Monthly Archives: October 2016

Meet Hazel

 

hazelMiss Hazel is here to celebrate day 23 of Down Syndrome Awareness Month with us! I introduced to you Hazel last October and am so happy to have her back as a four-and-a-half year-old this year. You can find Hazel and her family on her mama’s blog ChasingHazel.com and on Instagram @chasinghazel.   Thank you, Steph, for taking the time to share your gorgeous girl with us!

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What would Hazel do if she could design her very own day?

If Hazel could design her own day, she would get up bright and early and jump right into her daddy’s arms. He’s her all time fav. (I believe the feeling is mutual.) If she could shrink him and stick him in her pocket THAT would definitely be ideal. If not her dad, her Nonna is next in line.

She might choose to go to school, hang on the monkey bars with her friends and sing together with them at circle time. Likely, she would carve out some time to play with her shadow and/or look at herself in the mirror. That’s where she practices all her songs and the signs she’s learned. She has some pretty lengthy conversations with herself in that mirror.  Then, if she could find time in the day, we would certainly be at the park where she loves to climb all over everything and go down the slide. Or, maybe she would rather go for a long walk outside with her sister. THE BEACH!!! She LOVES the beach. Splashing in the waves, swimming and jumping into the water all bring a huge smile to her face.

Heading into the evening, Hazel would ask me to listen to all her favourite songs or watch a movie while eating a bowl of Sunchips. Her current favourite songs are, “A Woman’s World” by Cher, “My Church” by Maren Morris, the theme song for Tinkerbell, and any Jimmy Fallon Lip Sync Battle. Once her chips were done she would ask to listen to all the songs again so she could dance this time around. Think…”If You Give A Mouse a Cookie” but “If You Give Hazel A Song…” Her top movies at the moment are Shrek, Tinkerbell, Frozen and Peanuts.

Oh, and if she could just eat pasta, pizza, chips, grapes, ice cream and Oreos that would be fantastic. All of which are free range, organic so it’s cool. #nope

 

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What has Hazel taught her sister, Nola? What has her Nola taught Hazel?

Since Hazel came first in birth order I really didn’t spend much time stressing about what having a child with special needs would mean for a sibling. When I found out I was having another little girl though, my heart nearly exploded right out of my chest. I felt that we were given the most perfect person to care for, nurture, shape, love and teach Hazel for a lifetime ahead. What I didn’t realize at the time was how Hazel would nurture, shape, care for and teach her younger sister, Nola.

There could not be a more perfect pair. They are extreme opposites in every single way except for the fierce love they have for each other. They laugh, play, run, jump on the bed, fight, cry, yell (well mostly Nola yells…sigh), hit each other (well mostly Nola hits…double sigh). They do all the things that siblings do. Good and bad. They look for each other when they aren’t together, walking all around calling out each others names, “NOLA?? Where are you??? NOLA???” and vice versa. They sit together, criss-cross facing each other and talk in a language that only know AND they think it’s hilarious! They sing and dance together. They share with each other.

They are learning to be partners. They are learning to be friends. They are learning to be sisters.

 

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What is the most wonderful part of knowing her?

The most wonderful part of knowing Hazel is the way that she has helped me to really FEEL. Until I laid eyes on her, I had no idea what unconditional love meant. She taught me right from the beginning how to love in the biggest, most wholesome way. And not only for her, for everything. The world was a big new place that I hadn’t seen before in this way. Like my heart had not really been beating at all before she came along. My vision once blurry became crystal clear. Everything heightened.

When I feel pride for her it nearly knocks me down in my tracks. When I feel discouraged it almost cripples me. When I see that bright, smiling face of hers, my heart skips a beat. When she brings me in for a hug or a kiss, well – I almost melt into a puddle right there on the floor. It’s true love – a fairytale.

The real beauty is watching her interact with every. Single. Other. Person. Her purity and sparkle surpass all borders. Even the most reluctant of people in the grocery store are taken by her. All she has to do is flash them her smile, and a “HI!!!! How are YA?!!!” They are hers. I watch everything wash away and see them truly FEEL happiness even if only for a moment. Every room we walk into is brighter not only because of her smile but because all the other people are smiling back at her. You can almost feel their hearts beating a little faster when she’s around.

Being able to witness the joy your daughter brings to the world has been one of the greatest gifts that she has given me. I feel honoured to walk beside her. She is absolutely perfect in every single way. I can not imagine how I would have gone through life feeling as blessed and fulfilled as I do right at this moment without my sweet Hazel.

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Check back tomorrow as we continue celebrating Down Syndrome Awareness Month or click below to read all of our previous posts.

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Meet Charlie

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Do you remember this handsome fella from our month of celebrating last year? He was itty bitty than, but Charlie is now a strapping 19 months old and has clearly just become more adorable every day in the last year. Alissa, with your girls included, how on earth do you handle all the cuteness in your house? Friends, Alissa and her Charlie are joining us to celebrate day 22 of Down Syndrome Awareness Month today! You can follow them on Instagram at @deerpathponderings.

 

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What has Charlie taught his siblings?  What have they taught him?
In the short time Charlie has been in our family he has taught us many things.  Charlie has taught his older sisters that people with Down syndrome can do anything.  I just love how my daughters aren’t aware of the misconceptions that people have about those with Down syndrome.  They often wonder what Charlie’s job will be when he’s older and how many kids he will have.  It’s encouraging to me to see that they don’t put limits on him and I shouldn’t either!  Charlie has taught his older sisters the joy of having a little brother.  Someone who loves cars, eating grass, and getting dirty.  I am confident that they will become better people for having Charlie as their little brother.  Charlie’s older sisters have taught him how to say “more”, climb the stairs, and be a part of our family.  They love reading to him, playing violin for him, and helping him walk.

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What are a few things that they are really good at?
Charlie is a good eater!  He has been my least picky kid when it comes to food.  He has also learned the sign for “more” lately and uses it often.  So far, he thinks it only applies to food!  Charlie is good at climbing the stairs.  Lately, he climbs them so stealthily that I don’t even know it til he makes it to the top.  Charlie is great at pushing his toy cart.  He’s getting more confidence and strength to help him to walk.  He’s already great at the bear crawl and very fast at it too!

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What is the most wonderful part of knowing Charlie?  I just love how Charlie makes people smile.  He is so full of joy that it rubs off on the people he meets.  Another wonderful part of knowing Charlie is the fact that God gave him to us for a reason.  It’s exciting to think about how God will use him to impact the world, including us, his family!

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Check back tomorrow as we continue celebrating Down Syndrome Awareness Month or click below to read all of our previous posts.

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Photo Friday

 

Photo Friday is a little glimpse at our week in pictures. To see more, follow @TheMangoMemoirs on Instagram!

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Meet Stella

 

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Say hello to Stella! This little miss is three years old and is another one of our family’s Instagram loves. You can find her there under @stellamagic. Today her mom, Andrea, answers a few questions about her darling girl for day 21 of Down Syndrome Awareness Month. You can find Andrea on Instagram at @arod4481. Thank you for sharing with us today, Andrea and Stella!

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What are some things Stella likes doing?
Playing outside. Watching TV. Dancing to music videos and playing in any kind of water!

What are her favorite and least favorite foods?
She hates milk and water, but she loves smoothies, apples off our tree and goldfish crackers.

What are her favorite movies and books?
Pete the Cat, Sesame Street and Wallykazam

Who are her favorite cartoon characters?
Wallykazam and Elmo

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What would Stella do if she could design her own day?
She would have the sliding glass door open and go back and forth between outside and the couch watching TV while eating goldfish crackers. And she would be swimming in a pool we don’t currently have.

What are a few things she’s good at?
She is really good in the water for not having access to a pool. And she is good at playing kickball.

What is something you want everyone to know about your daughter?
Her smile and giggle can light up a room. She does anything she wants to do, and she is not limited to anything.

Finally, what is something you don’t think many people know about Down syndrome?
People don’t have to feel sorry for parents of children with Down syndrome. We don’t feel sorry for ourselves!!

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Check back tomorrow as we continue celebrating Down Syndrome Awareness Month or click below to read all of our previous posts.

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Meet Leo

 

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Meet two-year-old Leo! This handsome guy is here today to help us celebrate day 20 of Down Syndrome Awareness Month. You can find his mama, Hillary on Instagram and Twitter as @hillaryschu and his dad, Michael, on Instagram as @goodbeerhunting and Twitter as @mpkiser.

 

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What are some things Leo thoroughly enjoy doing?
Leo loves to watch tv, play apps on the phone, and read books. He loves to run around the park, kick balls, and chase people. He likes to dance and play jokes on people. He loves to blow kisses and give high fives.

What are his favorite movies, games, or books?
Leo loves books—his favorites change often. He’s currently really into “The Book With No Pictures,” “Along a Long Road,” and “Pigeon Wants a Puppy.” His favorite TV shows are Curious George and Sarah and Duck (and he likes Mother Goose Club on YouTube). Leo likes pretty much all games. Right now we are playing My Very First Games – First Orchard and Thinkfun’s Roll and Play Board Game—games where he has to take turns and follow simple directions. He has a pretty long attention span for a toddler.

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What are a few things Leo is really good at?
Leo is great at matching and puzzles. He’s a good mimic and we’re working on his ABCs (he knows them just can’t quite say them all yet). He can identify colors, name all of his family members, and feed himself. He’s done a little modeling and he’s really good at it. He follows direction really well. He also does the best frog impression that you’ve ever heard.

What is the most wonderful part of knowing them?
Everyone loves Leo—joy just pours out of him. From the minute he was born, people have been drawn to him. Strangers smile at him, the girls at the grocery store fawn over him, everywhere we go, someone stops to talk to him. It has always felt like he was important—bound for something great—and I love just being near him, let alone helping to shape the man he’ll become.

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What is something you don’t think many people know about Down syndrome?
When I first found out in utero that Leo had Down syndrome, I was worried that he wouldn’t look like me or my husband. That he would look like “Down syndrome”—whatever I thought that was. But Leo looks JUST LIKE ME. Looking at photos of other parents and their kiddos with Ds, you can always see the resemblance.

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Check back tomorrow as we continue celebrating Down Syndrome Awareness Month or click below to read all of our previous posts.

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Meet Macyn & August

 

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I am thrilled to have Macyn & August with us today as we celebrate day 18 of Down Syndrome Awareness Month! I have been following this sweet family for the last few years and am consistently inspired by mama Heather’s posts. I remember the joy they shared when Truly (their middle child) and August joined their family through adoption and the hashtag #theluckyfew came about.  (Seriously, check out the hashtag. It’s amazing.) And the super exciting thing is that Heather is set to release a book about their journey in March 2017! Click over to her website to check out The Lucky Few book and to read her blog. You can also follow this crew on Instagram at @macymakesmyday. Thank you, Heather, for celebrating with us today!

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Do your kids have a favorite cartoon or movie character?
All the kids are crazy about Disney everything right now. We have annual passes to Disneyland and all they want to do is go to the shows to see the characters and walk around looking for the characters. August is especially obsessed with Goofy, which Macy loves them all.

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Who do they love to spend time with?
Macy loves to spend time with almost anyone of her family or friends. She LOVES being with people, it gives her life. She is always inviting people over to hang out and everyday asks who we are going to see. Macy especially loves her grandparents, aunties, uncles and cousins. Her cousin Kalli, who is closest to her in age, is her very favorite person to be with.

August, on the other hand, just wants to spend time with his dad and me, and his sisters too!!!! He gets shy and reserved and even nervous around anyone else. In his ideal world, we would be touching at all times, or at least always in the same room!

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How are they similar to and different from one another?
Macy and August both have Down syndrome, yet they could not be more different. Macy is our little miss cautious. This makes her less willing to try anything new. She is huge on expectations and when she does not know what to expect, or her expectations are not met, she gets bummed out and can tend to shut down (I’m the same way!). August is mr. throw caution to the wind. He is daring and bold and willing to try everything (except food!). He is also very high drama (can you say “drama king”?) while Macy is calm, and even when things feel stressful or don’t go her way, she never responds with dramatic outbursts. Because they both have Down syndrome we see some similarities in development etc., but really, they could not be more different.

Then there is our middle daughter, Truly, who does not have Down syndrome or any other kind of different ability. Truly is a born leader and is pretty sure the only way to do everything in life is her way. Sometimes her siblings put up with it and let her lead the room, sometimes there is plenty of bickering as Macy and/or August get frustrated with her inability to allow them to be in charge:). Truly is highly emotional and loves to take risks, just like August.

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What is the most wonderful part of knowing your children?
Knowing my kids with Down syndrome is like having a front row seat to a kind of magic. They have shown me that when we take the ups and the downs, the good and the bad, the celebrations and the sorrows, the bravery and the fear, and we intermingle them until we can hardly tell them apart, what we get is a new kind of beauty, a new kind of reality, that I have not found to exist anywhere else.

What have you found to be good resources for learning more about Down syndrome?
The best resources are people who have Down syndrome or have a loved one with Down syndrome. Find us on social media, ask questions, let us become a part of your normal day to day lives. There is no better resource out there.

 

Check back tomorrow as we continue celebrating Down Syndrome Awareness Month or click below to read all of our previous posts.

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