by the hit show, a new short-form series Dance with Mira and Friends is coming to Disney Junior. The new show features Mira and her mongoose friends, Mikku and Chikku alongside real-life kids demonstrating simple dance moves from the series so your little ones can follow along at home. 

Check out this exclusive first look at Dance with Mira and Friends.

Dance with Mira and Friends premieres Mon. Aug. 24 at 8:55 a.m. ET/PT on Disney Channel and will also be available on Disney Junior, DisneyNOW and Disney Junior YouTube.

Acclaimed Bollywood choreographer Nakul Dev Mahajan is the dance consultant and choreographer on Mira, Royal Detective and worked on the new short-form series, breaking the dances down into simple movements.

Dance with Mira and Friends
 Inspired by the cultures and customs of India, “Mira, Royal Detective” is set in the fictional land of Jalpur and follows the smart, brave and resourceful Mira, a commoner who is appointed to the role of royal detective by the Queen. 

Created for kids age 2-7 and their families, each episode features two 11-minute stories which showcase Mira utilizing critical thinking and deductive reasoning to help solve cases for her family, friends and extended community.

The series features an all-star cast of prominent South Asian actors including: Freida Pinto (Slumdog Millionaire) as Queen Shanti; Jameela Jamil (The Good Place) as Mira’s Auntie Pushpa; Kal Penn (Sunnyside) and Utkarsh Ambudkar (Brittany Runs a Marathon) as mongooses Mikku and Chikku, respectively; Hannah Simone (New Girl) as Pinky, a young girl in Jalpur; and Aasif Mandvi (Evil) as Mira’s father, Sahil. Newcomer Leela Ladnier stars as the voice of Mira.

—Jennifer Swartvagher

Featured photo: Disney Junior

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We are anxiously awaiting the premiere of the new live-action Mulan. Disney+ just released the music video for the original song “Loyal Brave True” performed by Christina Aguliera. This is quite fitting as Aguliera sang the title song, “Reflection” from the original animated film. 

In addition to “Loyal Brave True,” Aguilera will also perform a newly-recorded “Reflection (2020).”  

Both songs will be featured in the film and on the Walt Disney Records soundtrack, with score composed and conducted by Harry Gregson-Williams, set for release on Sept. 4, 2020. You will be able to stream Mulan on Sept. 4 exclusively on Disney+ with Premier Access (Disney+ subscription and additional fee required).

—Jennifer Swartvagher

Featured photo: Disney

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