My Story

What is it like living with cerebral palsy?
I cannot answer that question, because for 46 years I never knew that is what I had. It was in March 2009 that I was finally diagnosed with cerebral palsy. I was born the second of premature twins.

My Cerebral Palsy Story

Finding My Voice

“Every day I learn a little more about myself – not by what I overcome, but by who I become in the process. Cerebral Palsy started as part of my story, but it doesn't define me. I live, I grow, and I write – because finally, my voice matters.”

– Ilana Estelle

About Me

I am Ilana Estelle – the writer and creator of The CP Diary – a reflective journal focused on emotional health, mental clarity, and conscious living.

I write so that I can make sense of a world that feels mostly noisy, divided, and difficult to understand and so that I may stay engaged. 

This isn't a space for easy answers. It's a space for careful thought, curiosity, and responsibility – to myself and to my readers.

I live with cerebral palsy, but that is only one part of my story. For much of my life, I lived with questions – about myself, how my body worked, how my emotions worked and the way I got to experience the world. Understanding came later, in the form of a cerebral palsy and autism diagnosis and with it – a different way of seeing myself and slowly my past. 

There are parts of life that I haven't been able to neatly explain, only lived and slowly understood. For a long time, I carried many of those parts quietly, to myself.

Writing became the way I began to notice, ask and to listen to myself. 

Today, The CP Diary is a space for reflection – not just mine, but yours too.

I write from exploring uncertainty, lived experiences, resilience, and the ongoing process of becoming more aware.

Each post is written with honesty and care – sometimes searching, sometimes bringing clarity, but always grounded in the need to understand.

Why I Write

I started The CP Diary more than 16 years ago as a way of making sense of my life and health with something I didn't know I had. Over time, it has grown to include reflections on health and wellbeing, current affairs, society and the wider issues that shape our everyday lives.

At its heart, my blog is about asking questions, sharing experiences and encouraging thoughtful discussion. If something I've written makes you think differently, feel less alone ,or see an issue from another perspective, then I am happy it has achieved its purpose.

My Writing

I write to understand, not to sound clever. I write for 'mental health.' This is me thinking out loud: honestly, imperfectly, and in real time.

My writing is a way of asking difficult questions, staying engaged, and making sense of my life, and a complex world with care, integrity and curiosity. I've always been curious. 

These posts are not performances or declarations of certainty. They are reflections, shaped by lived experiences, mental health awareness, learning, and ongoing self-awareness.

I am not a medical practitioner, and I do not offer diagnosis or clinical treatment. What I share through The CP Diary are reflections, insight, and awareness – informed by both my experiences and education – intended to encourage understanding, self-compassion, and conscious living.

At its heart, The CP Diary is a place to pause, to reflect, and to feel less alone. It is for anyone who feels deeply, for anyone is navigating their own journey – whether that includes mental health challenges, disability, long-term conditions, or simply the weight of being human.

My story is not a story of limitation. It is a story of awareness, resilience, but mostly of becoming 'me' with all of my imperfections. 

My Approach to Writing

The CP Diary isn't a record of finished thoughts. Those thoughts are on-going. It's a space where my thoughts happen.

My writing doesn't come after thinking – it lives inside it.

Each entry is composed while my mind is curious, still moving, still questioning, still rearranging itself.

With autism, I write to understand, for me to be able to see things more clearly, not to sound clever. This is me thinking out loud – honestly, imperfectly, and in real time.

The CP Diary is a space for asking difficult questions, staying engaged, and trying to make sense of the world without feeling overwhelmed – with care, integrity and curiosity.

If you're looking for answers you may find them here. What you may also identify with, is a mind in progress – often reflective – and with autism – mostly always overwhelmed.   

Why Read My Articles
  • Honest reflections on mental health and emotional wellbeing
  • A distinctive voice shaped by sincerity, in good faith, and lived experience
  • Gentle, relatable writing for healing, connection, and thoughtful living
  • Encouraging insights on growth, resilience, and self-awareness
  • Calm perspectives on life's challenges and emotional wellbeing
  • A supportive space that values emotional truth, vulnerability and strength
  • Thoughtful discussions that remind readers they're not alone

The CP Diary offers more than articles: it provides a reflective space for reassurance, clarity, and emotional connection.

A Note About The CP Diary

We spend our lives trying to understand who we are and why we experience the world the way we do. For me, that journey led to the late discovery of cerebral palsy and later, autism – answers that brought clarity of a life lived without – and a new way of seeing my life.

The CP Diary is where I get to explore those experiences. It's a place for reflection, self-discovery, resilience, and honest conversations about the complexities of experiences. Through my writing, I share what I have learned, about finding meaning in our experiences, acceptance, and growth.

So, whether you are here looking for understanding, support, or simply a different perspective, I'm glad you have found your way here.

Welcome to The CP Diary

The CP Diary

What’s shared here isn’t meant to convince, but simply to sit alongside anyone who finds themselves questioning, or simply looking for quiet understanding.

Some stories are abstract, some more personal – all written with care, and offered without expectation.

If you’re here, thank you, you’re very welcome to stay and read. And also to leave what isn’t yours to carry.

Writing creates space – to pause, to reflect, and to make sense of the things we don’t yet understand, things that life places in our path. It allows honesty to surface gently, without pressure or expectation.

The CP Diary is a space for open conversation around mental health, chronic illness and healing. The CP Diary exists to give voice to stories that are often ignored, softened, or silenced.

The writing doesn’t come after understanding – it lives inside it. Each entry is written while the author's mind is still questioning, still moving, still rearranging itself.

We all have moments of clarity, but not every question arrives with a conclusion. Sometimes understanding is something the reader has to discover.

What you’ll find here is a mind in progress – reflective, questioning, always curious. Writing grounded in integrity, guided by a strong moral compass.

And that matters.

Over the years the focus has shifted – now it's more about learning how to carry things differently.

Through time we come to work things out, to our own understanding – an understanding that not everything can be resolved, but some experiences still ask to be recognised. 

Perhaps part of what comes next is allowing these reflections to exist outside of me, so they don’t have to be held alone.

Thanks for being here and for reading.

The CP Diary Articles

Not every article on The CP Diary is autobiographical. I also write about universal themes, shared struggles, and the wider human experience.

Where You Can Find My Selective Works

My writing is primarily published through The CP Diary. The socials I am most active on are: X, Facebook, Tumblr, Medium and Goodreads, where I share articles, relating to The CP Diary.

I am a member of the Society of Authors, the UK's professional body for writers.

Background and Learning

Alongside my lived experience, I draw on formal study in counselling, nutrition, stress management, and emotional wellbeing, with a focus on holistic wellbeing, self-awareness, and emotional resilience.

Diplomas and qualifications include:

Oxford College
– Diploma in Counselling
– Diploma in Diet and Nutrition (Distinction)
– Diploma in Nutritional Therapy (Distinction)

The School of Natural Health Sciences
– Diploma in Stress Management
– Diploma in Psychotherapy & Counselling
– Diploma in Advanced Nutrition
– Higher International Diploma in Nutrition

What I’ve learned through these studies helps me to make sense of emotional patterns, stress, resilience, and health and wellbeing, while my writing stays rooted in reflection, not instruction.

Love and light,
Ilana x


MY STORY


How did I feel as the child then, the adult now? I can't answer that because I didn't know then what I know now. I had no idea I was disabled. 

What I do know is those times were enormously difficult. I was an angry child living in the depths of despair. Some days I felt isolated, angry, alone and always misunderstood. Other days I was irritated, frustrated and helpless to help myself.

I first had a diagnosis of cerebral palsy at the age of two. There were concerns about my balance. When my twin began to crawl, I would fall, try to get up, then fall again. It was never something I could control.

Growing up, I felt different for all the wrong reasons. I knew there were things I struggled with, but nothing was ever explained. We didn’t talk about what was wrong, or how my symptoms presented. My issues were never brought up unless I mentioned them – and then they were quickly dismissed as if the condition didn’t exist. But it did!

I had little muscle tone from the hip to the ankle on my left side. I have a foot drop, and my left leg is ¾” shorter than my right. I have a weakened and smaller muscle tone and a paralysis on my left side that extends to my arm. 

As a child I dragged my leg and walked toe-heel. I limped and tripped when I got tired. I struggled with shoes. I wore a heel lift. Eventually I had shoes made for me.

I struggled with handwriting. I struggled with being watched. I struggled with looking at myself in the mirror because I stood lopsided. I hated that and being picked on for something I couldn't change.

For many years I didn't understand what I was dealing with – physically, mentally or emotionally. Questions weren't asked. There were no discussions and with no emotional support as a consequence, I learned to stay small and work things out for myself.

I spent my formative years being angry, but still I always knew deep down I wasn’t a bad child – I was an angry child with something I didn't know I had.

Over the years I have had to bring my symptoms and my diagnoses together. The correct diagnosis is 'Mild Cerebral Palsy Hemaperisis and Autism.' With my notes in my possession now, I understand more than I ever did.

My neurologist later explained that the part of my brain responsible for motor skills is affected. That knowledge has brought clarity, helping to explain my handwriting and some of the learning difficulties I have experienced. At 56, understanding that I am autistic has also helped me make sense of a lifetime of misunderstandings, failings and feeling different.

Not knowing gave me a false, renewed hope that tomorrow would be different. Throughout those difficult decades, I hung on to believing that tomorrow was another day and that things could change for the better.

I was wrong.

This is my story – of a disability that was brushed aside, of anger that got the better of me, of masked ignorance... and of learning to understand myself decades later.

The light: I remember subconsciously thinking I was happy being me. Perhaps the light was never the moment itself, but the certainty I carried within it.

Thanks for reading,

Ilana x

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