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Having a stoma should never stop you from seeing the world. With over 13,500 stoma-forming operations carried out in England each year – whether a colostomy, ileostomy, or urostomy – thousands of ostomates travel confidently, and with the right preparation, you can too.

Whether you are planning a fortnight in the Mediterranean or a long weekend in the Lake District, travelling with a stoma simply requires a little extra planning.

This guide from Secure Healthcare Solutions walks you through everything you need to know, from documentation and packing to airport security and swimming on the beach.

Pre-Travel Planning & Documentation

Good preparation begins weeks before departure, not the night before.

Speak to your stoma care nurse at least four to six weeks ahead of your trip. They can assess whether your stoma is settled enough for travel, offer destination-specific advice, and provide a stoma travel certificate UK – a multilingual document that explains your condition to airport staff and border officials.

Certificates are available free of charge from organisations such as Colostomy UK, the Ileostomy & Internal Pouch Association, and major appliance manufacturers including Convatec, Coloplast, and Hollister.

Ask your GP or consultant for a supporting letter that confirms your diagnosis and lists the medical supplies you carry.

Travel insurance with a stoma requires careful attention. You must declare your stoma and the underlying condition that led to its formation – whether that is Crohn’s disease, ulcerative colitis, bowel cancer, or another diagnosis.

Failing to disclose a pre-existing condition can invalidate your entire policy. Specialist insurers recommended by stoma charities often offer more competitive premiums than high-street providers.

Ensure your policy covers emergency medical treatment, repatriation, and trip cancellation due to a flare-up.

If you are travelling to an EU country, apply for a UK Global Health Insurance Card (GHIC) through the official NHS website. The GHIC provides access to state-provided healthcare but is not a replacement for comprehensive travel insurance.

Finally, research your destination. Note the nearest hospital, check whether your appliance manufacturer has a local distributor, and write down your product codes – these are essential if you need emergency replacements abroad.

The Essential Stoma Travel Packing Checklist

The golden rule: pack at least double the supplies you would normally use. Heat, dietary changes, and travel stress can all increase the frequency of bag changes.

Stoma supplies:

  • Pouches (pre-cut before departure – scissors are not permitted in hand luggage)
  • Baseplates and barrier rings or stoma paste
  • Adhesive remover wipes (avoid aerosol sprays, which may be restricted)
  • Skin barrier wipes and deodorising drops
  • Disposal bags, hand sanitiser, and a small mirror
  • Flange extenders and waterproof tape (essential for swimming)
  • Oral rehydration sachets such as Dioralyte – particularly important for ileostomates

Documents:

  • Stoma travel certificate and GP letter
  • Travel insurance policy
  • GHIC card (for European travel)
  • Product codes and supplier contact details
  • Repeat prescription copy

Always carry your essential supplies in your hand luggage. If your checked bags are lost or delayed, you must be able to manage independently. Split any surplus between your suitcase and a travel companion’s bag.

Flying and Airport Security Tips

Flying with a stoma bag is straightforward once you know what to expect. Contact your airline at least 48 hours before departure – many carriers permit an additional piece of hand luggage specifically for medical supplies, in line with Civil Aviation Authority (CAA) guidance. Request written confirmation and keep it with your boarding pass.

Going through airport security with a stoma is far less daunting than most people imagine. You will not be asked to remove or expose your pouch.

If the body scanner detects your appliance, you may be invited for a secondary check – you have the right to request a private search conducted by a staff member of the same sex.

Present your stoma travel certificate proactively; it prevents awkward explanations and speeds the process along.

Empty your pouch just before entering the security queue and wear loose, comfortable clothing. Consider collecting a Hidden Disabilities Sunflower lanyard from the airport’s assistance desk – it is a nationally recognised signal that you have a non-visible disability and may need additional time or support, without having to explain your condition aloud.

It is also worth carrying a RADAR key for accessing locked accessible toilets across the UK, and a Can’t Wait card from the Bladder & Bowel Community, which signals toilet urgency to staff and businesses.

During the flight, book an aisle seat near the lavatory. Stay well-hydrated – cabin air is extremely dry – and avoid carbonated drinks and gas-producing foods before boarding.

Swimming, Beach, and Hot-Weather Advice

Swimming with a stoma is completely safe. Your pouch is waterproof and designed to withstand immersion in pools, the sea, and freshwater.

Apply your bag at least one hour before entering the water to allow the adhesive to bond fully, and empty it immediately beforehand. Cover the charcoal filter with the waterproof sticker supplied in your box to prevent it becoming waterlogged.

For extra security, use flange extenders or waterproof tape around the edges of your baseplate. Many of these accessories are available on NHS prescription – speak to your stoma care nurse before you travel.

Swimwear with high waists, ruched patterns, or darker fabrics offers natural discretion, and specialist stoma-friendly brands provide additional support.

Hot and humid weather can weaken baseplate adhesion, so expect to change your pouch more frequently. Keep supplies in a cool bag at the beach, drink plenty of water throughout the day, and carry rehydration sachets.

Avoid excessive alcohol and caffeine, which accelerate fluid loss – a particular risk for anyone with an ileostomy.

Staying Well Abroad – Food, Drink, and Emergencies

Drink bottled water in countries where tap water quality is uncertain, and avoid ice in drinks. Introduce local cuisine gradually; sudden dietary changes can significantly alter your stoma bag output. Be cautious with raw salads, shellfish, and street food in regions with lower hygiene standards.

Traveller’s diarrhoea is a common risk. If you experience a stomach upset, increase your fluid intake, consider loperamide (if previously agreed with your GP – it is not suitable for all stoma types), and switch to bland, low-fibre foods.

With an ileostomy, dehydration can escalate rapidly – seek medical attention if vomiting or diarrhoea persists beyond 24 hours. Carry oral rehydration sachets at all times.

Should you run low on supplies, contact your appliance manufacturer’s international helpline. Most major brands – including Convatec, Coloplast, and Hollister – maintain global distributor networks and can arrange emergency delivery. In an EU country, present your GHIC at a local hospital or pharmacy, where some stoma supplies may be dispensed in an emergency.

For further support, the Bladder & Bowel Community and Colostomy UK both offer helplines with advice from people with lived experience.

Enjoy Your Holiday with Confidence

Travelling with a stoma is not only possible – it is something to look forward to. With your checklist packed, your documents in order, and a little forward planning, there is no reason your stoma should hold you back from the holiday you deserve. Start with a short trip if you are feeling cautious, and build from there.

If you need specialist support before or after your travels, Secure Healthcare Solutions offers expert stoma care in the UK through experienced stoma care nurses who understand your needs. Visit our website to find out how we can help you live life to the fullest.

References

  • https://www.colostomyuk.org/information/travel-advice/
  • https://www.nhs.uk/conditions/colostomy/
  • https://www.bladderandbowel.org/help-information/just-cant-wait-card/
  • https://hdsunflower.com/
  • https://www.iasupport.org