Bald Big Brother

New To Alopecia…
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Want to talk to someone who has already walked in your shoes?
Boys/Young Men/Young Adult

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What We Do

Connect. Share. Bond.

This is a platform to help each other deal with and Thrive living with Alopecia

Identity

Who you ARE is not tied to your spots or lack of hair

GRIT

It isn’t easy… but GRIT can help you in hard times

Self Worth

Every person has self doubt because of their perceived differences

Look in the Mirror

When you gaze in the mirror, let your inside passion shine through

Meet the Visionary Behind Bald Big Brother – Triple B

For Me It Started before I remember. I have seen the pictures of my hair, but I actually do not remember a time when I had hair.

As the story goes, my first spot happened before my first birthday. After the local doctors had their suspicions my parents eventually took me to University of Minnesota to Dr. Maria Hordinsky for my official diagnosis.

I had one shed/growth/shed before my parents shaved my head bald before my Third Birthday… and other than a few fuzzes here or there, it has never grown back.

I am here today, trying to show other kids/teens that life can move forward in positive ways even though we may look different than most people in our circles.

My name is Brogan Borst and I will graduate Culver Military Academy June 2025, and I am looking to help others while I help myself in this journey of dealing with alopecia.

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“I have had Alopecia since I was a baby.  First, it was patchy, then I lost all my hair when I was 3.  Now I don’t have hair, eyebrows or eyelashes.  I sometimes don’t like that I have Alopecia because kids make fun of me and call me weird.  I don’t want people to see that I don’t have hair, which is why I wear a skull cap most of the time.”

-Brogan Borst (at age 10)
Lead BBB

Connect. Share. Bond.

You are Not the First

Even though you may not know anyone with Alopecia, millions of people have gone before you. Don’t let this affliction change your course… and learn how to use it to propel you beyond your wildest dreams!

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Latest Articles

  • being bullied ~ because of alopecia universals

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    admin

    I’m truly sorry to hear that you’re experiencing bullying due to alopecia universalis. It’s essential to recognize that you’re not alone in facing this challenge. Alopecia areata, especially in children and teens, can indeed make individuals targets for bullying. Here are some insights and coping strategies: Remember, you’re strong, resilient,…

  • Living Unlabeled: A Teenager’s Journey with Alopecia Universalis

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    admin

    By Alex, age 16 Introduction In a world that thrives on labels and categories, I’ve always felt like an outlier. My name is Alex, and I’ve been living with alopecia universalis since I was a baby. For those unfamiliar, alopecia universalis is an autoimmune disorder that causes complete hair loss…