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Support for you

This photograph is of two women talking. It is the header image for the 'one to one support' page on the Urostomy Association's website

One to one support

Having a urinary diversion can be daunting, but our trained volunteers can provide reassuring, confidential one to one support, by telephone, face-to-face or through our branches and groups. All our volunteers are urostomates themselves, so can understand your concerns.

This is a photo of two people sitting in a cafe looking at a notebook. It is the header image for the FAQs page on the Urostomy Association's website.

Frequently asked questions

If you're facing, or living with a urinary diversion, you've probably got lots of questions. Do check out our FAQs and see if we can help.

This is a photo of a woman looking at a laptop. It is the header image for the Urostomy Association's page on webinars.

‘Meet the experts’ webinars

Whether you’re considering or already have a urinary diversion, you may have questions about how this might affect your life. We’ve been designing a series of webinars to explore some of the most common topics.

This is a photo of a string of people cut out of paper. It is the header image for the 'local support' page on the Urostomy Association's website.

Local support

In some areas of the UK, local groups offer mutual support and information. These groups have a range of in-person and online meetings.

This photo is of someone holding a mobile phone. It is the header image on the 'Helpline' page of the Urostomy Association's website

Helpline

It's not unusual to feel anxious when you have, or are facing, a urinary diversion. And it isn't always easy to talk to family and friends. But don’t worry, you can call our helpline for support, advice and help.

This photo is of a couple looking at the mobile phone. It is the header image of the Urostomy Association's web page describing its 'Urostomy Association Help and Support' Facebook group

Facebook group

Why not join our Urostomy Association Help and Support Group? It is a supportive community for people living with a urinary diversion or preparing for their surgery. Family members and carers will also find it a helpful.

This is a photo of a laptop. On the screen are the covers of two editions of the Urostomy Association's magazine, The Journal

The Journal

Packed with real life stories, advice, support, top tips and much more, The Journal is written exclusively for people living with, or facing, a urinary diversion. It is published three times a year and available digitally or through your door.

This photo is of a notepad with the word 'events' written on it. It is the header image for page on the Urostomy Association's website which describes the events which urostomates might like to attend

Attend an event

You may like getting together to share tips and experiences. Knowing that others understand what life is like with a urinary diversion can be empowering. On our events page you can see what’s being organised by our groups, branches, suppliers and others.