Hydrocephalus

Hydrocephalus — commonly called “water on the brain” — is a condition in which cerebrospinal fluid builds up inside the brain’s ventricles, causing pressure that can affect brain development, movement, cognition and behaviour. It affects around 1 in every 500 children, making it one of the most common serious neurological conditions in childhood.

This section of Brain Care Path covers everything families need to understand about hydrocephalus: what causes it, how it is diagnosed, what a VP shunt or endoscopic third ventriculostomy (ETV) involves, and what life looks like after treatment. You will find articles written in plain language, medically reviewed by practising neurologists, covering topics from early warning signs in babies and toddlers to shunt revision surgery, long-term cognitive effects, school support, and daily life management.

Whether your child has just been diagnosed or has been living with hydrocephalus for years, the articles here are written by a parent who has walked this road — and reviewed by specialists who understand the clinical picture. Use the articles below to find answers, ask better questions at your next appointment, and feel less alone in the journey.

South Asian father holding young toddler son closely in children's hospital, love and determination
Hydrocephalus

Hydrocephalus and Seizures: Why They Happen and How Families Manage Both

When every moment matters — navigating seizures and hydrocephalus together. The first seizure happened three weeks after my son’s shunt surgery. I was in the room. He was lying on the bed and suddenly something changed — a stiffness, a tremor, his eyes rolling. It lasted less than a minute. It felt like an hour. We were back in hospital that same night. By the next morning, there was a second diagnosis to learn: epilepsy, secondary to the hydrocephalus. Two conditions. Two medications to understand. Two separate sets of warning signs to memorise. If this is where you are — managing both — this article is for you.

South Asian father sitting at his young son's hospital bedside at night, soft lamp light, love and exhaustion
Hydrocephalus

Our 28 Days: How Hydrocephalus Went Undiagnosed for Nearly a Month

Twenty-eight days before a diagnosis that would change everything. The fever started, and we gave him paracetamol. That is always how it starts, is it not. Something manageable. Something every parent has done a hundred times. You check the temperature, you give the dose, you watch through the night. Two or three days later, the fever had not broken — it had climbed. We took him to the doctor. Throat infection, he said. He prescribed antibiotics. We went home and began the course, certain that within a few days we would be through the worst of it. The fever did not go down. We went back. The doctor increased the strength of the antibiotics.

Parent reading about hydrocephalus diagnosis with young child
Hydrocephalus

Early Warning Signs of Hydrocephalus Doctors Sometimes Miss

For 28 days, my son had hydrocephalus and nobody caught it. He was seen by multiple doctors, admitted to hospital, treated for tuberculosis — and the real cause of his deterioration went undetected for nearly a month. He was three and a half years old. I am not writing this to criticise doctors. I am writing it because I wish someone had written it for me. Hydrocephalus — the buildup of cerebrospinal fluid inside the brain — is a serious neurological condition. It is also one that is frequently missed, delayed in diagnosis, or misattributed to other causes. Understanding why it gets missed — and knowing what signs to push for — could save your child months of suffering.

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