i've joined a few FB diabetes support groups and i'm finding it helpful in so many ways to hear of others experiences and to answer and ask questions, share feelings of blueness and despair along with confusion and feelings of success. there's lots of variation as to what kind of medical assistance and support people receive. some, like me, have been given really great support, while others seem to be left on their own to figure things out, which would be horrible. group members help where they can and try not to judge. it is very clear from the range of issues and behaviours that diabetes does not affect everyone the same way; foods that spike blood sugar levels for some, have no affect on others. or vice versa. i find it very helpful to learn these things and to share knowledge and commiseration with others. someone newly diagnosed asked us to share our routines. this is mine... 4:45 a.m. wake up and scan with the Freestyle Libre 2 flash glucose monitor (i have a free sam
navigating diabetes from diagnosis to...eternity? we'll see. I'm in my late 50s. i have no colon. i'm a polyamorous pansexual feminist writer, editor, visual poet and publisher living in Ottawa, Ontario, Canada. I approach all things in my life with ferocity. I like to explore and learn, make connections with others. I almost died, so I'm so grateful to still be here. I will be honest and candid, stirring up shit at times (ironic for a colon-free human). Oh, I also make a lot of puns. Stay Tuned