You might want to think about joining the Canadian bronchiectasis and NTM support group. They are part of the support group network that will be working along with the bronchiectasis care centers in the US. From a recent conference I attended, it looks like they will also be setting up a similar system in Canada. I believe they meet monthly using Zoom. But it’s best to reach out to the group leader Esther so she can put you on the email list. Just another layer of support!!
mailto:Canada@ntminfo.org

Linda Esposito