My youngest son was diagnosed with Crohn's Disease when he was only 7 years old. Within the first year of his being diagnosed I attended a seminar in Wellington, organised by CCNZ, where I had the opportunity to meet and get to know the speakers and other support people. From there I was recruited as the coordinator of the Tauranga Support Group. My son was so young when diagnosed that we really just wanted to meet other people with children who had Crohn's. CCNZ’s Camp Purple has been the best thing ever for him. In recent years my husband was also diagnosed with Crohn's and now we are awaiting confirmation for my oldest son as well. Very busy household and only 1 toilet!!!

It has taken a few years to get momentum going with the support group. We try to meet every 2 - 3 months, whether it's a bowling night, coffee catch up or a drink at the local pub. I'd like to create a safe place for all IBD patients and their families where they feel they can talk and be part of a group of people who understand, offer experience and listen.

In recent catch ups I have had a few fantastic people offer to help out. We are in the process of organising a speaker for our next catch up in the new year.

If you are interested in helping organising any catchup's, please get in contact at bop@crohnsandcolitis.org.nz