In the 1970's, Crohn's was little known outside the medical profession. This is the year that our volunteer and supporter, Hilary, received her diagnosis and, in 1985, received an ostomy. Hilary shared her experience with us, from the stigma at the time to the difference in support available then and now.
Hilary's story
Back then, if ever I was asked what was wrong with me I would say it was similar to Colitis, since that was something people at least knew a little about. For fifteen years, I had been on a cocktail of drugs, anal retention enemas, colonoscopies, steroids and various other tests and treatments so as my condition gradually got worse, it became time for something else. When the only remaining option was an exclusion diet, I couldn't face any more and had a full pan-proctocolectomy in 1985. To be honest, I would have had anything done to stop the pain and debilitation, but the stigma attached to stomas was huge. People thought the outcome of this surgery was 'disgusting'.
I kept it quiet at work as 'the bowel' was something we simply didn't talk about. Fortunately, I was an admin supervisor so frequently leaving the office for the loo was something I could do without anybody knowing or being suspicious. In the end, it broke up my 9-year relationship as my boyfriend simply could not cope with my bag, named Boris.
Boris stands for Bag Outside Replacing Internal System
For the first few weeks, I had a stoma care nurse assist me in changing my bag and choosing a model that suited me but then I was on my own. There were no flange extenders, pastes to fill dips and uneven areas around the stoma, convex bags for retracting stomas, seals to aid better adhesion around the stoma, sprays to prevent skin soreness or anything else to ease removal of the bag.
Now, there are all sorts of makes and designs of bag but in those days, bags and associated accessories were limited.
There was also little that I was aware of in terms of support, advice, help or fundraising. However, I was advised to join Crohn's & Colitis when it was in its infancy, known as NACC (National Association for Crohn's and Colitis), and have been a member ever since.
Since then I have not looked back and have had very little trouble with my ileostomy. Nobody knows I have anything wrong with me unless I choose to tell them, and I am happily married to a man who accepts my stoma and medical needs without quibble. Appliance companies are very helpful, as well as stoma nurses up and down the country, although we could do with a lot more of them.
Thanks to Crohn's & Colitis UK, people are much more knowledgeable about the conditions nowadays and we are even able to use disabled toilets without ugly glances from others. So keep up the good work - you've come a long way since 1985, and so has 'Boris'!
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Helpline Service
Temporary closure - 10/06/2026
Our Helpline will be closed from Wednesday 10 June and will reopen at 10am on Monday 15 June.
We may be closed but we have lots of information here on our website.
If you need urgent medical advice you can call NHS 111 or in Northern Ireland phone your local Phone First. In an emergency call 999 or go to your nearest A&E.
If you need emotional support the Samaritans are available 24 hours a day, 7 days a week on 116 123.
We know it can be difficult to live with, or support someone living with Crohn’s or Colitis. But we’re with you. We can give you the right information and support at the right time.
We’re here for everyone.
How Can We Help?
- We can help you understand Crohn’s and Colitis
- Listen and talk about living with IBD
- Help you connect with others in the Crohn’s and Colitis community
- Give you contact details of specialist organisations
- We can support you to live well with Crohn’s or Colitis and provide up-to-date, evidence-based information
Please be aware we’re not medically or legally trained. We cannot provide detailed financial or benefits advice or specialist emotional support.
Please contact us via telephone, email or LiveChat - 10am to 3pm, Monday to Friday (except English bank holidays).
If you need specific medical advice about your condition, your GP or IBD team will be best placed to help.