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Child · 1 to 12 years

Children with inflammatory bowel disease

Nutrition support for children with Crohn's or ulcerative colitis. Exclusive enteral nutrition, dietary triggers, and maintaining growth through flares.

Read more about me
Best forChildren 1 to 12
FormatOnline · 60 minutes
IncludesWritten plan
Fee£90 new patient
Child enjoying a healthy meal
Colourful fresh food for children
Parent and child preparing food together
Baby exploring food during weaning
Fresh fruit and vegetables
Family mealtime with healthy food
Child with a balanced plate
Healthy ingredients for children's meals
Baby-led weaning with finger foods
Mother feeding infant
Happy family eating together
Child enjoying a healthy meal
Colourful fresh food for children
Parent and child preparing food together
Baby exploring food during weaning
Fresh fruit and vegetables
Family mealtime with healthy food
Child with a balanced plate
Healthy ingredients for children's meals
Baby-led weaning with finger foods
Mother feeding infant
Happy family eating together

Why nutrition is treatment, not just support

IBD in children isn't just a gut condition. It affects growth, puberty timing, bone health, energy levels, and quality of life. Nutrition is part of the treatment itself - not a nice-to-have alongside medication, but a core component of managing the disease.

For newly diagnosed Crohn's disease in children, exclusive enteral nutrition (EEN) is recommended by NICE as first-line treatment to induce remission. That means a complete liquid feed as the only source of nutrition for six to eight weeks. Research suggests it works in around 80% of children with mild to moderate Crohn's, and evidence indicates it can be as effective as steroids, and without the side effects. It also supports catch-up growth, which steroids actively work against.

EEN is not easy - six weeks of no food is a big ask, especially for a child - but with proper support and planning, many families manage it, and the results can be very encouraging. This is exactly the kind of work where specialist dietetic input can make a real difference.

Managing nutrition during flares

During active flares, the priorities shift. Maintaining adequate intake when a child feels unwell, nauseous, or in pain is challenging. Dietary priorities shift — it's a time for pragmatism, and the specific approach depends on the child's symptoms and disease activity. This is exactly the kind of thing a consultation covers.

Some children lose weight rapidly during flares, and catching up afterward is important. I work out calorie and protein targets for recovery, plan for catch-up growth, and make sure micronutrient gaps (iron, vitamin D, zinc, and B12 are common in IBD) are addressed. The nutritional plan should adapt to where the child is in their disease course - flare, recovery, and remission all need different approaches.

Partial enteral nutrition (using nutritional drinks alongside food) can also play a role in maintaining remission after EEN. The evidence is growing for this approach, and it's something I discuss with families as part of the longer-term plan.

Dietary triggers and the FODMAP question

One of the most common questions I get from families is 'what foods should my child avoid?' The honest answer is: it depends. IBD isn't caused by diet, and blanket food restrictions aren't helpful. But individual trigger foods can worsen symptoms in some children, and working out which foods are genuine triggers (and which aren't) is something a structured dietetic approach can help with.

Low-FODMAP diets are sometimes trialled for children with IBD who have ongoing gut symptoms despite controlled disease. FODMAPs are fermentable carbohydrates that can cause bloating, gas and discomfort in some people. The diet is a diagnostic tool, not a permanent way of eating - it's a structured process that should only be done with specialist dietetic guidance.

I don't recommend starting a FODMAP diet without guidance, especially for children. It's restrictive, it needs to be time-limited, and it needs to be nutritionally adequate. Done properly it can give useful answers. Done badly it just narrows the diet for no reason.

Growth, puberty and long-term outcomes

Growth failure is one of the hallmarks of paediatric IBD, particularly Crohn's disease, as highlighted by Crohn's & Colitis UK. Up to 40% of children with Crohn's have impaired growth at diagnosis. Catching up is a major goal of treatment, and nutrition is central to that. The window for catch-up narrows as puberty progresses, which is why early, active nutritional management matters so much.

Bone health is another long-term concern. Chronic inflammation, poor absorption, steroid use, and low vitamin D all affect bone density. I routinely assess calcium and vitamin D status and supplement where needed. These are things that matter now but also twenty years from now.

The good news, as the BSPGHAN highlights, is that with proper treatment - including proper nutritional management - most children with IBD do well. Growth catches up, puberty progresses normally, and the long-term outlook has improved significantly with modern treatment approaches. My role is making sure the nutrition piece is fully optimised alongside medical management.

Common questions

Persistent diarrhoea (sometimes bloody), abdominal pain, weight loss or poor growth, fatigue, and sometimes mouth ulcers, joint pain or skin rashes. Some children present mainly with growth failure without obvious gut symptoms, which is why IBD should be considered in any child with unexplained poor growth.
A complete liquid feed used as the sole source of nutrition for six to eight weeks to induce remission in active Crohn's disease. It works in around 80% of children with mild to moderate disease. The mechanism isn't fully understood but the evidence base is strong. It's recommended as first-line treatment for paediatric Crohn's in the UK.
There's no single 'IBD diet'. During flares, easily tolerated low-residue foods and sometimes enteral nutrition. In remission, a balanced varied diet with attention to individual triggers. Blanket restriction isn't recommended - it's more likely to compromise nutrition than help.
Diet doesn't cause IBD. Individual foods can worsen symptoms in some people during active disease, and working out which foods are personal triggers is useful. But removing foods without evidence of them being a trigger just narrows the diet for no benefit.
Significantly, particularly Crohn's disease. Up to 40% of children have impaired growth at diagnosis. Active disease, poor absorption, inflammation, and steroid use all contribute. Catch-up growth is a major goal of treatment, and the window narrows as puberty progresses - which is why early nutritional intervention matters.
Crohn's disease is more common than ulcerative colitis in children in the UK. There's also a category called IBD-unclassified (IBD-U) which is more common in younger children. The nutritional implications differ somewhat between types, which is why a specific assessment matters.
Not unless there's a specific reason to. Coeliac disease should be excluded if there's any suspicion, and lactose intolerance can occur secondary to gut inflammation. But preemptive restriction without evidence just compromises nutrition. Investigation should be targeted, not blanket.
IBD is a lifelong condition - it doesn't resolve like a food allergy might. But it can be very well managed, and many people have long periods of remission. The goal of medical treatment in childhood is inducing and maintaining remission, supporting normal growth and development, and minimising the impact on quality of life.
Book a consultation

A clear plan,
built around your little one.

All consultations are online and you can self-refer directly. You'll receive a written plan after every appointment.

How it works
Initial consultation · £90

Thorough assessment & plan

Your first appointment is 60 minutes. It includes a full clinical and dietetic assessment, and you'll receive an agreed, written plan to take away.

Follow-up · £60

Review & adjust

Follow-ups are 30 minutes. We review the plan, problem-solve anything that's come up, and adjust guidance as your child progresses.

What's included
Full dietary and clinical history
Growth chart review and interpretation
Assessment of current intake and feeding patterns
Identification of any nutritional gaps or concerns
A clear, written plan with specific recommendations
Guidance on next steps and when to come back

Currently self-pay only. All fees are VAT-exempt as registered healthcare services. I provide receipts with my HCPC registration details which you can submit to your insurer.