Caroline Prout
hypnotherapy & coaching
Thank you for agreeing to speak at the East of England Assistants Conference. We’re really excited to have you involved. To help us introduce you properly to the community, we’d love you to share a little more about yourself.
This form helps us build your speaker profile page, which will be shared with attendees before and after the event. It’s also something we’ll use across our website, social channels and conference materials so people can learn more about the expertise and experience you bring.
We encourage you to include as much detail as you’re comfortable sharing. Your journey, the work you do, the problems you help people solve, and what led you into your field are often just as interesting and valuable as the headline achievements.
Our audience is made up of assistants at all stages of their careers from people just starting out to highly experienced professionals running their own businesses. The more context you can provide about your experience, your perspective and your approach, the more useful and inspiring it will be for them.
Caroline’s Story
From Burnout to Balance
Living and Recovering from Chronic Fatigue Syndrome
For many years I lived with Chronic Fatigue Syndrome—often called M.E.—without fully understanding what was happening to me. It started one winter, after a virus I simply never seemed to shake off. One day I was running, swimming, doing yoga, working hard and socialising freely; the next I was struggling to put one foot in front of the other or even string a sentence together. It was as if the version of myself everyone knew had vanished overnight, and no one could see why I was suddenly so different.
Talking about it felt almost impossible. When I tried to explain, “I have CFS and I’m really struggling,” well‑meaning friends would describe being tired after a late night or a busy week. They’d mention needing a lie‑in or a glass of wine, as if energy were purely a matter of rest and leisure. But CFS isn’t ordinary tiredness; it’s like having a mobile phone with a dodgy battery that never holds a full charge, randomly dying from 90% down to 2% with no warning. Some days a short text could drain me; others, even a simple conversation left me needing to cancel everything and retreat.
That lack of energy reached into every corner of my life. My thinking fogged over; simple tasks like matching lids to pots or remembering basic words became huge efforts. I felt slow, clumsy, stupid—like I was failing at things that had once been effortless. To save what little energy I had, I stopped saying yes to social plans, hobbies, even things I loved. I carried emergency snacks everywhere, always on the lookout for a chance to “recharge,” but I still crashed in meetings, at social gatherings, in supermarkets. Slowly, my world shrank and loneliness settled in, underlined by the fear that no one really understood me.
Behind the exhaustion lay years of stress, anxiety and a battered adrenal system. CFS isn’t just “not getting enough sleep”; it’s an outcome of the body’s stress‑management machinery burning out. Constant cortisol production, repeated fight‑or‑flight responses, and unresolved trauma can leave the adrenal system weak, so it struggles to regulate hormones, blood sugar, immune responses and even tolerate everyday foods or stimuli. In that state, my system became hypersensitive: caffeine, sugar, late nights, gluten, dairy, strong smells, even a “normal” week of work could tip me into a crash that left me bed‑bound for days.
Recovery didn’t look like a single dramatic cure. Instead, it became a continuous process of recalibration. I learned to reduce “toxins” my body struggled with—substances others might tolerate easily—so my adrenal system had less to do. Regular home‑cooked food, gentle movement like yoga, fresh air, consistent sleep and emotional regulation all helped my body drift back toward balance. On good‑week days, a small indulgence might be manageable; after a busy, stressful week, even a glass of wine could trigger a crash. But over time the crashes became shorter and less severe, and I grew confident in my ability to steady myself.
Now, as a clinical hypnotherapist, I use my own experience to help others who feel as isolated and confused as I once did. I help them re‑energise, reconnect with who they are beyond their symptoms, and design a life that supports their nervous‑system health instead of exhausting it. Recovery from CFS is possible, but it’s less about returning to an old “normal” and more about building a new way of living—one that honours the mind–body link, respects the adrenal system, and allows for both survival and, eventually, thriving.
Dyspraxia and Difference
Navigating Life with a Brilliantly Different Brain
Dyspraxia has always been part of who I am, even though most people wouldn’t guess it from the outside. It’s a neurological difference that doesn’t affect my intelligence but quietly reshapes how I move, think and live. My brain processes information more slowly, with some messages arriving late or only half‑formed, as if the motor neurons never quite connected properly. I often feel out of sync with the world, a few degrees off, like my body and brain are using different languages and the translator is always a little drunk.
This shows up in the smallest moments. I’m covered in bruises because I don’t quite register where my body is in space, even in familiar places at home. Simple tasks like tying shoelaces, brushing my teeth or putting on makeup are complex puzzles. I keep my hair up because drying it in front of a mirror requires me to co‑ordinate two hands, two tools and a mirrored image all at once—my brain just gives up. Escalators are daily drama: my brain is late to tell me when to step, and getting off feels less like landing and more like a controlled crash.
Left and right are still a mystery to me - my brain won’t compute it. Telling the time feels like starting from scratch every time, so travelling is a constant low‑level panic. I rely on post‑it notes, timers and someone else double‑checking my schedule and still sometimes get it wrong. Organisation is a survival skill, not a natural talent: I keep my planner, highlighters and colour‑coded systems visible, while underneath every room hides a drawer of chaos.
Dyspraxia made school exhausting. In a noisy coffee shop, I can’t filter out background noise; everyone’s conversation feels the same volume. I can’t reread a factual book without coloured highlighters to anchor my eyes; without them, the words slip and slide off the page. Learning to drive and swim came in my thirties, far later than everyone else, because my brain needed everything broken down differently in a way my out‑of‑sync brain could follow.
The constant extra effort leads to fatigue, and the constant not‑quite‑getting‑it feeds anxiety. There’s a general hum of unease in the background, not tied to any one thing. It makes communication harder too: I sometimes use the wrong word, talk over people, or struggle to catch the timing of a conversation.
But dyspraxia also gives me strengths. I’m highly creative in patterns and rhythms, not in the traditional “draw realistic pictures” way, which is why I love painting mandalas and collage art. I find novel ways around problems and tend to see the world from a slightly different angle.
Now, I see my dyspraxia as part of what makes me, me. I’ve learned to work with it rather than against it and have let go of needing to do everything the “normal” way. Fractions? My phone has a calculator. Driving somewhere? Sat‑navs are a gift. What I want others to take away is this: have patience with difference. We’re all wired differently, and it’s in those differences that the world becomes richer, kinder and more interesting.
If this story resonates with you make sure you book a seat at this year’s conference and hear from Caroline as she speaks on our well being panel.