“Pain and Torture” The Value of Physical Therapy

Therapy

Eating lunch at home with my left hand. A Special Thanks to Traci Gee and Sarah March for helping me get ready to hold my nephew. Those three weeks together were sure an adventure!

Pool

Getting ready to swim at the YMCA

Traci

In the Water with Traci Gee July 2013.  Swimming is one of my favorite Summertime Activities! I’m a Mermaid in the water!

caden and Aunt Ra

Here’s the reason I learned to use my left hand. In this picture, he’s about four months old. (I think) Now he’ll be three in January  They grow up so fast!  By the way, his middle name Rex is in honor of my dad who passed away in January 1995. Too bad Dad isn’t here to meet his grandson.

Jensen Family

The Jensen Family 2015. On the left is my sister Roz Jensen. Next to her is her husband, Cody Jensen. My sister is holding Brynn who was born August 3rd 2015. We just celebrated her first birthday. I’ll have to write a story about her next. If Caden sees my mom without me, the first thing he says is, “Where’s Aunt Rachael?” He can’t wait to see me! I love him too! We always have a great time together! What a great family!

I have cerebral palsy. Over the years I’ve had lots of physical therapy throughout my life. Physical therapy helps me strengthen my leg muscles which helps me be able to do things like transfer to a car; get in and out of bed, etc. Sometimes when the physical therapist is stretching my legs and holding it up on their shoulder it can be painful if the muscles haven’t been stretched out enough. Sometimes, as my mom is watching me and she sees the look on my face, she says,

This is liable to look like pain and torture you know that?” The therapist smiles and we laugh.

As a child, I didn’t like going to physical therapy. Now that I’m an adult, I’ve come to appreciate the benefits of physical therapy.I especially appreciated it in the summer of 2013 when I knew my new nephew would be arriving soon. I’m a children’s author and I really love children. I couldn’t wait to hold my newborn nephew  First I had to get my left hand working better I used my right for everything my left hand just sat there. It wasn’t that I couldn’t use my left hand but my left hand is slower at doing things so I get impatient and let the right hand do it all. Holding a baby takes two hands. I can use my left hand, but my right hand is more relaxed because I use it more.
In order to get my left working well enough to hold a baby, I did all kinds of things. My friend Sarah came in and helped me. During the summer of 2013, Sarah helped me train a new caregiver named Traci who would take care of me during the week. For three weeks, Sarah Traci, and I did lots of physical therapy. At lunchtime, they put my right arm in a sling so that I had to use my left arm for everything. Picking up the drink, picking up my sandwich etc. Trust me there were many times I thought, This is crazy. My tea is in a huge aluminum container. When It’s full, it’s really heavy! Many times as I tipped it up to take a drink I’d spill tea down the front of my shirt or even drop the container on the floor. What a mess! When something is not habit repetition is the key. That’s true for anyone but especially someone like me who struggles with getting the right messages to communicate with the right parts of the body so I can do the small everyday tasks.
At times I sighed and wondered, Why am I doing this again? Then I’d tell myself silently, Baby, Baby, Baby. That got me motivated again. I continued working to strengthen my left hand. When I was at the computer at home, Traci would switch the mouse pad over to the left side. I moved a few icons around on the desktop. At the hospital, it used to take me forever to get signed in at the volunteer office The cursor moved everywhere on the screen except the correct numbers I needed. The more I used my left hand, the faster it got. Now I check in at the hospital in no time at all.
Finally January 1st 2014 came and my nephew arrived. His name is Caden Rex Jensen He has Hazel eyes very similar to my sister, and black curly just like his father. When I held my nephew for the first time, we both looked at each other and smiled. I thought about all the hard work I’d done in therapy to get to this special moment. The “pain and torture” was worth it. I thought. Caden Rex Jensen is now a year old and will soon have a sibling in August. I can’t wait until my nephew gets old enough to hear to this story. Then I can tell him, “I learned to use my left hand for you!”

“Write By Numbers”

The top photo is the lined paper Jessica used to help me learn to write. See the picture on the bottom left with the purple writing? That’s how my writing used to look before I started working with Jessica. I started working on this with Jessica in the middle of February and Traci’s birthday is March 31st. The book shows the finished product. Look at the improvement in a month’s time! Not Bad Huh? It was well worth it!

I never learned to write my name very well in grade school.  With cerebral palsy, it takes more time for me to learn something than the average person. I know what I want my muscles to do. Often, getting my brain to communicate with my muscles to work together is a challenge. My brain has to figure out how to re-route itself. Repetition is the key.
I did learn to write a little bit but just my name. I couldn’t write well enough for the teacher to read a whole sentence. There were other things to worry about in school. Time wise I had to use a one lined flat screen typewriter.  Recently, I learned how to write thanks to my good friend Jessica.
 It all started when I wanted to write my name in a book, I got my attendant aide Traci, for her birthday. It was one of those small pocket books that says, “To and from” on the inside. I just wanted to learn to write my name well enough and type a short birthday message, then paste it on the inside. However, Jessica had another idea. “Why don’t you learn to write the whole message?”
Jessica always pushes me to go to the next level!
“Are you crazy?” I asked.
“No Really. I think you can do it.”
 Jessica doesn’t take no for an answer easily! We only had a month and at the moment my name was barely readable. How would I ever learn in time for Traci’s birthday? Jessica and I have accomplished other milestones. I knew she wouldn’t suggest it if she didn’t think it was possible. I really wanted to give Traci a nice surprise, so I l hesitantly said, “Okay.”
We got to work right away. One of my biggest challenges was to get the letter c going in the right direction. My c’s we’re always backwards and I was taught to write my name in capital letters. As I was re-learning how to write my name, this time using a capital R and the rest of the letters lowercase, my brain connected well with different shapes.
A lowercase  c looked like a mini size cookie, h was like a chair, my name has to a’s in it so we made two c’s with kite tails,  the letter e is like a c starting with a line going down in the middle. For letters like c a, and e, Jessica said, “Start to the left and go all the way around. “ I learned most of the letters in my name start with the c motion.
One day Jessica brought in some lined paper with numbers and colors. It reminded me of when I was a kid and they have those coloring books where you color by numbers. I looked at the paper and asked,
 “What are we going to do? Write by numbers?” We both laughed. The paper was supposed to help me get the size of my letters right.  I did learn to write in time for her birthday and Traci loved her gift. I learned to write my name and a whole paragraph! What an accomplishment! I can write! I did it! Now, so I don’t forget how, the key is to keep practicing on a regular basis. Repetition, Repetition, Repetition.
 

 

 

 

Dear Awana Kids

Here’s another piece I wrote back in January when I took my flash fiction and nonfiction class. It’s a letter to my Awana kids explaining my disability and answering some questions they might have. Enjoy!

Awana Awards Ceremony T & T Girls  3-6th grade (Truth & Training) May 2013 at Grace Baptist Church

 

 
Dear Awana Kids,
I have cerebral palsy or CP for short. I was born this way. I had some problems at birth. Don’t worry it’s not contagious. CP is a condition not an illness. If I had a real illness I couldn’t be here. My wheelchair is nothing to be afraid of. I may look different on the outside but on the inside, I’m just like you.
            When I was your age I was in the Awana program just like you. I memorized the same bible verses you memorize, had similar Awana books just like you and got awards just like you. I was very good at memorizing. I got awards for my uniform almost every week.  I was one of the fastest memorizers! My mom was amazed. I turned out to be one of the kids who was the “crème of the crop” as the old saying goes. My body has cerebral palsy not my brain. I always say because I can’t write things down on paper I have to exercise a different part of my brain, which is why I have a great memory.  Some people have told me I have the memory of an elephant because I remember things so well! Have you ever heard the old saying, “An elephant never forgets?”
When you come up to me to make conversation with me, you don’t have to slow your speech down or talk to me in a loud voice. Just talk to me like you would anyone else. I can hear you and understand you. We don’t always have to talk about my disability.  I like to talk about other things too. What’s your favorite food? What about your favorite color? How about your favorite candy? My favorite candy is Snickers but I like anything with chocolate. I even have a shirt that says, “Drop the chocolate and nobody gets hurt.” I have quite a sweet tooth! Some people have called me, “Sweet tooth Rachael.” My favorite color is purple.  If you see me drop something on the floor, go ahead and help me pick it up. If we’re going outside somewhere, hold a door for me. I promise I won’t run you over!
If you have questions about the lesson, don’t be afraid to come up to me and ask me. I’m just as capable of answering your question as anyone else in the room. Again, my body has CP not my brain. I’m here to have fun with you and honor the Lord with my service the best way I know how. I’m really looking forward to some of the theme nights this year. Crazy hat night is one of my favorites. I think I’ll wear my Dr, Suess hat. “I do not like them Sam I am. I do not like green eggs and ham.” I’m really looking forward to a fun year at Awana of studying God’s Word with you and getting to know everyone better!

Love,
Rachael

 

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God’s Promise

 I had so much fun writing the poem about Saul I decided to write another one about Noah and the flood. I wanted to tell people what the rainbow means to me. A special thanks to my good friend, Sarah March. She was my extra pair of eyes as I wrote the poem. Your input was very valuable. Also, a special thanks to my brother-in-law, Cody Jensen. He gave me great direction in searching through the scriptures. I really enjoyed our conversation last week. Writing this definitely caused me to dig into God’s word more! The last couple weeks have been quite a journey! If you want to read the story of Noah in the Bible, it starts in Genesis chapter six, and ends with chapter nine, where the Lord talks about the rainbow, which is the emphasis in this poem. If you haven’t read the Bible, Genesis is the very first book. All scripture quotations are taken from the NIV. (New international Version). Genesis 9:12-15. Enjoy! 

I colored this picture last year at Joni and Friends Family Retreat when the  theme was, “Hope Overflowing.” As you read this, I pray your heart will overflow with the hope and peace of God’s Goodness.
 ““May the God of hope fill you with all joy and peace as you trust in him, so that you may overflow with hope by the power of the Holy Spirit.”  Romans 15:13
God was grieved by man’s sinful heart
So many people went their own way
Noah and his family were the few to obey
So God told Noah to build an ark
Soon a big flood would destroy the earth
There would be nothing left
Nothing left of worth
It wouldn’t be long
Before God’s creation was gone
But Noah and his family would be safe and sound
For following God’s ways they would not drown
Noah built the ark and brought in the animals two by two
The Lord shut the door and the flood began
For 40 days and 40 nights the rain came tumbling down
The Lord began to flood the ground
While those in the ark were safe and sound
Noah sent out a raven to find dry land
But he came back he found no safe haven
Noah sent out a dove
He found a green leaf
Everyone breathed a sigh of relief
The storm was through!
The earth made new!
A rainbow appeared in the clouds
And God said, “This is the sign of the covenant I am making between me and you and every living creature with you, a covenant for all generations to come: I have set my rainbow in the clouds, and it will be the sign of the covenant between
me and the earth. Whenever I bring clouds over
the earth and the rainbow appears in the clouds,
I will remember my covenant between me
and you and all living creatures of every kind.
Never again will the waters become a flood to destroy all life.”
The rainbow is more than a pretty little charm
It’s God’s Promise to keep us safe from harm
A beautiful reminder He loves the human race!
Thank You Lord for your Amazing Grace!


                                                                



 
 
 
 

                                                           

 
 

 

 

 

 
 
 
 


 

 

 

Summer Adventure 2015 Jesus Is Lord over His people

Last week I got teach the lesson at my table in fourth grade at Summer Adventure A.K.A. Vacation Bible School at Grace Baptist Church. The theme for the entire week was Jesus is Lord. Friday was Jesus is Lord over His people We told the kids the story of Saul. I wrote this poem and they loved It! I held their attention! I gave all my kids signed copies of the poem to help them remember the story and the fun week we had together! Another table leader shared it with her kids and soon everyone wanted a copy! It was a hit! Maybe I’ll have to start writing more poetry. Enjoy!

IMG_3458

Saul was a bully
Who tried to kill the holy
Slowly God worked on his heart
And Saul had a brand new start
After being blinded by the light
Ananias restored his sight
And Saul was filled with the Holy Spirit
And God used him with all his might
Even with a dark heart like Saul
God changed him and his name became Paul

 

 

 

 

“Focus On What You Can Do”

the great face off with Sarah March before the great Tortoise and the Hare race in front of my house October 2014. I’m the Hare Sarah is the Tortoise. I won! ! We just recently had anther race. I won again! Those pictures are on Facebook. Now I need to rewrite the Tortoise and the Hare story! 


“Focus On What You Can Do”
Here’s s a piece I’m posting this piece which I wrote for my Mircoflash fiction and nonfiction class I took in the winter semester. Enjoy!


“We would like to thank everyone for coming to our church play. We will now serve dinner and refreshments in the other room.”

Sarah brought me my walker and I stood up and turned around We followed everyone else into the other room. The room was on a lower level and we had to go down a long ramp to get to it. My walker has four wheels. If I don’t control my legs I can easily run right into something. Sometimes I need a little help.

“Now Sarah when we go down the ramp, hold the bar on the back of my walker so you can help me control the speed.”

I was anxious to get to the food!  Before Sarah had a chance to grab the bar, I pushed off at the top of the ramp, raised my feet in the air, and said “Catch ne if you can!” I laughed the whole way down. My walker went flying down the hill and Sarah ran after me. Finally, I got to the bottom of the hill. Sarah caught up to me. We both laughed and walked safely into the other room.

Having CP is hard at times. There are many moments when I wish it just wasn’t there, but, if it wasn’t for my CP, I wouldn’t need the help I need, and I would never meet great people great people like my friend Sarah. Funny moments of laughter like that wouldn’t happen. I’m able to show people how to have fun.  Without CP, some of the happy moments I have in my life wouldn’t happen. Whenever I get down about having CP, I have to remember my mother’s wise words. “Focus on what you can do not on what you can’t.”

“Uh-oh… Here Come Danger!”

 

Last Sunday would have been my dad’s  63rd birthday. This piece gives you a deeper insight into the man who said, ‘This is now the new normal,” as well as some of the fun summertime activities I’ve done. God gave me the gift of life, and I’m not going to waste a minute! Mom and Dad, thanks for surrounding me with so much love!

I walk on the wild side of life. If someone asks me, “Rachael, don’t you think this is a little dangerous?” I look at them with a big smile and with no hesitation, and I reply, “Hey, Danger is my middle name!” It makes people laugh when they answer, “Well then, go for it!” You could say it’s my slogan. People who know me really well exclaim, “Uh-oh. Here comes Danger. Look out!”

     I was born on February 8, 1983. My mother couldn’t quite put her finger on it, but she knew there was a problem. For some reason, she was very sick during her second pregnancy. This time, something was different. That particular day was her worst ever. She felt so bad; my dad was very hesitant to leave her alone.

     “Are you sure you’re going to be okay?” he asked.

     “Go ahead and go on with your day; I’ll be fine,” my mother insisted. “I just need to rest.”

     “If you’re sure,” my dad answered, “call me if you need me.”

     “I will. I promise.” My mother responded.

     “Okay,” he replied as he kissed her good-bye and walked out the door.

    Shortly after my dad left, my mother went over to visit with the next-door neighbor. While there, she called my grandma. Grandma knew what was going on. “You’re in labor,” she said. “We need to get you to the hospital right away!” Grandma hung up the phone, rushed quickly to the neighbor’s house, and there, paged my dad to meet them at the hospital.

     “What, labor already? How could that be?” thought my dad.

I wasn’t expected to arrive until April 8, which was two months away!

Once we got to the hospital, the doctor rushed my mom into surgery, and I was delivered by emergency C-section. However, when I came out of her womb, I had stopped breathing. Within fifteen minutes, the doctors were able to get no more than five breaths out of me. Imagine trying to hold your breath for 15 minutes! My skin was blue; I didn’t even make a sound – not even a faint baby cry. I was quiet, too quiet. My mother’s water had broken early causing me to become very ill. Two days later, the doctors realized I had pneumonia, and a lack of oxygen had caused serious brain damage. They tried everything medically possible, but my body just wouldn’t respond. No one thought I would survive. The doctors were about to lose hope, when, suddenly, they tried one more thing…antibiotics! I began to recover. Within 24 hours, they knew I would survive!

     Still, that didn’t mean I would go home right away. Because of complications, I weighed only three and a half pounds. Being underweight, my homecoming was delayed for another five weeks. Finally, I gained five pounds, and the doctors gave the okay for me to go home. Yet, the doctors’ visits weren’t over. They still had to closely monitor my condition. For the first year of my life, my mom took me back and forth every month to see about 10 different professionals.

     At this crucial time, my dad’s immediate response was, “This is now the new normal.” He knew it was going to be hard, but he was so happy and relieved I came out alive, and I was coming home at last. He was willing to do whatever it took to take care of me.

      When I was three months old, my condition was finally diagnosed. Dr. Faulk announced to my mother, “Mrs. Benson, Rachael has cerebral palsy.” Stunned, she just sat there listening as he continued to explain. “We need to get her connected with the Regional Center right away so you can get therapy for your daughter.” ”The sooner you get the right kind of help, the better it will be for Rachael in the future.”

“Thank you,” my mother replied as she shook the doctor’s hand and quietly left.  She drove home in silence. She couldn’t believe what she had just heard.

     Arriving at home, my Dad saw the look on my mother’s face. “What happened?!” he asked.

      Mom replied, “The doctor finally confirmed Rachael’s diagnosis… she has cerebral palsy!  He wants us to connect with the Regional Center so we can get her therapy.”

Sensing my mother’s fear, my father placed his hands firmly on her shoulders and said,    “Well…we’ll just have to take care of it! We’ll just do whatever we have to do!”

     Today, 28 years later, the legacy of my father’s strong leadership and courage still carries on in my family’s life and mine. My father and mother bravely pulled together and built the firm foundation upon which I “dangerously” approach my life.  A “Woe is me, I’m disabled” attitude has never been allowed. Whenever I start to get bitter about having this disability, my mom reminds me to focus on what I can do rather than on what I can’t.

     When I was a child, our favorite family activity in the summertime was water skiing. While everyone else skied standing up, I skied with my legs extended behind my torso on a skibob to avoid direct vein constriction and hip socket displacement. If you knew anything at all about CP, you knew sitting on your legs, the “W” position, was what the doctors and therapists warned against.  Even if I had to do it differently, I skied, and I loved it! I was still able to be part of the family and participate in the family activity.

       Today, when doing many athletic outdoor activities, such as, cruising along tops of trees riding the zipline, climbing all the way to the very peak of a rope’s course, swimming free as a fish underwater, flying high in the sky in a hot air balloon, dancing the night away twirling in my wheelchair, or pecking on the keyboard composing one of my stories, you might ask, “Rachael, don’t you think this is a little dangerous?”

      P-leeeasee!!!! If I survived my birth, I can survive anything!! I may have entered the world quietly, but I’ve now made up for it! So, if you hear my chair humming down the street, don’t try to stop me! Remember, “Danger is my middle name!” A.K.A. Rachael “Danger” Benson!

The Story Behind “Rudolph The Red-Nosed Reindeer”


You know Dasher, and Dancer, and Prancer, and Vixen, Coment, and Cupid, and Donder, and Blitzen, but do you recall the most famous reindeer of all….”  Sound familiar? You know the rest of the words right? I’m sure you do. It’s a famous Christmas Carol. However, I’ll bet if I were to ask you, “Where did the idea for Rudolph come from–you wouldn’t know the answer, would you?” What is it that makes the beloved reindeer so famous? What could the people of the world possibly have in common with an animal that is said to be the leader behind Santa’s sleigh one night out of the year?
It all started with a guy named Bob May. His wife was dying of cancer. His 4-year old daughter sat on his lap and cried. “Why isn’t Mommy just like everyone else’s Mommy?” She asked. His daughter’s question reminded him of his own childhood. Bob May was small as a kid. He was too small to compete in sports. He was often picked on and bullied by other boys. He was the kind of person who never did quite fit in very well with things.
This all happened during the time of the great depression in the 1930’s. Since he couldn’t afford to buy a Christmas gift, he decided to make one. In an effort to try to comfort his daughter, he wrote a children’s book. He told a story with animals. Rudolph was the story of his life in fable form. Rudolph was an outcast just like his creator, Bob May. Rudolph was a reindeer with a shiny nose. He finished the story just in time for Christmas Day.
Soon, the general manager of Montgomery Ward heard about the storybook and offered Bob May a nominal fee to purchase the rights to print the book. The story went to print and was given to children who were visiting Santa Claus in stores. By 1946, six million copies of Rudolph had been distributed and sold. Soon, toys followed and Bob May was able to make a living and comfort his grieving daughter at the same time.
It was his brother-in law, Johnny Marks, who adapted the story into the well-known song we sing today. Although turned down by many singers, the song was released in 1949 and sung by Gene Autry. It became a phenomenon and sold more records than any other song with the exception of  “White Christmas.” Like May, Rudolph learned that being different can be a blessing.
            Although this song doesn’t have any reference to Christ, we can all learn a lot from Rudolph and his creator. Often, we try to fix the things we don’t like about ourselves-our gray hairs, our wrinkles, etc, as if something about ourselves is a mistake. In Psalm 139, beginning in verse 13, the Bible says, “For you created my inmost being: you knit me together in my mother’s womb. I praise you because I am fearfully and wonderfully made…” If people were created in their mother’s womb, how could anybody possibly be a mistake? At the very end of verse 16, it says, “Your eyes saw my unformed body; all the days ordained for me were written in your book before one of them came to be.”
The bottom line: If we were all made the same, there would be no creativity. We wouldn’t have anything to learn from each other because there would be no need for growth. When we try to fix the things we don’t like about ourselves, we’re telling God, our creator, He made a mistake-the very same God who created everything else before us.
 We all have special gifts and talents that have been given to us by God. The question: What will we do with them? Will we be like Rudolph and learn to use them wisely, or will we be like the man in the Bible who buried his one talent and tried to forget all about it? How will you serve the Lord in the New Year?
Dear Lord,
As the New Year approaches, please help me find new ways to use my gifts and talents to serve you.
Amen
* Information taken from www.urbanlegends.com.
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Therapy dog helps patients at hospital

Therapy dog helps patients at hospital
Hey everyone! I didn’t write this, but here’s an article I found in The Signal about how I helped inspire someone else in a wheelchair to volunteer at the hospital. The writer doesn’t mention my name, but I’m certain that they talking about me because I’m the only one there in a wheelchair who volunteers. They do talk about a young girl with cerebral palsy who pushes around a magazine cart. Here’s an example of what can happen when we let our lights shine for Jesus. Enjoy!

Danger and Zippy: A weekend At Oakbridge


Danger and Zippy:  A weekend At Oakbridge
Thursday, August 25
Hey, everyone, Zippy here. I’m Rachael’s wheelchair. Fun Life campers and I just got back from an adventurous place called Oakbridge.  Fun Life is a Christian organization for people with disabilities. I wish, I could talk about everything we did, but I’m just going to share with you some key highlights. Are you ready? Hold on tight. It’s going to be one wild ride. Here we go! HONK! HONK!
 At Oakbridge, the fun began right away. As each camper got off the bus, the welcoming camp leaders clapped, cheered, and yelled our names. It was very special…especially for “RACH-AEL! RACH-AEL! RACH-AEL,” my rider.  It was a big parade! I didn’t dress for the occasion, oops.  
Next, we headed to the dining hall. The camp leaders gave me the royal treatment-wheelchairs first! I like first class. Then, we saddled up to the table. Rachael had tacos, and I had a couple squirts of WD40, yum!
     Soon, it was time to head for the clubhouse. The speaker spoke about being lights for Jesus that point people to God. To illustrate, the room grew dim (I need headlights), then lit up once again. The message ended, and we headed to our cabin. Inside, Rachael parked me next to her bed, plugged my battery into the electric socket, and together, we dreamt about tomorrow’s adventures.
Friday, August 26
  Up early, Rachael buckled in, snapped my footrests into place, and off we drove to the dining hall. I heard Rachael say that the egg and sausage burrito was “yummy.”
At club time, the speaker told the story about the Good Shepherd. Our camp leader gave us journals. Rachael wrote:
“BACK HOME, I CARE FOR THE PEOPLE AT THE HOSPITAL. I PASS OUT MAGAZINES AND SMILES.”
She sure does care. Back home, the hospital is one of my favorite places to go with her. I love seeing the impact Rachael has on others. When they see her ride up, they realize their life doesn’t have to stop because they are in a wheelchair. Rachael and I are both good shepherds to each other. I take her where she needs to go, and she makes sure my parts are maintained so I function properly.
   That evening, the camp had a carnival on the field. Rachael won five tickets, enough to “pie a leader” in the face. She “pied” camp leader Randy because he had a beard and the shaving cream stuck to him quite well! She giggled and I could tell she enjoyed it.
Saturday, August 25, 
The campers put on their white t-shirts.  They were told to wear something they didn’t mind getting dirty. “Uh-Oh, This sounds dangerous,” I thought.   
 We played two games, first, Chariots of Fire. A rope attached to a sleeping bag was tied to my wheelchair handles. With Rachael driving and me as the chariot, we dragged campers around cones! Second, we played a chalk game. Little did I realize what was coming-up. The leaders gave campers handfuls of colored powdered chalk, and told them to throw it at each other. Next thing I knew, all kinds of colors were coming at us! Chalk was getting all over my controls, my footrests, my handles-everywhere! Not only were the colors on me, but, also, on Rachael’s shoes, pants, t-shirt, and hair! She was more colorful than I’d ever seen her before! That’s when; I nicknamed her “Danger.”
 After lunch, “Danger” scaled the rope course and zoomed across the zip line. The camp leaders put her into a special harness that took her up the ropes and throughout the course.  She really stood out in all those colors! At the zip line, before she launched, “Danger” yelled, “THREE, TWO, ONE, BLAST OFF!” She zoomed down the zip line giggling and smiling the whole way.
 That night, we had a spectacular Neon Dance! Everyone danced the night away by the light of glow sticks. 
Sunday, August 26, 
            Time to head home. We were asked what two things we would take home from camp. Danger yelled, “The color duel.” “Me, too!” I thought. “I’m still wearing the colors!”  And, I would like to wake up early as I did at camp.”   
When we arrived home, “Danger’s” mom saw the rainbow of colors painted all over me. “This is what happens at Fun Life Camp!” They both chuckled. 
 Mom washed most of the colors off, but some remained. That’s okay. It was fun!! I can’t wait to see what we do next. Living with “Danger” is always an adventure! 
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