Featured in the local & national press
Coverage of my journey living with hidden disabilities and my advocacy work.
Disability advocate, published author, public speaker and content creator on a mission to make hidden disabilities seen, heard and valued.

I've spent my whole life living with multiple rare conditions. They're a big part of my story, but they don't define my limits, they shape my purpose.

I've never really known life without hospitals, operations and the fear of uncertainty. But every one of these experiences has made me more resilient, and helped me realise that being different is my strength. That's what drives me to advocate, write and speak, so others who feel different know they are never alone.
Diagnosed from birth with 22q11.2 syndrome and the heart defect Tetralogy of Fallot.
Endured my first open-heart surgery at just one year old, and another later on.
Learning to find my way through education while partially deaf, partially sighted and living with a learning disability.
Building the confidence and skills to live life on my own terms.
A milestone that opened up new freedom and independence.
Publishing Between Heartbeats, a novel for anyone who has ever felt different.
Turning my experiences into a mission to raise awareness of hidden disabilities.
My debut novel follows teenager Aria Chapple, who undergoes major heart surgery and, while fighting for her life, creates an entire world inside her mind, five chambers where she faces the struggles of growing up.

Drawing on my own life with a congenital heart condition and multiple rare diagnoses, Between Heartbeats is a story about courage, imagination and finding strength in what makes you different.
Buy Now on AmazonThis book is for anyone who feels different and doesn't see themselves as perfect.
A moving, imaginative story that stays with you long after the final page.
Beautifully written and full of heart, it captures resilience like nothing else.
I speak openly and warmly about life with hidden disabilities, sharing my story to help audiences understand, include and champion people who are different.

A selection of interviews, articles and appearances where I've shared my story.

My mum said I "never cease to amaze" her, read the full BBC feature on my life and my novel.
Read the articleCoverage of my journey living with hidden disabilities and my advocacy work.
Talking openly about 22Q, heart conditions and finding strength in difference.
Raising awareness of hidden disabilities with radio audiences.
Bite-sized explainers to help you understand, include and support people living with hidden disabilities.
Many disabilities can't be seen at a glance. Someone may look 'fine' while managing pain, fatigue, sensory differences or a serious health condition. Believing people and offering understanding matters.
Hidden (or invisible) disabilities include conditions affecting hearing, sight, mobility, energy, learning and mental health that aren't immediately obvious. They are just as real and valid as visible ones.
22q11.2 deletion syndrome (also called DiGeorge syndrome) is a condition caused by a missing piece of chromosome 22. It can affect the heart, immune system, learning, speech and more, and looks different for everyone.
Congenital heart conditions like Tetralogy of Fallot are present from birth and can mean surgeries, monitoring and adapting daily life, while still living fully and pursuing big dreams.
Small adjustments, flexible working, clear communication and inclusive design help disabled people thrive at work. Accessibility benefits everyone, not just those who ask for it.
Words matter. Ask people how they'd like to be described, focus on the person, and avoid outdated or pitying terms. Respectful language helps everyone feel seen and valued.
“I'm on a mission to educate the world about hidden disabilities, empower people to embrace who they are, and create a future where everyone feels seen, heard and valued.”
22Q is one of the most common syndromes you've probably never heard of. Raising awareness helps families feel less alone.
22q11.2 deletion syndrome, also known as DiGeorge syndrome, is caused by a small missing piece of chromosome 22. It can affect the heart, immune system, speech, learning and physical development, and affects everyone differently.

My Tetralogy of Fallot in particular has shaped every part of who I am. I've never known life without hospitals and uncertainty, but 22Q has taught me resilience, and I want every family facing it to know there is hope, strength and a whole community behind them.
I bring my story to schools, workplaces, charities and community groups — in person or online. Every talk is warm, honest and shaped around your audience.
Assemblies and workshops on disability, difference and resilience.
Inclusion, accessibility and hidden-disability awareness sessions.
Lived-experience talks for support groups and community events.
Flexible formats to suit your audience, wherever you are.
To book or ask a question, email:
zoemcastle@hotmail.co.ukOpens a ready-to-send enquiry email
Whether you'd like to book me to speak, chat about my book, or invite me for an interview, I'd love to hear from you.