This same thought has also been bouncing around my skull. I got Type 1/LADA diabetes late in life ( I was 39 when diagnosed ) and struggled to find resources to understand my disease.
Since I was diagnosed at the ripe old age of 37, I hanker for an organization that focuses on adults with Type 1. Where is the place for us? Other than here on the Internet, of course? There is no non-profit, advocacy organization, or annual conference for us LADA types. Or for children with Type 1 who’ve grown up to be adults with Type 1, for that matter.