About Me
My Name is Josh Wright.
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A 28-year-old creator, designer, and the founder of Seeking Serenity Apparel, a clothing brand dedicated
to raising awareness around epilepsy and mental health.
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For over a decade now, I’ve lived with epilepsy. I was diagnosed at the age of 16, and since then, my life has
been a journey filled with highs, lows, uncertainty, and ultimately; growth.
Living with epilepsy isn’t easy. It has impacted every part of my life: my mental health, my confidence, my independence, and at times, my sense of hope. There were moments where I felt lost in the darkness, unsure of who I was or how I could find peace within myself.
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But over the years, something changed.
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I realised I wasn’t alone.
That others out there were struggling too; fighting invisible battles with epilepsy, anxiety, depression, trauma, or simply trying to keep their heads above water in a world that doesn’t always understand. That realisation sparked something inside me. I wanted to turn my struggle into something meaningful; not just for myself, but for everyone who’s ever felt isolated, misunderstood, or invisible.
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That’s when Seeking Serenity Apparel was born.
Why I Started This Brand
Seeking Serenity isn’t just clothing; it’s a message, a movement, and a symbol of strength.
Every design is inspired by real experiences; not just mine, but those shared with me by people navigating mental health challenges and neurological conditions like epilepsy.
I wanted to create something that could speak without saying a word; something that could start conversations, raise awareness, and give people the confidence to express what they’ve been through.
Clothing is powerful. It’s identity. It’s expression. It’s community.
I believe awareness saves lives; and that design can become a voice for those who sometimes struggle to find their own.
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My Mission
To spread awareness. To inspire healing and conversation.
To build a community rooted in truth and strength.
To show that even through darkness; there is always a path to light.
If you’re reading this and you’re struggling; please know this; you are not alone. Your story matters.
Your voice deserves to be heard.
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Let’s End the Stigma Together
Mental health isn’t a trend; it’s a reality for millions.
Epilepsy; though often hidden; affects around 1 in 100 people. Yet it remains deeply misunderstood.
By wearing Seeking Serenity Apparel, you’re not just wearing clothing; you’re starting a conversation, spreading awareness, and standing beside those who may be silently struggling.​
Founder Q&A
How were you diagnosed, and did it surprise you?
I was diagnosed after experiencing seizures that completely shook my world.
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Before I understood what was happening, my mind searched for explanations; and at one point, I genuinely thought I might have been possessed!
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That fear came from not knowing; from feeling completely out of control.
Strangely, hearing the word epilepsy gave me more relief than fear; because at least I finally knew what I was facing.
It was still a shock; but it gave me a starting point. From that moment, I knew life would be different; but I also knew I had to find the strength to keep going.
What knowledge of epilepsy did you have before your diagnosis?
Honestly; almost none.
What I thought I knew came from stereotypes; like flashing light warnings before films. I believed epilepsy was only about visible seizures triggered by lights.I had no idea how deeply it could affect your mind, emotions, confidence, and daily life.
Now I understand just how misunderstood it is.
Around 1 in 100 people live with epilepsy; yet many still think it’s “just flashing lights.”
Those are the people I want to reach most; because awareness begins where misunderstanding lives.
How does it affect your everyday life?
Epilepsy is something I carry with me every single day.
It affects how I plan; how I think; and sometimes how I feel about myself.
There’s unpredictability. There’s fear. And there are moments when it feels heavy.
Some days are harder than others; but it has forced me to grow.
It has made me stronger and more self-aware than I ever expected to be. Even on uncertain days; I keep moving forward.
What do people often misunderstand about epilepsy?
People often think epilepsy is only what they can see; someone collapsing or having a visible seizure.
But much of epilepsy is invisible. It can affect memory, focus, emotions, and mental wellbeing.
There is also a painful misunderstanding around opportunity.
Many people with epilepsy face discrimination; especially in employment. Sometimes the moment someone sees the word epilepsy; they see risk instead of resilience.
That judgement is built on fear; not truth. People with epilepsy are just as capable, determined, and valuable as anyone else.
What’s one thing you wish people knew?
I want people to move beyond stereotypes and truly see the person behind the condition.
Epilepsy does not take away intelligence, ambition, strength, or potential. It does not define someone’s character, their ability, or their future. A diagnosis should never determine someone’s worth or limit what they can achieve.
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What often holds people back is not the condition itself; but the misunderstanding surrounding it.
Epilepsy is more common than many realise; around 1 in 100 people live with it. Nearly 70 percent of those individuals have their seizures fully controlled; sometimes going years without one. Yet the word epilepsy still triggers fear, assumption, and stigma. That reaction can lead to judgement, discrimination, and missed opportunities; particularly in workplaces and everyday life.
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The condition itself is not weakness. The diagnosis is not a limitation, and the person is never defined by it.
No one with epilepsy is broken or should feel invisible.
No one should be judged, and no one should lose opportunity because of a diagnosis they did not choose.
The more we understand; the less we fear.
And the less we fear; the more inclusive the world becomes.