As medications and healthcare for those with Cystic Fibrosis have improved, it is now common for people with Cystic Fibrosis and their families to travel abroad. However there are some issues to consider when travelling if you or a family member has Cystic Fibrosis.

• Travel insurance
  
• Medication - including taking sufficient, sterilising tablets, salt tablets, antibiotics etc
• Air travel
• Oxygen
• Nebulisers and voltage
• Clothing
• Visits to theme parks
• Driving abroad
• CF Centres abroad
• Financial assistance
• Specialised holiday funds (such as CF Holiday Fund)

For further information, please see Contact a Family who have a holiday factsheet and can provide a list of 'wish' granting organisations.