Hirschsprungs Family Connections

We provide solace in what can be a frightening disease by peer-to-peer support in an informal environment. Children have the opportunity to forge friendships with Children 'just like' them and the Parent's & Carers have the unique experience of chatting to others with no explanation required!

The primary role of the Colostomy Association is to represent the interests of people with a colostomy. We are experts in living with a colostomy and that experience is available to all colostomates, via personal contact with our volunteers. We are here to provide support, reassurance and practical information to anyone who has or is about to have a colostomy. We strive to raise awareness of what it’s like to have a stoma and what it means to live with a colostomy and by doing this, we hope to

Diversions' is a support network, based in the North West of England, for families with a child or young person living with a bladder or bowel diversion / dysfunction. We provide opportunities for people to experience a range of different fun activities through our regular programme of events. These include outdoor adventures and team building tasks, art work-shops and day trips out.

The Hirschsprung's & Motility Disorders Support Network (HMDSN), is an organization that makes it possible for of ordinary people and families, who's children suffer from Hirschsprung's Disease and other Gastrointestinal motility disorders to support each other. We want to help parents with children who suffer from these Secret Diseases

a charity which provides impartial information about equipment (assistive technology) and services for disabled adults, children, older people and the professionals who support them

 We are an internet based support website for Ostomates of all types. We hope to provide the answers to any problems you may have living with a ostomy whether its leakages, sore skin or just a chat to another Ostomate. We are available online and will take your call anytime you need to talk