Barrier Breaker of the Month

Barrier Breaker of the Month is our way of celebrating the courage it takes to show up authentically in a world that doesn't always understand visible or invisible differences.

Each month, we spotlight an individual living with an autoimmune condition and share their story across our website and social platforms. Our goal is to amplify real voices, celebrate uniqueness, and remind others that they are never alone in their journey.

Every story shared is a reminder that beauty is not limited by difference. It is strengthened by it.

April 2026

Meet Nataly Ruiz

Our April Barrier Breaker: A 16-year-old embracing alopecia with confidence, creativity, and courage

Nataly Ruiz - Barrier Breaker April 2026
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Her Story

At just 16 years old, Nataly is already a powerful example of confidence, resilience, and self-expression. A lover of theatre, choir, and spending time with friends, she brings creativity and joy into everything she does. But one of the most meaningful parts of her story is how she has learned to embrace alopecia and proudly celebrate who she is.

Nataly was diagnosed with alopecia in August of 2019 when she was only nine years old. At the time, the diagnosis brought a wave of uncertainty and fear. Her mom explained the different types of alopecia and the possibility that she might eventually lose all of her hair. It was a difficult moment for both of them, and they remember crying together as they faced the unknown.

The early part of Nataly's journey felt like an emotional roller coaster. Losing her hair brought new experiences and challenges including moments of self-doubt and bullying that she didn't fully realize at the time. One of the hardest parts, Nataly says, was learning to love the new version of herself. Looking in the mirror, she searched for confidence that sometimes felt out of reach.

But with time things began to shift. During the COVID-19 lockdown, Nataly lost the rest of her hair. While this could have been another painful moment, it also became a turning point. As the world slowly returned to in-person life, Nataly started embracing her bald head with growing confidence.

Today, she proudly lives without wigs, only wearing them occasionally as a fun accessory. In fact, she says her bald head has become her favorite thing about herself.

Finding Community

A major part of that transformation came from finding community. Early in her journey, Nataly's mom discovered the Children's Alopecia Project (CAP), an organization that supports young people living with alopecia. At first, Nataly attended with the hope of finding ways to "fix" alopecia. Instead, she discovered something far more meaningful: acceptance.

Through CAP and events like the Baldtourage Summer Soiree, Nataly met other girls and women who proudly embraced their baldness. Seeing their confidence helped her realize that she didn't need to be fixed and was already beautiful exactly as she was.

Another important part of her journey has been building a strong support system. Nataly credits her friends, her best friend, her mom, and her boyfriend for standing by her side. Having people who can navigate the stares and curiosity that sometimes come with being seen as "different" has made all the difference.

Creativity & Self-Expression

Nataly also hopes people understand that alopecia is about far more than hair. "There are so many layers to alopecia that people don't see." From identity struggles to navigating social interactions and living with an autoimmune condition, the experience can be deeply emotional and complex. But through it all, Nataly reminds herself that she is strong, beautiful, and proud of who she is.

Creativity has also played a huge role in her self-expression. As someone passionate about acting, Nataly loves exploring emotions through different characters. Acting allows her to connect with herself while stepping into other perspectives.

She also loves makeup, especially clown makeup, which she sees as a form of artistic freedom. To Nataly, makeup becomes another way to celebrate individuality. If her body has made her into a unique and beautiful piece of art, she embraces the opportunity to add to that art with color, creativity, and expression.

When asked what alopecia has ultimately given her, Nataly describes it in one word: "freeing." Becoming bald has changed the way she sees the world and the way she sees others. It has helped her appreciate the beauty in everyone's uniqueness and celebrate the courage it takes to embrace what makes us different.

Message to Others

"Allow yourself to feel your emotions. It's okay to cry or feel angry because those feelings are part of grieving your previous self. But don't stay there. Let those emotions guide you toward learning more about yourself and building confidence in who you are."

Messages from Friends

"Throughout my entire time knowing her, she has been nothing but loud and proud about her alopecia. No matter what crosses her path, she never wavers and continues to be confident in herself and what she has and that is why she is a barrier breaker."

Micah (Nataly's Boyfriend)

"Nataly Ruiz is one of the strongest and most inspirational people I know. She's had alopecia since she was nine years old, and she's since grown up to be someone extremely proud and confident in who she is."

Juliet (Best Friend)

"She's not afraid to be bald, and educate people on how she got there. She doesn't just sit down and take an insult, she stands up and teaches people why they thought that would hurt her. In the face of adversity, she's a shining sun who loves every asset of herself."

Hannah (Best Friend)

Inspired by Nataly's story? Know someone who should be our next Barrier Breaker?

✨ Featured May 2026

Meet Micah Joy

Our May Barrier Breaker: A 23-year-old who refused to accept "no remaining options" and became the second person in the world to receive a groundbreaking Lupus treatment

Micah Joy - Barrier Breaker May 2026
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Her Story

In 2020 she woke up feeling sick, and that feeling never went away. Micah Joy is 23 and currently in teachers college, but her journey over the past six years has been anything but typical. What followed that feeling were years of uncertainty, worsening symptoms, and treatments that didn't work. She began her studies at Western University in 2021 on a basketball scholarship, determined to keep pushing through despite everything.

As her health declined, she eventually reached a point where she could no longer walk independently and had to step away from the sport she loved, an experience that deeply impacted her sense of identity. After four years without answers and being misdiagnosed with severe JIA, Micah was finally diagnosed with severe treatment-resistant Lupus in 2024.

"It was a weird mix of relief and grief. I was so grateful to finally know what was going on but it was also really hard to hear."

Refusing to Accept the End

Despite the challenges, Micah continued to show up for herself. She graduated in 2025 with an Honours Specialization in Chemistry with Distinction and completed research she is incredibly proud of, something that gave her a sense of purpose during one of the hardest periods of her life.

After being told she had no remaining treatment options in Canada, Micah refused to accept that as the end of her story. She began researching on her own and connecting with researchers around the world, which ultimately led her to a groundbreaking BAFF CAR-T cell therapy clinical trial in the United States.

In February 2026, her stem cells were collected and genetically modified. On March 9th, just one day after her birthday, she received her stem cell transplant, a day she now calls her "rebirth day." Micah is the first Canadian and only the second person in the world to receive this treatment for Lupus.

Now in recovery and already seeing improvements, she is holding onto something she hadn't felt in a long time: hope.

Redefining Identity

One of the biggest challenges throughout her journey has been losing her sense of identity. Over time, she has learned how to redefine herself and find confidence in who she is.

"Living in a sick body is complicated, but I've learned that real beauty is in things like kindness, strength, and resilience. I can't control my health, but I can control who I am."

Micah credits her support system as everything: her family, friends, and the chronic illness community who showed up for her in both big and small ways. She also formed a meaningful connection with the only other person in the world to receive this treatment, reminding her that even in the rarest of experiences, you are never truly alone.

While she had to step away from playing basketball, she found a new way to stay connected through coaching, continuing to give back to her community and hold onto something she loves. Through it all, she has learned to find joy in the simple things: a good coffee, a hot shower, time with her one-year-old nephew and her three sisters.

Message to Others

"This sucks and you're allowed to feel that. You don't have to be positive all the time. When things are really hard, just focus on getting through one hour at a time."
"For a long time it was, 'I can't believe this is my life.' Now it's, 'I can't believe I made it through all of that.'"

Inspired by Micah's story? Know someone who should be our next Barrier Breaker?