Junior seeks to educate about syndrome

By Rachel Scall
Updated: 11/05/10 1:50pm
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Michael Crosa, a resident adviser mentor in Morrison Residence Hall, leads a drum circle. Playing instruments helps people with Tourette’s syndrome control their tics.

 

Crosa works at the front desk in Morrison. When he can, he tries to educate himself and others about Tourette’s to spread understanding.

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Close ups: More than just Tourette's

  Close ups: More than just Tourette's

This installment of Close ups looks at Michael Crosa, a junior psychology and music double major who has Tourette’s syndrome — and homework, a job and a passion for music.

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It is as if a fly landed on his cheek.

The left eye scrunches, then the right. Three quick shakes of the head and the entire tic is over in less than a second.

Michael Crosa, a junior psychology and music double major, has Tourette syndrome, a neurological disorder characterized by involuntary, repetitive sounds and movements.

But Crosa also has a full course load, a job as a resident adviser mentor and a passion for music.

“It’s a part of me. It’s there,” Crosa said of his Tourette’s. “But there is a lot more to me and that’s who I am.”

Crosa developed Tourette’s at age 16 after complications developed from an indeterminate virus he contracted at school.

“It traveled north to my brain and did some work,” Crosa said.

One day during junior year, after Crosa had finished lunch and returned to his algebra class at Asheville High School, his arm shot out to the side.

“I was thinking about like, ‘Am I doing this?,’” he said.

After school, Crosa visited the emergency room at Mission Hospital in Asheville where doctors were stumped as to why Crosa was having involuntary tics.

The doctors referred Crosa to Emory University Hospital in Atlanta, but doctors there were still unable to diagnose the problem.

It was only after five months of working with doctors at the National Institutes of Health in Bethesda, Md., that Crosa was finally diagnosed with Tourette syndrome.

“When I actually found out I had Tourette syndrome it was really relieving,” Crosa said.

Waiting for a diagnosis wasn’t easy for Crosa’s family.

“It was very scary,” said Melissa Robinson, Crosa’s mother. “They were talking about whether it was brain tumors.”

But Crosa said he was happy with his family’s reaction and appreciated their support.

Because he developed Tourette’s so late in life — Tourette syndrome is usually diagnosed at a younger age — Crosa said he had to find a way to reconcile an identity he had already developed with a disorder that would affect his future.

“I very much felt like I was Michael and Tourette’s was tacked on,” Crosa said.

This difficulty manifested itself during Crosa’s resident adviser training his sophomore year at UNC.

Each RA was asked to list 10 personal characteristics and then cross several off at a time, leaving each with the one characteristic that supposedly described them best.

Crosa was left with the word “Tourette’s.”

“It was the first time I had really cried about it and I bawled about it,” he said. “It was a big emotional moment for me.”

But Crosa said that after this emotional breakdown, he was able to come to terms with his Tourette’s.

“I feel like I’ve really accepted it,” Crosa said. “I’m Michael who happens to have Tourette’s, as opposed to Michael plus Tourette’s.”

Now one of Crosa’s goals is to educate himself and others about Tourette syndrome.

People are more accepting of the disorder when they understand it, Crosa said. He said this makes him less self-conscious.

“He’s very, very open about it,” said Daniel Stellini, a first year graduate student and friend of Crosa.

Learning about Tourette’s has also helped Crosa learn to partially control his tics.

“One of the biggest treatments for Tourette’s is education,” he said. “The more that you know about it, then the more likely you are to be comfortable and understand what’s going on.”

Another treatment for Tourette’s is music — something Crosa has been passionate about since the sixth grade.

“If someone is playing an instrument, they won’t have a tic or they will have a lot less tics,” Crosa said.

Crosa is a percussionist in his music classes, but his favorite instrument to play is guitar, he said. Growing up, he played the guitar with his father.

This past summer, Crosa worked at Camp Twitch and Shout, a camp for children with Tourette syndrome, where he was a music instructor. He led drum circles and other music-related activities for campers.

“I discovered music therapy and that’s something that I want to go into,” he said.

Crosa sees his Tourette’s as a building block, not an impediment, he said.

“I feel like I’ve used Tourette’s to improve myself and improve my life goal and life direction,” Crosa said.

People around Crosa notice his positive attitude regarding Tourette syndrome.

“I have honestly never seen him get frustrated about it,” said Jillian Dahl, a sophomore psychology major who became friends with Crosa her freshman year.

Robinson said she is proud of all that Crosa has accomplished and his plans for the future.

“He had the option of withdrawing from school and he didn’t choose to do that,” she said.

“I just think it’s really amazing the way that he handled it.”

Contact the University Editor at udesk@unc.edu.

Published November 4, 2010 in Campus

2 comments

RMcMeezy
November 5, 2010 at 9:23 AM
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Interesting and informative article, and I wish Crosa the best.
That said, I wonder if we will see a letter titled “Tourette’s Guy Costume Makes Light of Tourette’s Syndrome”. One of my friends definitely dressed up as the character from the viral video, so should this get the same treatment as the Antoine Dodson costumes?


John Bobo
November 8, 2010 at 10:46 PM
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When we hear about diversity, we often hear discussions about race, sexual orientation, and the like. I have been appalled at how those living with Tourettes have been treated, particularly children in school. People like Michael are working to change perceptions and attitudes. We need more people like him!

 
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