Getting Bullied Wearing Wigs

Growing up with alopecia felt like a battle I could never escape.

It was something I tried so desperately to hide — but everyone could tell.

The wigs I wore as a child looked artificial. There was no denying I had one on.

At school, kids teased me. They’d mock the way my hair parted — “Why does your hair grow in a circle like that? Are you wearing a wig?”

All I could manage was a soft “no,” shaking my head.

Because the truth was unbearable.

I couldn’t accept my own diagnosis, let alone let others know.

They’d think I was gross.

They wouldn’t want to be my friend.

They’d hate me.

So, I told myself: My best chance at belonging is if no one ever finds out.

I just wanted to be normal.

I remember one time, a soccer ball was deliberately kicked at my head — an attempt to knock my wig out of place and “prove” their suspicions.

When it happened, I calmly walked to my gym teacher and asked to go to the bathroom. I didn’t look him in the eye — I was too embarrassed. But he knew. He let me go.

I rushed into the stall and fixed my hairline as quickly as I could. Then I walked back into the gym like nothing happened. I didn’t face anyone. I didn’t say a word.

I just kept pretending I was normal. That my hair was real. That I belonged.

There was another time — a cruel game made up at school. The goal was to expose whether the latest rumor about someone was true.

For me, the rumor was that I wore a wig.

The game was this: one person pulled another’s hair until they yelled “ouch!” — the idea being if you didn’t feel it, it must not be real.

I had no choice. I played along. I screamed “ouch!” at what I guessed was the right moment, even though I didn’t feel a thing.

But I knew the truth.

I hadn’t fooled them.

The giggles after the soccer ball, the whispers in the hallway — they knew.

Still, I kept showing up. I kept going to events, hanging out with friends, attending school, doing everything I could to prove that I was “just like everyone else.”

I denied the teasing, denied the questions, prayed someone would change the subject when it came up.

Because if they found out, I would be a freak.

And I just wanted to be accepted. Understood. Liked.

What It Took to Finally Tell Someone

It wasn’t until years later, through therapy, that I started confronting the pain I had pushed down for so long.

Therapy forced me to speak about things I had buried — and in doing so, I started using my voice again.

I became accountable for my own healing.

And healing meant speaking up.

Sometimes that meant having hard conversations with the very people who hurt me.

I found that writing things down helped. There was something therapeutic about putting pen to paper. It gave me clarity — and courage.

When I had to say those words out loud, I read from the page. It kept me grounded. It helped me get through it without freezing up, softening the truth, or losing my train of thought.

Reading from a letter meant I didn’t have to make eye contact. I didn’t have to read their expressions. I just had to get through it — my truth, uninterrupted.

Some people had no words in response but appreciated the honesty.

Others were thankful to understand me better, and respectfully asked for time to process.

That was enough.

Because once I said it — I could breathe again.

And little by little, the things that once triggered me… stopped happening.

And if they did happen again?

I had the right to speak up.

I could say gently, “Hey — that actually hurts me. Can you not do that?”

That’s what healing looks like.

That’s what reclaiming your power feels like.

Learning to Speak Up

Over time, I started saying how I felt more often. I started saying “no” when something didn’t feel right.

I spoke up when I disagreed, voiced my opinions, even chatted with strangers.

And eventually, I found myself sharing about my alopecia — for the first time — with someone new.

It was a hairdresser. I knew they’d figure it out anyway. But instead of hiding, I chose honesty.

What followed blew me away.

They shared stories of other clients with alopecia. They told me about their journeys, what worked for them, how they coped.

I offered my own tips — advice I wish I had known sooner.

And I left the salon inspired. Energized. I imagined another girl hearing those same tips I’d just shared. I imagined her feeling a little more hopeful.

And that’s when it hit me:

My pain, shared honestly, could actually help someone else heal too.

Why I’m Writing This

I still struggle with words.

I still stumble when I speak, still feel guilt for expressing myself.

But this blog has become my safe space.

My outlet.

My voice.

If you’ve read this far — thank you. Truly.

You’ve given me the gift of being heard.

For the recovering hearts,

Jenna

If this story resonates with you or someone you know, I’d love to hear from you. 💌 Drop a comment, share your story, or send a message — let’s create a space where we feel seen. 🫶🏻

What It Felt Like to Be Misunderstood with ADHD

Before Diagnosis

The worst part was not knowing I had ADHD — and hating myself for feeling broken while everyone else seemed fine.

I couldn’t understand why most interactions felt foggy. Why I struggled to remember simple tasks or conversations I just had. It felt like a handicap of the mind.

You feel compassion for those who live with visible disabilities, and yet you can’t imagine living like that. But when your disability is invisible — and your body is “healthy,” your genetics “good,” your appearance “normal” — the failure feels like a personal defect. A disappointment. Someone you wish you weren’t.

Every day was exhausting. Every day I struggled. Every day was more proof that I was inadequate and incapable, while everyone around me seemed to be handed the missing pieces they needed to feel whole — confidence, competence, connection.

Knowing that my brain worked differently filled me with dread every time I had to speak to someone.

“They’re going to see how empty I am. How broken I am.”

When nearly every interaction makes you feel foolish, you start avoiding them. The conversations get fewer. The people get more distant. And then the thoughts kick in:

“Everyone hates me.”

“No one likes me.”

“I’m weird. I’m broken.”

So the next conversation becomes high-stakes. You tell yourself this one has to go well. But the nerves kick in. Maybe I mix up facts. Maybe I stutter. Maybe I forget what I was saying halfway through the sentence.

And once again, I “fail.”

Each interaction became confirmation that I was defective — and that people were right to keep their distance. My confidence shattered. My mental health deteriorated. I began to fear speaking at all. Social anxiety took over. I isolated myself.

One of the hardest things I’ve ever done in my life was to keep walking into spaces where I felt humiliated — workplaces, social circles, family gatherings — knowing I would likely screw up again. But I kept going. I kept trying. And I kept being hurt.

I was bullied. I was mocked for being “weird,” “awkward,” for “never relaxing.”

People would joke:

“Why don’t you open up?”

“She’s like a cardboard cutout.”

I knew exposure therapy was supposed to help, but in a toxic environment, it only deepened the fear. The anxiety. The damage. Still, I kept showing up.

My family knew what I was going through and told me I had incredible inner strength. That even walking into those rooms was bravery.

Wearing a wig while doing it? Another kind of bravery altogether.

Wigs are… complicated. You get bad ones, okay ones, and maybe a decent one. I’ve yet to find one that looks real. They’re uncomfortable, itchy, and frustrating.

(But that’s a whole separate blog post.)

The worst part of all of it? Suppression. Bottling up emotions became a survival tactic. I had to stay on guard constantly — hide the ADHD, hide the fear, hide everything. Over time, I wasn’t just hiding the “defective” parts. I was hiding me.

And sometimes, those suppressed emotions would start to bubble up — and I’d be terrified to let them out.

What if I lose control? What if I do something I can’t take back? What if I push everyone away and end up alone forever?

So I kept the bottle sealed. I only let out enough to catch my breath… but never enough to heal.

The Vicious Cycle

It’s a vicious cycle. One that’s incredibly hard to break.

The people you surround yourself with can either help you climb out of it — or drag you deeper in.

(In another post, I’ll share stories of the people who played both roles.)

But the truth is something I’ve heard time and time again:

No one can save you but you.

And the moment you decide to change your life — for your good — everything begins to shift.

After Diagnosis

ADHD feels like you’re being pulled in ten directions at once.

Your brain is buzzing constantly. Everything feels urgent. Everything needs to be done now — all at the same time.

So you bounce from one task to another without finishing anything. You interrupt one activity to start a new one. You forget the first thing while trying to remember the third. And because you’re so afraid of forgetting something else, you just keep starting and abandoning.

It’s exhausting. No wonder we feel confused and foggy all the time.

This isn’t laziness. It’s not a character flaw. It’s neurology.

And knowing that? Understanding that my brain just works differently?

It changed everything.

It gave me permission to stop beating myself up. It gave me hope.

It gave me back me.

My brain is not broken. And neither is yours.

We are not defective. We are not failures.

We are healing.

Thank you for reading.

For the healing hearts.

Love,

Jenna

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