Can you ask your surgeon about this? There should be an ET nurse in the hospital where your surgery was performed - he/she should be able to tell you what is available in the community (and there should be a Waterloo chapter of Ostomy Society of Canada - if all else fails, Google them - they will be able to tell you the details of community meetings.) We have meetings in London 5 times a year. I find them REALLY helpful. Also, did you not get any support from LHINS? (used to be CCAC) They should have an ostomy nurse that should be doing home visits for support of new ostomy patients. You may need to call your local LHINS to find out. When I had my surgery, they sent an ET nurse who made 3 home visits, and brought a ton of supplies. Hope this is helpful - good luck.