going on holiday wearing a urostomy bag

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thought i might share my experience of going on holiday after having surgery to remove my bladder due to bladder cancer... i must admit i was a bit hesitant about booking my first holiday after surgery seeing that the rest of my days were bound by having to wear a urostomy bag now.. the obvious hurdle with going to sunnier climates was the act of sunbathing and swimming whilst wearing the bag.. i need not of worried though.. i purchased some bag covers to give the apparatus a slightly better look and to my surprise not many people took notice of it whilst i was working on my tan on the sun loungers although i admit i was a bit self conscious at first.. as for swimming well my fears of the bag coming off in the water were unfounded as well.. in fact it seem to make it adhere better to my skin whilst i was in the pool.. for this i used a waterproof cover with a belt which actually looked quite trendy.. so my message to all new  urostomy patients contemplating a holiday in sunnier destinations this year is go for it ...just booked my third holiday in three years of having the surgery.. happy new year to all

  • Well done.sounds like you have managed your urostomy bag really well and are looking forward to your next holiday. I have been receiving treatment for bladder cancer for five years with chemotherapy, radiotherapy and BCG and therefore, thankfully still retain my bladder. I hope you don’t mind me asking but who do you use for your travel insurance? Garviv

  • When I first went on holiday because I went through tui.the travel agents they asked a series of mandatory questions about medical conditions regarding me and because I wanted to use there travel insurance I had to ring them direct to explain my position..the general view was that with most travel insurances they won't cover for cancer related conditions or injury but will cover for anything else..my condition is a bit different from yours as I am not receiving any treatment now but just being monitored every six months for 5 years to check for any reoccurrence anywhere else on my body..hope this helps

  • Hi  

    It’s great to read of your positive experience on holiday. You may want to post this on the Stoma Support group to give encouragement to others.

    Stoma Support Group

    There are people like myself who have stomas but didn’t have bladder cancer or rectal cancer, and the topic of holidays comes up regularly so more people might read your post there. 

    You might also consider having a look through the insurance group for people with cancer

    Travel insurance Forum

    I don’t use the travel agent insurance but as a community champ I’m not able to recommend a particular company. However, there are lots of recommendations from others on there.

    Here’s to many more holidays!

    Sarah xx


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    Cervical Cancer Forum

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm

  • Since my diagnosis & cystectomy, I have used insurancewith.com & once, their sister company getgoing. You have to fill in a questionnaire to get existing conditions covered. The excess has reduced over the years I have been clear. I prefer to have the cover as I use catheters & would be a big problem if eg lost/stolen in transit. We also declare more minor conditions like high blood pressure. 

    Makes me think it's time to plan a holiday!

  • I take my supplies in my hand luggage so they are always with me. I can get an extra free bag for medical supplies to take as cabin baggage with my usual airline. I have an absolute dread of my case going missing so this gives me peace of mind.

    Sarah xx


    Community Champion Badge

    Cervical Cancer Forum

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm

  • Thanks Teasswill, I will investigate their site tonight. Garviv