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Spreading the 91Ƶno hair, don91Ƶt care91Ƶ attitude

Makayla Krenzel is spreading awareness about her disease and participating in dance competitions.
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Makayla Krenzel, 10, with sister Cruz, eight. Makayla has been spreading awareness about her disease as a Canadian Alopecia Areata Ambassador and is participating in dance competitions with the Lake Country School of Dance. (Carli Berry/Capital News)

Don91Ƶt be afraid to be yourself.

That91Ƶs the message Lake Country residents Makayla Krenzel and her mother, Becky, are sharing.

When Makayla was two, she was diagnosed with the auto-immune disease Alopecia Areata, which caused her to lose her hair.

Now, the Aberdeen Hall Preparatory School student is a Canadian Alopecia Areata Ambassador, spreading awareness for the disease.

91ƵIt91Ƶs a very self-conscious thing. We identify ourselves with the way we look,91Ƶ said Becky.

But it didn91Ƶt stop Makayla from being herself. She91Ƶs an active dancer and refuses to wear a wig.

She finds them itchy, she said, and will be dancing bald in her upcoming solo performance with the Lake Country School of Dance in Vancouver Feb. 10 and 11.

The dance studio wanted Makayla to wear a wig, but she refused.

The company Liberty and Grace is donating wigs for the performers, so Makayla agreed to wear one if the other girls did, said Becky.

91ƵShe said 91Ƶmom I don91Ƶt like the way they feel. This is the way I am mom, why would I change?91Ƶ I think that91Ƶs the biggest thing, I think she doesn91Ƶt feel comfortable,91Ƶ said Becky.

The competition is called Velocity, and she will have the opportunity to perform in Las Vegas if she makes it to the next round.

The 10-year-old is also trying out for Team Canada, which will be performing in Germany.

Becky said it91Ƶs good for Makayla to experience the world.

91ƵLiving in Kelowna you91Ƶre kind of in a bubble91Ƶ (when) you91Ƶre out of your element you realize how many people are looking at you, so with Team Canada (it was a big step for her.)91Ƶ

Makayla won91Ƶt see if she made the team until the end of February.

But, with the help of friends and family, she holds her head with pride.

91ƵI have good support,91Ƶ said Makayla.

Her younger sister Cruz, will joke with her and tell her to do her hair in the morning.

While Makayla isn91Ƶt bullied, she finds it irritating when people want to touch her head, she said.

Becky is a also an Alopecia Areata group support leader in the Okanagan after she realized there weren91Ƶt support groups.

91ƵPeople look at her and (assume) she91Ƶs got cancer,91Ƶ said Becky, aiming to provide support for people with similar cases like Makayla91Ƶs.

Becky plans to hold a support group in March at the Rutland Library.

To follow Makayla91Ƶs journey find her on , and .

See about Makayla.





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