Wednesday, January 29, 2020

Why 'Just Forget and Move On' Is Dangerous Advice When Discussing Trauma and Disability

1,053 words
8 minute read

Chanel Miller says trauma's like a superpower, in that it can allow us to feel all the feelings of a certain time, at a moment's notice.

This is certainly true for me.

People think babies and toddlers don't remember.

But I do.  

SELF-SOOTHING:

I was two years old.  Just awake from my nap.  A blanket on the window, in lieu of curtains.  My sister, still asleep in her crib across the room.  Because no one had yet come to get me, I occupied myself.

Having spent half my life (at that point) in a hospital, I had learned to self-soothe.  My early coping resembled that of kids who spend their early years in orphanages.  (A hospital, like an orphanage, is an institution.  Neither place is a home.)  

I rocked.  

I hung onto the bars of my crib and I rocked my body back and forth, liking that the action brought me closer to my sister - if only for a second.  I liked the motion.  I liked feeling the smoothness of the top of my crib railing.

I rocked harder and harder and harder.

FALLING:

Suddenly, there was no crib.

I was falling headfirst down, down, down until I crashed onto the floor.  I landed with my head in a bowl.  My entire body was stiff - CP activated - but it went beyond that.  Veered into a toddler freeze-response.  I sobbed not from pain - because none registered - but complete terror.

Someone came and picked me up.  Said, "You're okay," and carried me from the room.  Away from my sister who was now awake and scared, having seen me fall.  

All we both wanted was each other.

COPING:

I was in the living room, settled on a lap because CP means I couldn't sit unsupported yet.  My heart was still pounding.  My body still stiff with fear, deep in a freeze response.

[Image: Me, around age 2, on a brown striped couch]

"Here, Toni.  Play with the ball," someone urges.

I usually love my rubber ball with the orange Care Bear on it.  The smell and the smoothness of it. But right now, I don't want it.  Balls won't help.  Balls are nothing.  I know that the time for crying is all done, because we're in another room.  Because I can hear the big people tell each other:

"Just distract her, she'll forget about it.  If we make a big deal it will be worse."

Except it was already worse.  I had just fallen headfirst out of my crib onto my head.  I was hurt and confused.  Why were they trying to act like if I got to play with a ball everything would be okay?  I was mad, but didn't show it. I played with the ball like they told me, eventually slipping into dissociation to cope.

Giving me a ball to play with just felt so...hugely insufficient.  I felt ignored and insignificant.  Aware that they assumed I didn't understand them, and / or that I would not remember this.  Even though I didn't have the verbal ability to express myself, I understood them perfectly.  And I understood the expectation was for me to move on and not think about it anymore.

I slept in a crib until I was nearly four years old, for safety as much as anything else.  

Now, though, when I was awake, I stayed still, still, still lying down and taking comfort in the crib sides high around me.  I coped in other ways, picking up where my cassette tape of nursery rhymes had left off and letting the well-loved songs play inside my head.  I looked around at the Sesame Street poster on my wall.  My Big Bird lamp.

I stopped rocking, the trauma of that fall trapped inside me.

HELPING:

The notion to urge disabled people (kids, teens and adults) to just move on when something traumatizing happens is deeply harmful.  While it often comes from a well-meaning place, it's also ill-informed.  Because it ignores the fact that, if our parents or caregivers are nondisabled, we come from two different worlds.

While falling, for example, may mean temporary fear and pain for a nondisabled child, for a toddler like I was, it no-doubt nudged the lifetime of situations where I was powerless to stop overwhelming pain. 

Similarly, if a disabled child comes home from school and shares that a classmate has been ableist, telling them to 'just forget about it and move on' is only going to alienate them more.  While this advice is possibly helpful for nondisabled people in certain circumstances, it ignores the fact that experiencing ableism is experiencing abuse.  Most visibly disabled people experience ableism whenever we go out in public.  This constant onslaught is traumatic.

So, what can we do to help each other?

I can only speak for myself, but what I needed in the moments after I fell (and beyond them) was comfort.  I needed to be held and soothed and reassured that it was safe to have feelings and safe to talk about them.  I needed words for what I was feeling.  I needed adults around me to talk to me about how I was feeling (yes, even at two!) so I could figure it out.  

I needed to be in control of when I moved from expressing my feelings to playing and processing what had happened at my own speed.  Kids process though play, and repetition.  Often, disabled kids are discouraged from "dwelling" on difficult things.  This ignores the vital step we might need to take in processing what happened to us.  We need to not be rushed into being okay before we are ready.

We can know that trauma does not always exist in the moment a toddler loudly crashes to an uncarpeted floor from their crib, when they are loudly sobbing.  Sometimes, trauma exists in their stillness.  Their compliance.  Their quiet.

While it's definitely not helpful to see our grown-up loved ones in tons of distress over what happens to us, we need you to be a safe place for us to have our feelings.

So we know that feelings are okay to have.

It won't make us feel sorry for ourselves.

It will arm us, and make us even more able to cope as we grow.

***

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Monday, January 27, 2020

We Belong: Chapter 4

619 words
5 minute read

CAMPING OUT
(Jesse)

Lexie is super lucky.  She gets her own room.  I wouldn’t care if I had to sleep in the smaller room if I just got some peace and quiet.  Seth sleeps like a tornado.  Tossing and turning.  Waking up and crying.  When he finally is asleep, he grinds his teeth.

It’s the weirdest sound I’ve ever heard.  Like aliens talking.  It’s creepy.  It’s awful going from sharing a room with both Lexie and Seth to just Seth now.  I want Lexie back.  Sleeping in the same room as a kid with a race car bed is just annoying.  I want bunk beds again.  It’s weird being so close to the ground.

Scrape-scrape-scraaaape.

I sigh.  Then I think about throwing a pillow at Seth but that would wake him up and make him cry and then I would be in trouble.  Instead, I grab my pillow and sneak to the door, hoping it won’t creak.  

There is no third bedroom right now, so Mom and Dad are sleeping on the bed that folds out of the couch.  I wish I could sleep there.  Let Mom and Dad deal with Seth.  I peek out the door and see Mom and Dad still busy unpacking boxes.

I take a deep breath and two quick steps and I’m in Lexie’s room.

Closing the door behind me softly, I breathe a sigh of relief.

“Miss me?”

I jump and it feels like I’m never going to calm down again.

I can just make out Lexie’s smile in the dark.

“Don’t do that,” I whisper angrily.  I fling my stuffed rabbit, Carrot Breath, at my sister, to retaliate.  Then I toss my pillow.  “Move over,” I say and climb in next to her.

“In the old house when we all three shared a room, you said you couldn’t wait to get out,” Lexie points out.

“Yeah, away from Seth.  He sleeps like a garbage truck.”

Lexie giggles.  “Snoring?  That’s funny…”

“Not snoring, and it’s not funny.  So, I decided, I’m going to camp out with you instead.”

“Yay!  I missed you even if you didn’t miss me.”

“I did,” I admit.  “It’s weird sleeping alone  Now be quiet or Mom and Dad are going to make me go back to Baby Town.”

It’s quiet except for the TV on playing a cooking show in the living room.  I love cooking shows.  I want to be a chef.  Our dad’s a chef, kind of.  He makes all our food.

“Jess?”

“What?”

“I don’t want to have surgery.”

“I know.  But let’s not talk about it, okay?”

“Yeah.  Hey, you brought Carrot Breath,” she smiles and pulls Mr. Hopps away from the spot by the wall.

[Image is: One tan rabbit and one brown rabbit sharing a carrot]

Carrot Breath and Mr. Hopps catch up about where the best spots in the yard are to find carrots.  Carrot Breath is so hungry he decides to go to the refrigerator if he is hungry.  Mr. Hopps wants to go, too, and check for radishes and that’s disgusting.

We stop playing.

“We’ll always be together, right?” Lexie asks.

“Yeah, of course.”

“Good,” Lexie yawns.  “Don’t kick me tonight.”

“Don’t steal the blankets and I won’t have to…” I retort.  Then I turn over and try to get comfortable.  With Lexie close, I fall asleep in no time.




Questions for Discussion:

Jesse thinks Lexie is lucky she gets her own room.  Do you prefer to have your own room, or share with someone else?

Jesse and Lexie play pretend with their stuffed rabbits.  What do you pretend when you play?


***

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Saturday, January 25, 2020

Books I've Read in 2020: 1-5

985 words
8 minute read

1.

Genre: Historical Fiction

Disability Representation: Yes (burns and trauma)

Rating: 4/4 Wheels (Loved it!)

Excerpt of GoodReads Summary:  Why is the land so important to Cassie's family? It takes the events of one turbulent year—the year of the night riders and the burnings, the year a white girl humiliates Cassie in public simply because she's black—to show Cassie that having a place of their own is the Logan family's lifeblood. It is the land that gives the Logans their courage and pride—no matter how others may degrade them, the Logans possess something no one can take away.

What I Thought:  I've heard excerpts of this book read aloud to me as a teenager, and I'm pretty sure I read it in my 20s as well...but I feel like this time...it hit me right in the gut.  Holy God.  I can so see why this one's an award-winning book.  As a child, certain aspects of this story stood out to me, but now...  It's like...fully seeing what both the children and the adults in the Logan family had to contend with...  It's mind-blowing.  Such an amazing, heartbreaking story.

2.

Genre: Young Adult

Disability Representation: Yes (Schizophrenia mainly, I think.)

Rating: 2/4 Wheels (Liked it)

Excerpt of GoodReads Summary:  Caden Bosch is a brilliant high school student whose friends are starting to notice his odd behaviour.

What I Thought:  I tried to read this book a few years ago, and got maybe over halfway through before abandoning it.  It is admittedly hard to follow, going back and forth between Caden's real life and his inner life / thought life.  Based on what I saw via reviews on GoodReads from people who shared aspects of Caden's diagnoses, they say the representation in the book is stunningly accurate.  (And it has to be mentioned that author, Neal Schusterman collaborated on this book with his son, Brendan Schusterman, who shares Caden's mental health conditions) and it shows.  It was amazing to read such neurodiverse representation.  Had it been easier to follow, I would have definitely rated it even higher.

3.

Genre: Musicals

Disability Representation: Yes (social anxiety, various other mental health things)

Rating: 2/4 Wheels (Liked it)

Excerpt of GoodReads Summary:  A letter that was never meant to be seen, a lie that was never meant to be told, a life he never dreamed he could have. Evan Hansen is about to get the one thing he's always wanted: a chance to finally fit in. Both deeply personal and profoundly contemporary, DEAR EVAN HANSEN is a new American musical about life and the way we live it.

What I Thought:  To be honest, we've had this book for a while, but it's taken me a while to read it.  Jordan Fisher joining the cast as "the first ethnic Evan" (from January to May, 2020) is a big motivator.  Knowing I won't get to Broadway to see this, I endeavored to absorb all the Evan Hansen I could in every possible way.  So, I did like the book.  Tara and I cried several times.  The musical is incredible and it was great learning about the actors and writers.  But as usual, tracking issues made actual reading difficult for me.  This book has large pages and columns that were hard for me to follow.  (Hence the two wheels.)  But it was a good one, and I'm glad to have read it.

4.

Genre: Psychology

Disability Representation: Yes (trauma)

Rating: 3/4 Wheels (Really liked it!)

Excerpt of GoodReads Summary:  What happens when a young brain is traumatized? How does terror, abuse, or disaster affect a child's mind--and how can that mind recover? Child psychiatrist Bruce Perry has helped children faced with unimaginable horror: genocide survivors, murder witnesses, kidnapped teenagers, and victims of family violence. In The Boy Who Was Raised as a Dog, he tells their stories of trauma and transformation through the lens of science, revealing the brain's astonishing capacity for healing.

What I Thought:  This book was super eye-opening as far as information about how early neglect and trauma can impact a young brain.  I really loved reading most of the case studies and getting to know the different children and what was done to help them.  I also appreciated reading the most up-to-date version (though there were a few unevolved disability attitudes which is why I couldn't give it 4 wheels...)

5.

Genre: Childrens > Middle Grade

Disability Representation: Yes, (mental health) also D/deaf representation.

Rating: 2/4 Wheels (Liked it)

Excerpt of GoodReads Summary:  After all the backstage ghost drama during Phantasm, things are quiet for the Backstagers of the St. Genesius School Drama Club. Too quiet. But when that quiet is filled by a mysterious voice that haunts the Backstagers day and night, they set off on a globetrotting adventure to discover the ancient secrets of the legendary artifacts of the theater. Can they solve the mystery in time to open their production of the rock musical Tammy?

What I Thought:  This book was dedicated to the cast of Deaf West's Spring Awakening, and written by Andy Mientus.  Because of this, I was eager to read the D/deaf representation, especially.  Knowing that Mientus did have input from a couple of DWSA castmates on the D/deaf character did show, as the representation was stronger than I'm used to.  Still Adrienne read a bit like token representation.  She's very much on the outside of the group and she didn't have much say over what happened to her.  I did like reading how the characters adapted for her, showing that it is possible to include others in theatre productions.  (An especially good message for kids!)  The mental health representation, on the other hand, did feel quite authentic and that character was quite layered.  A good read.

Related:  37 Books I Read in 2019 / 30 Books I Read in 2018

***

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Monday, January 20, 2020

We Belong: Chapter 3

468 words
4 minute read

TERRIBLE THINGS
(Lexie)

I’m pretty sure Jesse jinxed us.

Later that night, after supper and watching a movie on our I-Pad, Mom, Dad and Jesse come into my room.  My bed is moved in, and my clothes, but not much else.  It’s probably the only time ever my room will be this clean.  Maybe I should take a picture of it.  I’m okay with it being small, if it’s just me that lives in it.

“Jess, Lex,” Mom says, sitting down next to me on my bed.  Dad and Jesse are on it, too.  I think for one second what if we break it?  Then I might have to sleep in the boys’ room.  That would be terrible!

“What?” Jesse asks warily.

“You’re not in trouble,” she smiles.  “But your dad and I need to tell you something.  Do you remember the last time we went to Children’s?”

We nod.  Children’s is Children’s Hospital where Jesse and I have to go sometimes so that doctors can do lots of tests on us to see how our CP is.  They stick stuff on us and watch us walk.  It doesn’t hurt but it takes forever, and we don’t like it much.  Sometimes we need to get braces made for our legs.  Luckily that didn’t happen last time.

“Well, you guys are going to be having surgery.”

Jesse and I look at each other.  “When?” we ask together.  That happens when you’re twins sometimes.

“In a couple of weeks.  On June 25th.”

I look over at my calendar of funny cats.  Today is June 11th. June 25th is exactly 14 days away!

[Image: Cartoon cats teach each other math]

I grab my favorite stuffed animal, a rabbit named Mr. Hopps, and cuddle him to my chest.  I’ve had him ever since I was four and had my first surgery I can remember.  I had other surgeries, too, when I was five and seven.  I was hoping to never need another one.  But Mr. Hopps comes with me every time and makes me brave.

Jesse takes my hand.  “Both of us?”

Jesse has only had one surgery when he was three.  He doesn’t remember anything except the scary noise the machine made taking off his cast when his leg was all better.

I see Mom and Dad nod yes to Jesse's question.

We are both having surgery at the same time.

I swallow and try to hear everything Mom says, but all I can think is: my whole summer is ruined.





Questions for Discussion:

Were you ever told you had to have surgery like Lexie and Jesse?  How did you feel?

Would you rather have surgery along with someone else?  Why or why not?

***

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Monday, January 13, 2020

We Belong: Chapter 2

722 words
6 minute read

CP AND ME
(Lexie)

You know some things about me, but you don’t know everything.  Here is a list of things I tell people about myself:

1.  My name is Lexie Martin.

2.  I’m a twin.

3.  I’m nine years old.

4.  I have CP.  I like saying CP more than Cerebral Palsy because it’s shorter and sounds less scary.  Also, I only tell people about my CP if I want to.  When mean kids are rude, I don't want to talk to them about it and I don't have to.

Cerebral Palsy means something happened to my brother and me when we were being born because we came too early.  That means our brains sometimes get confused when we try to move our bodies.

Even though we're twins, Jesse has different CP than me.

Jesse has CP because brain got a little bit hurt on the inside.  He walks with a limp and on his right side the muscles are tighter and confused, but not very much.  He can do almost everything, and nobody knows he has CP unless he tells them.  Sometimes I feel jealous of that.

Everybody can tell that I have CP.  I was born second, so I had to wait longer to breathe air than Jesse did.  People's brains need oxygen to do all the things brains do.  If a baby's brain doesn't have enough air to breathe, that's another reason they can have CP.

In my body, the muscles in both my legs are tight and confused, sometimes, in my right hand, too.  The only part of my arms and legs that escaped CP was my left hand.  Its muscles are totally fine.  (Thank goodness, because I’m left-handed.  So is Jesse.)

This probably sounds like a lot, but for us, it's really normal, I promise.  The worst part is people around us making us feel bad for having CP.  Like those kids who rode by on bikes and scooters.

I walk with a walker (outside) and crutches (inside, and on stairs).  At school, I will also use my walker.  On trips with lots of walking, I take my wheelchair.  My wheelchair is the best.  It’s yellow and black.  Dad calls it the Batmobile.  That’s a car Batman drove or something.  It’s speedy fast.  My walker doesn’t have a name.  My crutches don’t either.

I wish I didn’t need anything to walk like Jesse.  Kids don’t make fun of him that much.

“Hey Lexie Lou,” Dad says.  (All of us kids have the middle name Rowan.  It was mom’s last name before she got married to dad.)  Usually, I laugh at that corny joke, but not today.  Not right now.

“That’s not my name,” I say, but my heart’s not in it.  I sigh and sit down next to where he is washing dishes. “Some kids asked what’s wrong with me.”

“Oh,” Dad nods, with a not-pleased look on his face.  “Did you ask what’s wrong with them?” he asks with a little smile.

“Rudeness, I already knew that,” I smile a little.  Dad always makes me smile.  “But, Dad, I can never think of the words in time.  It’s like everything gets stuck inside me.”

“Well, let’s think about this,” he says.  He picks me up and sets me on the counter so I can see his eyes.  He holds on, so I don’t lose my balance.  “What did you want to say to those kids?”

“Nothing,” I say right away.

He squints.

“Because nothing is wrong with me.  Having CP isn't wrong," I say.

Image: A brown cartoon sign reads What If Nothing is Wrong?


“That’s right,” Dad says, and I can tell that he definitely believes it's true.

It doesn't change everything.  (Dad still doesn't know what it's like to have CP.)  But it helps a little bit that he doesn't think what those kids think.




Questions for Discussion:

Lexie's dad calls her wheelchair the Batmobile.  Have you named any of the things that help you? If so, what?

Lexie's dad made her feel better by letting her know he did not agree with the kids who were mean to her.  What's the best way people can make you feel better when someone is mean to you?


***

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Monday, January 6, 2020

We Belong: Chapter 1

730 words
6 minute read

MAPLE STREET
(Lexie)

TW: Ableism

“Jesse!  Stop it!  This is my room!”  I say, standing in the doorway, so he can’t keep trying to get in.  “Mom already said.  You and Seth have to share.”  We just moved into 2424 Maple Street.  It’s a nice house.  The best part is, I get to have my own room.

Jesse is my twin brother.  We’re nine years old.  Usually he’s super nice, but today he’s being a pain.  Seth is our little brother.  He’s only three and an even bigger pain.  I think it’s a great idea to put the two of them together.

With no furniture in the house, it looks gigantic.  The other best part is the basement, which is the biggest room I’ve ever seen.  Dad says we can only go down there when grown ups are down there, too.  But I already have plans to send Jesse down to spy around and see what is so amazing that we can’t see it.  When I looked, it was just a concrete floor and bare walls.

“Lexie!  My room!” Seth demands.

“No, your room is over there,” I point to the one next door to mine.  It’s smaller.

Seth’s bottom lip sticks out.  “Daddy!  That’s my room, right?” he pouts.

“That’s right, little buddy,” Dad says happily, swinging Seth up on his shoulders.  I feel jealous.  Seth gets everything.

“That’s not fair!  I claimed this one!” I protest.

“You’re getting your own room.  Your brothers have to share, so it makes sense that they have the bigger room.” Mom says, carrying in a big box and setting it in the hall.

“No it doesn’t.  That makes zero sense,” I complain.

“Why don’t you kids go out and play?” Mom suggests.  She’s trying to make me forget about having the smaller room, but I won’t.

“...Maybe because the yard’s full of dirt?” Jesse mumbles.  He’s such a crab today.

“Aha!  I knew it was in here somewhere!”

“What is that?” I asked, looking at the weird plastic bucket Mom’s holding.

“Sidewalk chalk,” she announces, like it’s money.

“Me!  I want that side-bawk-bawk!” Seth screams, like there’s a chicken in the bucket.

“Fine,” I huff.  “Come on, guys.”

Outside, we sit on the front steps and Seth dumps every piece of chalk out.

[Image is: Lots of multicolored sidewalk chalk dumped out]

“What’s your problem?” I ask Jesse, bumping him with my shoulder.

“Um, hello?  We moved!  Terrible things happen to kids who move!”

I laugh.  “What terrible things?”

“No grass in your yard, no furniture in your house, you have to share a room with a baby…”

“Hey!” Seth said, waving a yellow chalk at us like a weapon.  “I can color on you…”

“Plus, we moved away from Connor and Shane.  Now who am I supposed to hang out with?”

“Hello?  Me!”

“I know!  But other than you…  Doesn’t it bug you we moved away from all our friends?”

“Not really…” I admit.  Jesse is forgetting that I don’t have many friends, other than him.  Those two boys he named?  They’re our cousins.

Just then, a kid rides towards us on a scooter, and two more on bikes.  They stop right in front of our house and stare at me.

“What’s wrong with you?” one demands, taking off her helmet to stare at me even more.

I bite my lip.  My ears feel hot, and I can’t say anything.  I feel Jesse move closer to me.

“Hey guys!  Wanna color with us?” Seth asks, waving them over.  He’s too little to know how mean they are.

“Say we have to go inside,” Jesse whispers.

“Mom says we have to go inside,” I repeat it louder.

The kids all laugh.  “Oh my gosh.  They’re such babies!  Let’s go, guys!”

I shove my walker back away from me.  I push my crutches so they fall down.  Sometimes, I hate them and all the ways they make me different.

Right then, I know Jesse is right.  Terrible things do happen to kids who move.





Questions for Discussion:

Have you ever felt like Lexie and hated the way disability made you different?

Jesse whispers that Lexie should say they have to go inside when kids are mean to them.  How do you respond when kids are mean to you?

***

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Friday, January 3, 2020

Finding Joy and Purpose While Disabled

337 words
3 minute read

It's taken most of my life to wrap my head around the reality that my worth does not lie in my productivity.  Often, through the years, I've been bombarded with ableist messages coming from everywhere I look:

"You never DO anything!"

"Aren't you going anywhere on vacation?  Just staying home isn't fun!"

"There's more to life than the four walls of your apartment!"

The key, for me, was found in cutting ties with toxic people and instead surrounding myself with those who were "safe enough."

Nondisabled society especially, embraces the belief that in order to live a worthy life - a purposeful life - a life with joy?  We must be constantly in motion.

Disabled culture, in many ways, is different:

There is so much joy in rest!  In surrounding yourself with whatever safe things and people you can!  Joy and purpose can be found in our hobbies, in our time with loved ones, in watching a favorite show or listening to music we love.

May we resist nondisabled logic that tells us we can't have joy or purpose because our lives look different from theirs.

We make our own joy in this life.

So start small.

What makes you smile?  Revel in these things!  (If you haven't found your thing yet, browse Netflix, chat online with disabled friends, cuddle your stuffed animals, smell a candle.)  You can start anywhere to cultivate joy.

You are here for a purpose.  Whenever you intentionally decide to prioritize your safety, listen to a friend, help someone else, share your joy, or a hobby you love?  That all matters.

Our worth does not lie in what we can do.  It lies in who we are.

Surround yourself with people who love you for you.  (Trust me, we're out there.)  And you will be okay.

On Christmas morning, I got a stuffed Stitch...and I was super happy about it.

Sound off in the comments disabled friends:

What gives you joy?

What's your purpose?

***

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Thursday, January 2, 2020

We Belong (a middle grade novel)

318 words
2 minute read

[Image: A book cover reads We Belong by: Tonia M. Christle.  A purple-hued tree with electric roots.  The silhouettes of a boy and a girl can be seen]



Author's Note:

We Belong is the story of twins, Jesse and Lexie, and their lives together growing up with CP.

I began writing this middle grade novel in the spring of 2016 and continued into the summer of that year.  On January 1, 2020, I found my notes for it, and ended up finishing the book, adding the final four chapters.

Though not published in the traditional sense, you'll find the full table of contents here - with links to take you to each chapter.  

- Tonia M. Christle
January, 2020
--


Dedication:

For Nina,
So you will know we are not the only ones.


CHAPTER 1:  Maple Street 

CHAPTER 2:  CP and Me

CHAPTER 3:  Terrible Things 

CHAPTER 4:  Camping Out 

CHAPTER 5:  Sometimes, I Can't 

CHAPTER 6:  Grandma and Grandpa's 

CHAPTER 7:  Special Things 

CHAPTER 8: Playing at the Park 

CHAPTER 9: The Night Before 

CHAPTER 10: Gross O'Clock 

CHAPTER 11:  Time To Go 

CHAPTER 12:  Waking Up 

CHAPTER 13: Hospitals Are Boring 

CHAPTER 14:  Nothing To Fix

CHAPTER 15: Therapy or Playing? 

CHAPTER 16: So Many Changes

CHAPTER 17: How It Feels

CHAPTER 18:  Going Home

CHAPTER 19: Together Again

CHAPTER 20: Snail Mail

CHAPTER 21: The Secret Club

CHAPTER 22: Fitting In

CHAPTER 23: Super Sonic Hearing

CHAPTER 24: Doughnuts and Disappointment

CHAPTER 25:  Just Like Me

CHAPTER 26: Baking and a Big Oops

CHAPTER 27: A Fair Trade?

CHAPTER 28:  Sophia The Worst

CHAPTER 29: Telling Mom

CHAPTER 30: Missing

CHAPTER 31:  The Plan

CHAPTER 32: Candy Rescue

CHAPTER 33:  Mission Accomplished

CHAPTER 34:  Something's Wrong

CHAPTER 35:  Left Out

CHAPTER 36:  About Belonging

CHAPTER 37:  Do You Love Us?

CHAPTER 38:  Not Embarrassed

CHAPTER 39: Surprise!

***

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