Travel & IBD

If you have Crohn’s Disease or Ulcerative Colitis (the two main forms of Inflammatory Bowel Disease - IBD) you may find the thought of travelling daunting. A change of climate, water, or food can upset anyone’s bowels. Yet many people with Crohn's or Colitis travel widely, both in the UK and abroad. They may go for a short break or a long holiday lasting several weeks or months. With careful planning ahead it should be possible for you to travel to most places. Before you leave, speak to your doctor about a flare-up plan. This will mean you know what to do if your symptoms worsen while you are away.

This information sets out to answer some of the questions that you may have when thinking about going on holiday or on a business trip. It also includes suggestions for people who have a stoma or have had surgery. 

It is important to arrange travel insurance in case you need medical treatment when abroad. This is particularly the case if you are travelling to countries that don’t have healthcare agreements with the UK. For example, costs are high in the USA. For further information, and for a country-by-country guide, see nhs.uk/nhsengland/healthcareabroad

For travel to most parts of Europe, you can get a free European Health Insurance Card (EHIC). The card entitles you to reduced-cost or free treatment in most European countries. However, you may still want travel insurance for other potential costs, such as emergency travel back to the UK. When the UK leaves the European Union, it could mean that UK residents will no longer have access to the EHIC scheme. You can check before you travel, and apply for the card online at ehic.org.uk or by telephone on 0300 330 1350.

If you do not mention your Crohn's or Coltis when you are arranging an insurance policy, you may find that your cover is invalid or that you have problems should you need to make a claim.

Some insurance companies will expect you to confirm with your doctor that you are fit to travel. It may be more difficult or expensive to get cover if you have had surgery or been admitted into hospital in the last few years. This may also be the case if you are waiting for the results of tests or investigations. In some cases, the insurance company may agree to cover you but exclude any problems related to your Crohn's or Colitis. However, if your Crohn's or Colitis is under control you may find it relatively easy to take out an insurance policy. You may find it helpful to look at our information sheet Insurance and IBD, which gives more details about travel insurance and includes a list of companies suggested by Crohn’s & Colitis UK members.

If you become ill during your travels and wish to claim on your insurance, you should keep receipts for everything, including things like taxi fares to hospital.

38% of people do not get travel insurance to cover their IBD & 76% have had to pay a premium to cover their IBD.

Travel with IBD survey, 2017

Vaccinations may be needed or recommended for travel to certain countries. Check with your doctor or travel clinic to find out which vaccines you should have. Be sure to mention your Crohn's or Colitis, and provide a list of your medications, including dosages. Some vaccine schedules take time to complete, so you should find out what you may need at least 6-8 weeks in advance.

To find out what vaccinations you may need, you can visit the NHS Fit for Travel website.

It is a good idea to take your vaccination record card with you when you travel. If you are travelling to a country where a yellow fever certificate is required, you must take this with you, or you may be refused entry.

If you are on certain drugs for your Crohn's or Colitis, you may find that you cannot have live vaccines. This is because some of the drugs prescribed for Crohn's or Colitis can weaken the immune system. These include:

• steroids, such as prednisolone, budesonide and hydrocortisone
• immunosuppressants, such as azathioprine, 6-mercaptopurine and methotrexate
• biologics, such as infliximab (Remicade), adalimumab (Humira), vedolizumab (Entyvio), ustekinumab (Stelara) and golimumab (Simponi)

If you are taking any of these medications, you should seek specialist advice.

In the UK, live vaccines include:
• yellow fever
• BCG (tuberculosis)
• oral typhoid
• measles, mumps and rubella (either as individual vaccines, or as the triple (MMR vaccine)
• chickenpox (varicella)
• rotavirus (infants only)
• flu nasal spray (children only). The annual flu jab is not a live vaccine and is recommended for people with IBD.

If you are unable to have a yellow fever vaccine and are travelling to a country with a yellow fever vaccination certificate requirement, you can ask your doctor for a medical exemption letter. However, even with such a letter, some countries may refuse entry. If you are travelling to a country where there is a yellow fever risk and you cannot have the vaccination, you may be at risk of acquiring yellow fever. Seek advice from a yellow fever vaccination centre. It may be in your best interests to choose a different destination. If you have stopped taking a drug that alters your immune system, you may beable to have a live vaccination after waiting 3-6 months, depending on the drug.

Before starting a drug that alters your immune system, talk with your IBD team about potential travel plans to ensure your travel vaccinations are up to date before your treatment starts.

If you have recently had a live vaccination, it is recommended that you wait at least three weeks before starting a treatment that alters your immune system.

Inactivated vaccines, such as hepatitis A and rabies, contain a killed version of the virus or bacteria. Inactivated vaccines are considered safe, but they may not be as effective when taking drugs that alter your immune system.

45% of people with IBD did not seek advice when travelling abroad.

Travel with IBD survey, 2017

If you are travelling to an area with malarial mosquitoes, you may be advised to take an anti-malaria medication. Most tablets have to be started before you travel and continued for up to four weeks after you return. There are a number of different types of anti-malarials, and there may be side effects that could affect your Crohn's or Colitis. There can also be adverse interactions between some anti-malarials and some drugs used for Crohn's and Colitis. Your doctor or travel clinic can help you decide which anti-malarial tablets are suitable for you.

Mosquito bite avoidance
Preventing mosquito bites is just as important as taking anti-malarial medication. There are many other infections that can be transmitted through mosquito bites, such as dengue fever and zika, which do not have a vaccine or preventative medication.

Different types of mosquitoes transmit different infections – and these bite at different times of day, so protection is recommended at all times. You can help to protect yourself by wearing light-coloured, loose clothing to cover your arms and legs, and using an effective insect repellent, such as one containing DEET (N,N- diethyl-m-toluamide) of at least 20% concentration. Read and follow instructions carefully when applying DEET.

Sunscreen may not be as effective if applied after insect repellent. When you need to use both, apply the sunscreen first.

More information can be found on the NHS Fit for Travel website.

It may help to have certain medical documents and information with you when you are away. Examples include:

• A letter from your GP or consultant confirming that you are fit to travel. You may have to pay a fee for this.
• A medical summary of your condition, history and any known allergies, as well as a plan for what to do if you have a flare-up. Talk to your doctor about these before you leave. You may want to have the information translated into the language of your destination, particularly if English is not commonly understood. You could try using a phrase book or Google Translate to help you.
• A list of your medications, including the generic names of drugs (for example, mesalazine for Asacol or Pentasa) and a photocopy of your prescription.
• A list of key words and phrases about your condition and medication in the local language.
• One of our Crohn’s & Colitis UK Can’t Wait Cards in the language of your destination. You can call our Information Line on 0300 222 5700 to request one.
• The details of your doctor and IBD team, including phone numbers and email addresses.
• If possible, the name and contact details of the doctor and clinic you would hope to visit, should you need to. Your doctor or IBD team may be able to help with this, or you may be able to find details of healthcare professionals in your travel destination on the IBD Passport website.
• If you use steroids, a steroid card or ‘MedicAlert’ bracelet. If there is an emergency, this alerts the person treating you to your condition and medication. You can obtain a card from any pharmacy or a bracelet from the MedicAlert Foundation on 01908 951045 or at medicalert.org.uk.  You can also wear a MedicAlert bracelet for other medications.
• A dietary card in various languages, if you are on a restricted diet. See the DietaryCard in Other organisations, below, for more details.

When I go away, I take an up-to-date clinic letter, my insurance details, European health card and copies of prescriptions for my drugs. 

Chris, age 26
Diagnosed with Crohn's in 2013

Packing medicines
Try to take enough medication for your whole trip, as well as extra in case of delays, to ensure you do not run out. If your medication requires refrigeration, such as with adalimumab (Humira) and golimumab (Simponi), you could store it in a small cool bag, obtainable from chemists, or in a Frio cooling wallet that works without refrigeration. See Other organisations for information about Frio. Note that Humira can be kept at room temperature (25°C) for up to 14 days – but it must be used within the 14 days or thrown away.

Plan ahead if you need to get new supplies of medication while you are away. Take a list of your medications, and consider checking with the relevant pharmaceutical companies about whether your medications are available in the countries you plan to visit. Your IBD team and pharmacists may be able to advise you. If your medication cannot be obtained where you are going, you could ask your doctor for a private prescription and buy extra supplies in the UK from a pharmacy.

You may also want to take a good supply of any over-the-counter medicines you are using. This could include anti-diarrhoeals such as Imodium or Lomotil, anti- spasmodics, such as Buscopan or Colofac, rehydration sachets and painkillers. Anti-diarrhoeals should not be taken if you are having a Crohn's or Colitis flare-up.

Taking medicines abroad
If you are travelling abroad, the government advises you to keep your drugs in their original packaging, along with the Patient Information Leaflet, to show at customs. You may also need to show your letter from your GP or consultant, and a copy of your prescription.

You should carry your medication in your hand luggage when flying, in case your baggage is lost. It may also be a good idea to pack a supply of medication and a copy of your prescription in your hold luggage, in case you lose your hand luggage. Hand luggage restrictions mean that if you have more than 100ml of medicine, including liquids, gels, creams or pastes, you will need to show a letter from your doctor or a copy of your prescription.

Before you fly, check with your airline to find out whether there are any other restrictions or rules that will affect travelling with your medications. This may apply if you need to take syringes and needles in either your hand luggage or checked-in bags. You may wish to buy a travel-sized sharps bin. You could then take it to a medical centre with sharps disposal in the country you are visiting, and show them the letter from your doctor or consultant. If it’s a short trip, you could bring the syringes back with you in the sharps container and dispose of them in the usual way.

Some countries have restrictions on bringing in drugs for personal use. Check  with the embassy of the country you will be visiting to find out whether this applies to your medications. Details of foreign embassies in the UK can be found on the Foreign Office website.

You may need a personal licence to take your medicines abroad, as some prescription medicines contain drugs subject to control under the UK’s Misuse of Drugs Act. Many medicines prescribed for IBD do not contain controlled drugs. However, some people with Crohn's or Colitis may be taking medications such as codeine or morphine that do contain controlled drugs. If you are unsure about whether you need to obtain a licence, contact the Home Office Drugs Branch on 020 7035 6330 or see their website. Personal licences are only required if you are leaving the country carrying supplies for three months or more. You should apply at least 10 days in advance to ensure that your licence is processed before you leave.

If you are travelling across different time zones, you may wonder about when to take your medication. You may choose to continue taking your medicines at the same time as you have been in the UK. Another option could be to gradually adjust the timing of your medication to the country you will be in, and do the same on the return journey. It might be helpful to set an alarm so you don’t forget to take your medication. Your IBD team or pharmacist can help you plan for this.

I always make sure I am stocked up with medication before I go away. And I pack my medication with a copy of my prescription in my hand luggage, just in case my cabin luggage were to get lost.

Andy, age37 
Diagnosed with Colitis in 2007


 

If you are on enteral nutrition (liquid diet), a powdered product may be easier to carry and will take up less space in your luggage. However, you will have to get  a change of prescription from the liquid to powdered form. When making up the product at your destination, make sure the water is of a sufficiently high quality, or use bottled water.

For advice on transporting either liquid or powdered diets, see the sections Packing medicines and Taking medicines abroad.

Regardless of the mode of transport you use on your trip, there are issues that you may wish to consider.

You can get a RADAR key to open accessible toilets across the UK from Disability Rights UK. A Euro key for toilets for disabled people in Germany, which also works for toilets in some other European countries, can be bought from CBF Darmstadt. For details, see Other organisations.

When travelling by bus, train or plane, you may want to check whether there is a toilet on board, and, if possible, book an aisle seat close to it. It may also be helpful to print a copy of your travel details and connections, and bring your own snacks and water.

Travelling by car
If you are travelling by car, you may wish to check the location of toilet facilities when planning your route. Toilets can often be found in tourist information centres, supermarkets and fast food restaurants, as well as service stations. The IBD Passport website has details of toilet map apps for different countries. Some people carry a travel potty in their vehicle for peace of mind when travelling on long journeys.

If you have a Blue Badge, you can also use it in the European Union (EU). See www.gov.uk for guidance on using a Blue Badge in the EU and the rules for each country.

Travelling by train
If needed, you can usually get extra support when travelling on the train, for example, help with carrying luggage and finding the right platform. Although you can ask for help at the station, it is a good idea to request assistance in advance. If you are travelling in the UK, you can call National Rail on 0800 022 3720. If you are travelling by Eurostar, you can call 03432 186 186 to arrange additional travel support.

If you receive disability benefits, such as Personal Independence Payments (PIP), you may also be eligible for a Disabled Persons Railcard that gives you discounted rail travel in the UK.

You can find country-specific guides for train travel abroad at www.seat61.com.

Travelling by plane
Airlines and airports have varied provisions for providing care. You should get in touch with your airline at least 48 hours before you fly to let them know your requirements or any additional assistance needed. Your airline may ask you and your doctor to fill out a Medical Information Form (MEDIF) – for example, if you’ve recently had surgery or suffer from anxiety or depression. A MEDIF is only valid for the flight you are taking and must be completed before you fly.

Some airlines request this information up to 72 hours before a flight. If your condition is relatively stable and you fly regularly, you may be able to get a Frequent Traveller Medical Card (FREMEC) that can be used for multiple journeys.

Many UK airports now offer a lanyard scheme for people with hidden disabilities to discreetly alert staff to their needs. The lanyards are available even if you do not need to use the special assistance service and may give you access to priority lanes at security.

You can usually pre-arrange your in-flight meals for any particular dietary requirements, such as dairy-free or low-fat. Cabin air can be very dry, so drinking plenty of water and avoiding alcohol and caffeine should help to prevent dehydration. If you are going on a long flight, you might want to consider taking an anti-diarrhoeal beforehand. This is not recommended if you are having a Crohn's or Colitis flare-up.

70% of people with IBD worry about toilet facilities while travelling.

Travel with IBD survey, 2017

If you have an ileostomy or colostomy, you may have particular concerns about travelling. With careful planning, having a stoma should not prevent you from taking a trip.

It is important to take ample stoma supplies. You are likely to be eating differently, and may have to change your appliance more often than usual, especially in hotter climates. You may need to take more supplies than you think you will use – some people suggest twice as much as normal. You could check whether your supplier delivers abroad. If you are travelling by air, taking your supplies in your hand luggage ensures that you are not without them if your luggage is lost. You may not be able to take scissors in your hand luggage, so make sure to pre-cut your adhesive base plates to size.

Colostomy UK, the IA (The Ileostomy and Internal Pouch Support Group), and some stoma companies provide travel certificates explaining your essential needs in different languages. This can be especially useful when checking in at the airport or going through security. It may be helpful to change or empty your pouch just before you enter security. You shouldn’t be concerned if you are asked to have a whole body scan. The image produced by the scanner will consist of a mannequin-style, or ‘gingerbread man’, diagram and will not contain any recognisable personal features. While the scanner may detect your stoma, airport staff should be trained to recognise this and act sensitively.

Before a long journey, try to avoid food or drink that could cause excessive wind or upset. Pressurised air in the cabin can expand gasses in the body, and there is a slight risk that it may cause more gas in your bag. Some stoma appliances have a filter to enable air to escape and prevent embarrassing odours. If your stoma does not have this, it may be worth contacting your stoma company to see if a filter is available.

Some people prefer to use drainable bags while they are away, as these may be easier to empty, especially if local foods are likely to trigger traveller’s diarrhoea. Ensure you take the usual travel precautions regarding food and water hygiene (see Preventing traveller’s diarrhoea).

For detailed information about travelling with a stoma, you can visit the IA or Colostomy UK websites or speak to your stoma nurse.

I was going through security in a Polish airport when the guard asked to body search me and my hand luggage. I was a bit apprehensive as it was my first time travelling since my ileostomy surgery. Fortunately, I had a travel leaflet for patients with a stoma, which was translated into many languages. I showed the guard and he took me to a private room and did the necessary checks there.

Carl, age 35
Diagnosed with Crohn's in 2015


 

After any surgery, doctors usually recommend putting off travel until you are able to walk around easily and to sit comfortably for the duration of a journey. Recovery will be different for everyone. This may be after 3-4 weeks, but it could be more or less depending on the type of surgery and your general condition.

If you have had abdominal surgery and intend to drive, you will be advised to wait until you are able to make an emergency stop with confidence. This can take several months. You may not be covered by your car insurance if you drive before you are fully recovered.

Following recent surgery, pressurised cabin air could cause pain and stretch your wound. In line with advice from the UK Civil Aviation Authority, many airlines restrict air travel for up to 10 days after surgery, depending on the type of operation.

You are also at increased risk of deep vein thrombosis after surgery. See the next section for further information.

DVT or blood clots can be a risk for anyone sitting still on a long journey. Flights lasting over four hours are thought to be more likely to cause blood clots, but long journeys by car, bus or train can also put you at danger. People with Crohn's or Colitis have an increased risk of blood clots. You may also be at risk if you have recently had surgery. You can reduce this risk during the journey by:

• wearing loose fitting, comfortable clothing
• drinking plenty of fluids but avoiding alcoholic and caffeinated drinks before and during the journey
• avoiding smoking
• rotating your ankles and flexing your calf muscles regularly
• taking regular deep breaths
• walking at regular intervals around the plane cabin or train, or during stops on bus and car travel
• wearing travel compression socks/stockings – it is vital that they are properly fitted by a doctor or pharmacist

You may want to talk to your IBD team about your risk of developing DVT – and whether you should wear compression stockings or take anti-coagulant medication.

You may find it helpful to pack an ‘emergency travel kit’ containing everything needed to clean up in case you have an accident. This could contain:

• a supply of pads, pants, alcohol-free wet wipes, tissues, sanitary disposal bags
for soiled pants, disposable gloves and an antibacterial handwash
• a small mirror (useful to check that you are clean)
• a couple of clothes pegs to keep your clothes out of the way if you need both hands to get clean 
• an aerosol neutraliser to disguise odour
• if you are prone to sore skin, a cream such as zinc and castor oil
• a toilet roll and a change of clothes

If you are travelling by air, the kit can be packed in your hand luggage. If you have neutraliser spray in an aerosol canister, check with the airline whether you can take it on board.

My emergency kit is partly for my peace of mind. It makes me feel less nervous knowing that I have everything I need with me.

Gillian, age 39
Diagnosed with Crohn's in 2002

You may wish to ensure that any accommodation you are booking has an en-suite toilet. Your travel agent should know, or it may be worth contacting the place you are staying and asking for written confirmation. Information about accommodation for people with medical needs or disabilities is available from various organisations, such as Tourism for All, Contact and Disability Rights UK.

If your medication needs to be kept in the fridge, call ahead to check that you’ll have access to one where you’re staying.

Some people worry about having an ‘accident’ when away from home. You could take a towel or disposable bed pad to put under you while you sleep. You might also find it helpful to check on laundry arrangements beforehand. If you need to do your own washing, it can be useful to take travel wash, a folding coat hanger, a portable washing line and a few pegs.

Risk of developing traveller’s diarrhoea
Traveller’s diarrhoea is defined as three or more loose stools in a 24-hour period, often accompanied by other symptoms, including stomach cramps, fever and vomiting. It is usually caused by bacteria, parasites or viruses in contaminated food and water. Anyone travelling abroad is at risk of getting this, especially in less developed countries. Having Crohn's or Colitis shouldn’t make you more likely to get traveller’s diarrhoea. If you are taking drugs that weaken your immune system you may experience more severe traveller’s diarrhoea (see the Vaccinations section for a list of drugs). Everyone should be careful about what they eat and drink while travelling.

Preventing traveller’s diarrhoea
The following tips may help you reduce the risk of developing traveller’s diarrhoea:

• Wash your hands with soap, and dry by air or on a clean towel before eating. You could carry a supply of anti-bacterial wipes or hand gel for places without washing facilities.
• Drink bottled water (ensuring the seal is not broken) or water that has been boiled. It is worth bearing in mind that you will need to boil the water for longer if you are at high altitude. Sterilising tablets, if used correctly, are an alternative way of purifying water. You may wish to carry a supply of them, as they kill most bacteria.
• Exercise caution with fresh fruit juices and ice cream because the water used to make them may not be safe.
• Use bottled or sterilised water to clean your teeth and when preparing food.
• Avoid ice in drinks unless you are sure it is made with safe water.
• Peel all fruits and eggshells yourself. This includes tomatoes.
• Avoid unpasteurised dairy products.
• Avoid raw vegetables and salads, and foods that may be undercooked, such as steaks and burgers, and foods that have been kept warm.
• If using street vendors and kiosks, ensure food is cooked fresh and served immediately while still hot.
• Avoid shellfish as these can easily be contaminated.
• Avoid swallowing water while swimming.

For more information on food hygiene and purifying water, visit the NHS Fit for Travel website.

Treating traveller’s diarrhoea
The symptoms of traveller’s diarrhoea can be similar to those of Crohn's or Colitis. However, traveller’s diarrhoea often passes within four days. Drinking plenty of liquids replaces the fluids lost by diarrhoea, and prevents dehydration, but be careful of ice-cold, alcoholic, caffeinated or citrus drinks, which can aggravate diarrhoea. Rehydration drinks, which can be bought from pharmacies in small sachets, may also be used.

As you improve, you should try to eat small, light meals. It may help to eat bland food, such as bananas, plain toast, boiled rice, soup, chicken and potatoes.

Rest should help you feel better. If you have to keep travelling, you could take an anti-diarrhoeal to help stop the symptoms. However, this is not recommended if you have a flare-up of your Crohn's or Colitis, or if you’re suffering from a fever or bloody diarrhoea.

Bloody diarrhoea could either be caused by an Crohn's or Colitis flare-up, or a bacterial infection that needs treatment with antibiotics. For such an infection, UK doctors generally recommend taking a course of antibiotics, such as ciprofloxacin, or, if you’re travelling to South Asia or South East Asia, azithromycin .

Talk to your doctor if you feel that you might be at risk of developing traveller’s diarrhoea – and whether it may be helpful to take a course of antibiotics with you to use if necessary.

For more suggestions on how to cope with diarrhoea, see our information on Diarrhoea and Constipation.

66% of people with IBD had an alteration in bowel symptoms whilst abroad.

Travel with IBD survey, 2017

In hot weather, if you have had diarrhoea, or if you’re more active than you usually are, you will need to take care not to become dehydrated. Symptoms of dehydration include thirst, a dry mouth, headaches, dark-coloured urine and tiredness. It helps to avoid strenuous exercise during the hottest hours and to drink plenty of non-alcoholic liquids. At least 8-10 average glasses a day are recommended in the UK, with more in hotter climates and when sweating. You can find more information on how to avoid and treat dehydration in our Dehydration information.

While it is important for everyone to protect themselves from the effects of the sun, you will need to take even more care if you are on immunosuppressive drug treatments for your Crohn's or Colitis.

These include:
• adalimumab (Humira)
• azathioprine and mercaptopurine
• ciprofloxacin
• golimumab (Simponi)
• infliximab (Remicade)
• methotrexate

These treatments make your skin more sensitive to sun damage, and may increase the risk of skin cancer. You should use a high skin protection factor sunscreen (SPF 30 or above, with a 4- or 5-star rating that protects against UVA and UVB), avoid being in the sun between 11am and 3pm, stay in the shade and cover up as much as possible with clothing and a wide-brimmed hat.

Travelling can be demanding on anyone whether or not you have Crohn's or Colitis. Some people will find a change in routine or diet, dealing with jet lag or just being in unfamiliar places stressful. For others, stress may come from the excitement of being in a new place and wanting to see and do everything. There may be the temptation to do too much or to eat and drink things you wouldn’t normally have. While you should make the most of your trip, it’s important to know your limits. Don’t be afraid to slow down and take time out when you need it. You may find it helpful to continue doing whatever you do to relax, maintain your exercise routine and generally follow your diet plan. Try to get enough sleep each night – and take a nap during the day if you need it.

Simply taking the time to plan ahead may help you to feel prepared and reduce stress. Research your destination and get familiar with how you’ll be travelling and where you’ll be staying. Speak to your doctor about your travel plans and discuss your most pressing concerns and symptoms. Your doctor can help you decide what medication to take with you, plan what to do in case of a flare-up, and advise on how to best make the most of your time away.

You might find it helpful to read our publications Fatigue and IBD, Food and IBD and Living with IBD.

The most important thing for me has been learning how to make sure I was prepared with everything I might need, without being daunted by all the ‘what ifs’. 

Kate, age 27
Diagnosed with Crohn's in 2005


 

We offer more than 50 publications on many aspects of Crohn’s Disease, Ulcerative Colitis and other forms of Inflammatory Bowel Disease. You may be interested in our comprehensive booklets on each disease, as well as the following publications:

Living With Crohn's or Colitis
Fatigue
Taking Medicines
Managing Bowel Incontinence
Living With a Stoma

Health professionals can order some publications in bulk by using our online ordering system. If you would like a printed copy of a booklet or information sheet, please contact our helpline.

Our helpline is a confidential service providing information and support to anyone affected by Crohn's or Colitis. Our team can:
• help you understand more about Crohn's or Colitis, diagnosis and treatment options
• provide information to help you to live well with your condition
• help you understand and access disability benefits
• be there to listen if you need someone to talk to
• put you in touch with a trained support volunteer who has a personal experience of Crohn's or Colitis

Call us on 0300 222 5700 
Email helpline@crohnsandcolitis.org.uk
Use our LiveChat 

Crohn’s & Colitis UK Forum
This closed-group community on Facebook is for everyone affected by Crohn's or Colitis. You can share your experiences and receive support from others.

Crohn’s & Colitis UK Patient Panels
IBD Patient Panels, which are supported by Crohn’s & Colitis UK, are groups of people with Crohn's or Colitis who use their perspective as a patient to work with their IBD healthcare team to help improve their hospital services. For more information on patient panels, please read our information leaflet or contact our Patient Engagement Team.

Crohn’s & Colitis UK Local Networks
Our Local Networks of volunteers across the UK organise events and provide opportunities to get to know other people in an informal setting, as well as to get involved with educational, awareness-raising and fundraising activities. You may find just being with other people and realising that you are not alone can be reassuring. Families and relatives may also find it useful to meet other people with Crohn's or Colitis. All events are open to members of Crohn’s & Colitis UK

ABTA – The Association of British Travel Agents
ABTA Ltd, 30 Park Street, London SE1 9EQ
0203 117 0599
Useful travel information and specific advice for disabled travellers.

CBF Darmstadt
Euro Key for purchase.

Colostomy UK
Enterprise House, 95 London Street, Reading, Berkshire, RG1 4QA
0800 328 4257

Contact
209-211 City Road, London EC1V 1JN
Helpline: 0808 808 3555
Information about holidays and accommodation for families with disabled children.

European Health Insurance Card: Automated Application Service
0300 330 1350

Department for Transport
Department for Transport, Great Minster House, 33 Horseferry Road, London SW1P
4DR
0300 330 3000

DPTAC – Disabled Persons Transport Advisory Committee
Email: DPTAC.Enquiries@dft.gsi.gov.uk

DietaryCard
3 Inchcross Drive, Bathgate, West Lothian EH48 2HD
01506 635358

Disability Rights UK
Ground Floor, CAN Mezzanine, 49-51 East Road, London, N1 6AH

RADAR keys for purchase.
EFCCA – European Federation of Crohn’s & Ulcerative Colitis Associations

Foreign & Commonwealth Office
0207 008 1500

Frio UK Ltd
Whiteleys, Little Treffegarne, Haverfordwest, SA62 5DY
01437 741700
Supplies medication-cooling wallets and travel-sized sharps bins.

Home Office Drugs Branch
020 7035 6330
Information on controlled drugs, licenses for taking medicines abroad and embassy contact details.

IA (The Ileostomy and Internal Pouch Support Group)
Danehurst Court, 35 - 37 West Street, Rochford, Essex, SS4 1BE
0800 018 4724 (freephone) or
01702 549859

IBD Passport
Email: info@ibdpassport.com
One stop travel advice and information for people with IBD.

The Man in Seat Sixty-One
Country-specific guides for travelling by train abroad.

MedicAlert Foundation
327 Upper Fourth Street, Milton Keynes, MK9 1EH
01908 951045

National Travel Health Network and Centre
Information on health and travel abroad.

NHS fitfortravel
Provides health advice for travellers on a range of topics.

NHS Healthcare Abroad
Provides information on medical care abroad.

PIE Enterprises
20 Ropemaker Street, London, EC2Y 9AR
0207 952 0450
Website for people with restricted mobility that sells maps with information such as parking for Blue Badges.

Public Health England
A government agency to protect and improve the nation’s health and wellbeing, and address health inequalities. It produces guidelines for travellers from the UK, such as prevention of malaria.

Tourism for All
7A Pixel Mill, 44 Appleby Road, Kendal, Cumbria, LA9 6ES
0845 124 9971

World Health Organisation
Directing and coordinating authority for health within the United Nations system.

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Last reviewed: December 2017