Falling in Pieces

When it started falling,
It left a trail of where I’d been.

No one said a word.
Maybe it was nothing.

But day after day,
It kept falling.

Too much.
Too fast.

There was no denying it,
Only proof.

Something was wrong.
I must be sick.

But I was young.
I was strong.
I felt fine.

It felt like a curse from above.
Telling me I did something wrong.
Telling me I deserved it.
Telling me I didn’t belong.

My hair isn’t mine anymore.
It belongs to someone else.

I started to fear
the touch of another person.

I miss the feeling
of fingers combing through my hair,
followed by a kiss,
and the comfort I used to know.

I miss the wind
How it once felt free.

I miss the water
How it once brought me calm.

I miss when my hair
didn’t feel like a lie.

I hate what’s become of me.
I hate this cage.

I hate the way I shrink inside.
Like I take up too much space.
Like I’m too much and never enough
All at the same time.

I grow envious
of the girl with someone
who twirls her hair.

Who tells her it’s beautiful,
how soft it feels,
how it’s part of her,
and why he loves her.

Who tucks her hair
behind her ear,
and whispers a secret
only meant for her.

All I can do
is watch from a distance,
and dream
of what it might feel like
to be her.

The Alopecia Diaries

Dear Diary,

I’m worried,  my eldest son might be growing a bald spot on his head.  I remember telling my husband how I was scared to have kids in case they get my disease.  The hardship and turmoil I went through I would never wish on anyone.

As a parent and as someone who went through it, I started asking myself,  Do I wait to take him to the doctor until I know for sure?  Do I wait to prepare the dialogue I need to tell him so I can give him the right peace of mind?  

What if the diagnosis comes back true?  Knowing that mommy wears a wig because of it and ends up having terrible anxiety over imagining if he needs to wear a wig as well. It makes me feel sick to my stomach.

I imagine the doctor coming back with a positive result and how he would react.  I can picture him looking down at the floor trying to be brave and becoming extremely quiet in front of the doctor.  

I imagine when we get home he starts to scream at me,  yell at me, curse at me, push me, hit me, hating me, hating the world, and wishing I was never his mom.  Wishing he was never born in this family.

I wouldn’t blame him.  I thought the same thing except there was no historical path to trace back to.  So there was no one I could blame.   So I ended up feeling alienated.  I started wondering if I was adopted or had a different father or worst of all, that I was the only freak of nature in the family.  That the world must hate me and perhaps I somehow deserve this.  Maybe I was a very awful person in my past life.  Which I don’t necessarily believe in past lives but sometimes when things just don’t add up properly,  you start believing in fate, destiny, god, the universe and the path that was written for you.

I can’t believe how afraid I am to make this doctor’s appointment.  I wanted this to be my battle, not something I pass onto anyone else.

If the diagnosis comes back positive, the only thing I can think of to tell him is,

“I know exactly what to do if you want to hide it.”

“I know exactly what to do if you want to leave it alone.”

“I’ll teach you how to live in this world with this and how to handle bullies.”

“I’m here as much or as little as you need. “

“I will always be here for you at any hour, on any day, no matter what.  I’ll  help you get through every difficult moment.”

The thing that scares me about this disease is how completely unpredictable it is.  It  can be ok for a while then out of nowhere, boom, a bunch of hair falls out, and you have zero reason why.

You can be happy and positive – it doesn’t make a difference.  The disease can still take an aggressive turn that doesn’t make sense.

Stress of course does play a factor as well as poor diet and poor sleep.  

But I don’t know what to do.  I’m freaking out.  I hate myself for passing on this awful disease when I could have decided not to.  I could have decided not to have kids.

I’ll understand if he hates me forever.  If I’m the blame, the source, the enemy.

I am ready to take his blows, his hate, his anger, his frustration.  I’ll take it all.  I’ll be waiting to hear his story.  I’ll be waiting for him to disown me and never want anything to do with me.

But, I’ll love him forever, always and to infinity.  

With everything that I am and more than he’ll ever know in this entire lifetime.

As always diary, thank you for listening,

Love,

Jenna 

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. 🫶🏻

Hair Isn’t Just Hair: Living with Alopecia, Navigating ADHD, and Finding My Identity

Alopecia is a disease—an autoimmune condition where the immune system mistakenly attacks hair follicles, treating them as a threat. There are three main types:

  • Alopecia Areata – Patchy baldness on the scalp or other parts of the body
  • Alopecia Totalis – Total baldness of the scalp
  • Alopecia Universalis – Total hair loss across the entire body

I have Alopecia Areata.

It started when I was just three years old — one small bald patch. My parents took me to the doctor, and the advice was simply to wait and see. Thankfully, my hair grew back. Everyone forgot about it… including me.

Eventually, I went on to have thick, beautiful hair — so thick my mom could only twist an elastic twice for a ponytail.

Losing My Hair, Losing My Identity

Then something changed. My grandpa passed away when I was around eight, and it was the first time I truly experienced grief. Shortly after, I started losing hair again — only this time, it was much more noticeable.

Another doctor visit followed. This time, I received a diagnosis: Alopecia. The doctor pointed out “exclamation hairs”—thin at the base, thicker at the tip. They’re a telltale sign that hair loss is progressing.

There’s a gut-wrenching feeling when you step into the shower and watch chunks of hair fall out. Some days are better. Others, worse.

I kept asking: Why me? No one else in my family had this. I was angry. Was this a test? A punishment?

I imagined life as a lottery. Some win health, beauty, and fortune. Others, like me, get dealt invisible pain and visible difference.

I never wanted to complain to anyone else. Instead, I just wished I could pretend I was like everyone else.

Hiding became my shield. However, the wind terrified me most—what if it blew just right and exposed my secret to the world?

Sometimes I’d trace the bald patches with my fingers, as if the shapes could explain why they existed. Strange circles. Mirrored patterns. Like brain scans. Or inkblot tests used to decode your mind.

Eventually, I gave up asking doctors. The treatments failed. Hope drifted further away until it disappeared completely. I surrendered.

But surrender didn’t bring peace. Instead, it felt like paralysis. I had accepted a version of myself I never wanted to be. I was no longer fighting for answers—I was simply surviving without them.

Still, those cards I was dealt led me here. They forced me to find strength I didn’t know existed. I learned what it means to crawl upward from rock bottom.

What Alopecia Took Away From Me

Alopecia took away pieces of my femininity. The intimacy of someone running their fingers through my hair. The simple, sensual feeling of wind in my hair, water rinsing over my scalp. All of those moments were taken from me.

Sometimes, I long for those cinematic gestures. The ones where someone tucks a strand of hair behind your ear. Or gently pulls it in a passionate moment. Unless there’s a cure, I may never know what that feels like.

Having someone touch my wig is something I deeply avoid. It’s not what I want them to feel.

Above all, I miss freedom. The freedom of no limitations and no fear. That’s the hardest part.

What It Feels Like to Wear a Wig

Wearing a wig feels like putting on a tight, itchy net. Even the finest lace itches. I try not to think about whose hair it once was. Instead, I pretend it’s mine.

Most days, it feels stifling—too tight, too hot. Sometimes the glue doesn’t hold. Or the style I want isn’t possible. It can feel like a cage I can’t escape.

I’ve lost count of how many times I’ve wanted to rip it off and throw it across the room in frustration.

But I know I can’t. I know I have to wear it—because it’s the only thing that helps me feel okay in this world.

The Strength I Needed to Live With Alopecia

Denial was my biggest coping strategy. I told myself the wig was my real hair. I told others the same. As a result, I denied myself space, voice, boundaries—even feelings.

It takes radical strength to carry this every day and pretend everything’s fine. You endure silently, without ever expressing the chaos inside.

Over time, I’ve changed. I’ve rebuilt. The girl I was is almost unrecognizable. Looking at old photos, I see the fear in my eyes. The tension in my smile.

Discovering I Also Have ADHD

Therapy helped me uncover more of myself. I wasn’t just living with alopecia—I was also living with undiagnosed ADHD.

There were signs. I would forget what I was saying mid-sentence. I lost things constantly. Focusing became nearly impossible. As a result, I blamed myself and felt defective—like I was broken.

What ADHD Feels Like for Me

Then I found others with ADHD online. I laughed at their reels, watching the humor unfold—and in those moments, I saw pieces of myself reflected back.

For the first time, I realized: maybe I wasn’t broken. Maybe I was simply different. That discovery changed everything.

What I’ve Learned About Being Neurodivergent

Being neurodivergent doesn’t mean you’re less intelligent. It means your brain processes things differently. Some of us learn visually. Others need movement. Neurodivergence works much the same way.

Now, when my brain blanks or I freeze, I have tools. I understand what’s happening—and I know I’m not alone anymore.

The Latest Treatment for Alopecia: Litfulo

There’s no cure yet. However, in 2023, Pfizer released Litfulo, the first FDA-approved treatment for Alopecia Areata. It’s a JAK inhibitor, designed to regulate immune response.

While it’s promising, Litfulo carries serious side effects:

  • Lowered immune function
  • Risk of serious infections
  • Blood clots
  • Elevated liver enzymes
  • Potential long-term cancer risks

After reviewing these risks with my doctor, I’ve chosen to wait. For now, it’s not the right path for me.

This is my personal choice—not medical advice. Please consult your doctor for your own situation.

In the past, I tried creams and injections. They only brought temporary results. I still remember my mom gently applying numbing cream before those appointments. Her love softened the pain.

She was an incredible mother. I’m endlessly grateful for everything she did.

Until there’s a safe cure, we live with hair loss together.

With love,

Jenna

🔗 Learn more about Litfulo on Pfizer’s site

✨ Are you navigating alopecia or ADHD too? Let’s talk about it—drop a comment below or share this post with someone who needs support. We’re in this together.

🖤 Welcome to Wig Girl Interrupted

Hi, I’m Jenna — and I’m finally ready to stop hiding.

Starting this blog feels both exciting and terrifying. I’ve never done anything like this before — no personal site, no blog posts, nothing that asked me to be this visible. But after everything I’ve been through — from childhood hair loss to years of self-erasure — I know this step matters.

Sometimes the scariest things are the most important.

✨ Why I’m Here

For most of my life, I struggled to understand what was wrong with me.

I lost my hair as a child and spent years covering it with wigs, trying to blend in. I froze in conversations, avoided mirrors, and shrank myself in relationships that fed on my silence.

I was anxious. Confused. Emotionally exhausted. I didn’t have the words to explain what I was feeling — or why I felt like I was constantly fighting myself.

Then at 39, I was finally diagnosed with ADHD. That moment didn’t fix everything, but it helped me understand myself for the first time. It explained the chaos, the forgetfulness, the emotional flooding, the years of masking.

But even more than that — it helped me begin coming back to myself.

🕊 What “Wig Girl Interrupted” Means

This blog is my space to speak what was once unspoken — about identity, trauma, healing, and transformation.

The name Wig Girl Interrupted represents the pause I’ve lived in for far too long.

Interrupted by alopecia. By toxic relationships. By silence.

Now, I’m writing my way out of that interruption.

Here, I’ll talk about:

  • Life with alopecia and wigs
  • Living with ADHD (and the shame that comes with it)
  • Healing from emotional abuse
  • Rebuilding identity after years of people-pleasing
  • Finding my voice — even when it shakes

💛 If You’re Here, Thank You

If you’ve ever felt like your brain, body, or heart didn’t work the way they were “supposed” to…

If you’ve lost yourself in a relationship, a diagnosis, or the pressure to be everything for everyone…

If you’ve felt interrupted — by life, grief, shame, or silence — this blog is for you.

I don’t have all the answers. But I promise to be real.

If you’re new here, I recommend you Start Here.

Thank you for being here. I can’t wait to grow together.

With love,

Jenna

🪞 Healing is easier when we don’t do it alone. Pass this along to someone who needs to feel seen.

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