Finding local in-person ostomy support groups can be a wonderful way to connect with others who understand your experiences. Many people with ostomies have never met another ostomate in person, but there are resources available to help you find a nearby group. One recommended resource is the United Ostomy Associations of America website (uoaa.org), which can help you locate support groups in your area. For example, a group in Minneapolis meets monthly, and even after 20 years, attendees continue to learn new things and find value in the meetings. Here are some tips and insights to help you find and connect with a support group:

1. Check multiple sources for meetings:
- Use the United Ostomy Associations of America website (uoaa.org) to find local groups.
- In the UK, look for the Colostomy Association and the Ileostomy Association for listings of local groups.
- In Canada, visit the Ostomy Canada Society website (ostomycanada.ca) for information.
- Local hospital newsletters or community-health bulletins often list ostomy and other support groups.

2. Meeting logistics and alternatives:
- Be aware that some groups may cancel meetings during holidays or schedule them at times that might conflict with work. It's a good idea to verify dates and times in advance.
- If the nearest group is too far away or inactive, consider joining online forums, including those on uoaa.org and other ostomy-related sites, to connect with others.
- If contact information on uoaa.org is outdated, try reaching out to hospitals, WOC nurses, or searching social media for more current details.

3. If no suitable group exists locally, think about starting one yourself. Social media platforms can be a great way to connect with other ostomates in your area and organize regular meet-ups.