Dating with a stoma- Sarah's story

1 minute read time.
Dating with a stoma- Sarah's story

As part of the Dating and cancer series, Sarah shares her journey of navigating the dating world since her bowel cancer diagnosis in 2018 and why being open and honest about her stoma bag is important for her.

“I've really welcomed having a stoma bag because my bag saved my life. I was always going to embrace it, but it is something that factors into my dating life. If you're going to be intimate with someone or if you're going to live with someone, you have to have a conversation at some point about the bag.”

Watch the video below to hear Sarah talking about her dating experiences living with a stoma.


If you have a dating with cancer experience you want to share, or have been thinking about starting a new relationship but are feeling worried, join the Let’s talk about dating and cancer discussion thread. It’s a dedicated space for Community members to support each other and share personal experiences with dating.  

You can also join the Bowel (colon and rectal) cancer forum and the Ileostomy, colostomy and stoma support forum to chat to others, ask questions and share personal experiences.

Catch up with Lauren and Mason’s dating and cancer experiences

Lived experiences of dating with cancer: Online Community members and guest storyteller Lauren share their personal experiences. At the age of 25, Lauren was diagnosed with stage 4 Hodgkin lymphoma. As she navigated a cancer diagnosis and treatment, Lauren was also starting a new relationship with Danny. The couple have now been together for six years and recently got engaged.

Dating and cancer- Mason’s story : In 2022, Mason received a diagnosis of an aggressive brain tumour. Mason's dating style has changed as a result of this life-changing event, and he now places a higher priority on developing trust with possible partners and values deeper relationships than ever before. 

Further reading and resources

Anonymous
  • Just to say please add in urostomy as well - bladderless people may still want to date!

  • Hi  

    Thank you so much for your valuable feedback, we really appreciate it.

    Our stoma group is there for anyone with any type of stoma, including urostomy or ileal conduit. If there's any further support you think would be good for us to add, please do let us know.

    This story focuses on Sarah's experience with her stoma following bowel cancer. We can certainly look at featuring future stories which have a focus on experiences of urostomy. Please do let us know if you would like to be part of this, we welcome guest bloggers talking about their experience.

  • I'm long past dating age and have no relevant experience but felt that everything Sarah said also applies to people with other stomas and a simple addition to her story saying so would help others feel included and part of the same constituency. Ie daters with bags.

    Though now I think about it, would those with neobladders etc not also have something to add here too? Daters who are differently configured from the 'average' must be similar regardless of the type of stoma, bag, or other unusual way of producing output.

    tThank you for the suggestion, I might be interested in blogging at some point if I can think of a good angle. But for me dating isn't it.

    Best wishes,

    Latestart

  • Hi Latestart,

    It’s Megan from the Online Community team here. Thank you again for sharing your feedback with us. It’s good to hear you connected with some of Sarah’s story.

    We would love to share more personal stories about the different experiences of people living with all types of stomas. Our Community news blog is a good place to highlight awareness on certain topics and feature different personal stories. The first blog in the ‘Dating and cancer’ series does share a range of different lived experiences from our Community members if you want to read this.

    If you do decide this is something you would be interested in please don’t hesitate to get in touch with the Online Community team by emailing Community@macmillan.org.uk or send a private message to the Moderator account.

    I can see you are an active member of the Bladder cancer forum and I hope you are finding connecting with members of this group to be a comforting source of support. If you need any help using the Online Community or finding additional support, please don’t hesitate to get in touch.

    Best wishes, 

    Megan 
    Macmillan's Online Community team

  • Hi I'd love to tell my story of how fast every thing went for me. in Dec last year I went to the dr for I couldn't poo as normal (I had ulserative colitis for ever ) anyway he referred me to a specialist who put a camera up my back passage and found a large blockage .this was on Mon 16 of Dec 2024 the following day I was sent for a c