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Fighting for Every Pointand Every Breath

Christian is one of the best 12-year-old basketball players in California. He also has cystic fibrosis, a dangerous disease that makes it hard for him to breathe. What’s that like? Read on to find out

Slideshow

Gregg Segal

Gregg Segal

For the Love of the Game
Christian plays basketball on a top travel team. He takes many medicines to treat his disease—but he still gets tired faster than other players. 

    Every single morning, Christian Collins wakes up an hour earlier than his friends and puts on a special vest

    Why? He’s not trying to make a fashion statement. His life actually depends on it

    Christian has a serious disease called cystic fibrosis (CF). It causes a thick, sticky mucus to build up in his lungs. The mucus can cause infections and makes it hard to breathe.

    That’s where the vest comes in. It’s hooked up to a machine. When Christian turns the machine on, the vest inflates. Then it vibrates like crazy. The vibrations help loosen the mucus in his lungs, so he can breathe better

    It’s one of the many steps Christian takes every day to fight his disease.

Living With CF

    How did Christian get CF? It isn’t a disease youcatch—you’re born with it. CF has no cure, and it usually gets worse asa person gets older

    To stay healthy, Christian uses his vest at least twice a day. He also breathes through a tube that delivers medicine as a mist. And he takes more than a dozen pills daily

    Still, he coughs a lot. His coughing fits can be so bad that he has to step out of class at school. That happens about once a day

    CF also makes Christian more likely to get ill. Last year, he had to go to the hospital after he got a dangerous infection called pneumonia. He was so sick that he missed almost a month of school.

A Regular Kid

    Christian faces some big challenges. But in many ways, he’s just like every other kid. He’s talkative and funny and one of the tallest kids in his grade. He loves eating barbecued ribs and hanging out with his dog, Joker.

    Christian’s favorite thing to do is to play basketball. He has been playing since he was 5 years old. It’s not easy, because his lungs don’t work as well as other people’s. Imagine running up and down the court while breathing through a straw. “I get tired a lot faster than everyone else,” he says. “That just means I have to work a lot harder.” 

    During basketball games, Christian uses a device called an inhaler. It sprays medicine into his lungs. But sometimes, he still can’t catch his breath and has to take a break. “My chest feels all tight and clogged,” he says. “I’m trying so hard to breathe that sometimes I just start sobbing.”

The Big Moment

    Last year, Christian was picked to play on a travel basketball team. He was thrilled. He knew it was a chance to prove that CF can’t stop him from competing with the top players.  

    Christian’s big moment came in March 2019. His team was playing one of the best teams in the country. If Christian’s team won, they would go to the championship

    With a few seconds left, the score was tied. Christian got the balland he didn’t hesitate. He didn’t worry about his lungs. He drove down the court quickly and tossed in the game-winning shot

    Christian was named Most Valuable Player (MVP) of the game. Afterward, his team won the championship. The next week, his name was included on a list of the top 40 players his age in California. “I was like, ‘Oh my God, I’m ranked,’” Christian says

Courtesy of family 

All Hooked Up  
Christian spends an hour a day using a machine that loosens the mucus in his lungs.

Teaching Others

    Sometimes, the kids at school ask Christian insensitive questions. They have asked if he’s going to die soon and why he coughs so much. Once in a while, someone is just plain mean

    Not long ago, Christian got in a fight with a classmate who said something cruel about his illness. Both boys were sent to the school counselorwho asked Christian to tell the boy about living with CF. So Christian explained about his special vest, the hospital stays, and his many medicines

    “While I was talking, the other boy started crying,” Christian said. “He kept saying, ‘I’m sorry. I didn’t know. I didn’t know.’”

    Now Christian wants you to know: People who may seem weak can be so much stronger than you think

ACTIVITY
Cause and Effect

Courtesy of family 

Winning Smile
Last year, Christian was named MVP of a very important game.

You’ve just read “Fighting for Every Pointand Every Breath.” Now it’s time to do this activity.

Tip: A cause is what makes something happen. An effect is what happens as a result.

What to do: To understand how one cause can have many effects, answer the questions below using details from the article. We did the first one for you. 

The Cause:

Christian was born with a disease called cystic fibrosis (CF).

Effect 1: 
CF causes a thick, sticky mucus to build up in Christian’s lungs.

Effect 2:
HintWhat can happen to Christian because of the mucus in his lungs?

Effect 3:
Hint: What must Christian do to stay healthy?

Effect 4:
Hint: How does having CF affect Christian on the basketball court?

Effect 5:
Hint: How do kids at school treat Christian sometimes?

videos (1)
Video

True Teen Story

My Story: Christian Collins

A 12-year-old basketball star talks about life with cystic fibrosis.

Leveled Articles (2)
PDF

True Teen Story

Higher Level: Fighting for Every Point—and Every Breath

Read or print a 800L-900L version of this article in magazine view.

PDF

True Teen Story

Lower Level: Fighting for Every Point—and Every Breath

Read or print a 500L-600L version of this article in magazine view.

Text-to-Speech