Wow, you were diagnosed pretty late huh? Guess your pancreas wasn't ready to give up the ghost too early!
I think my body totally rejected itself once I stopped track and field
Seriously, I suppose I was older than most, but it was really slow onset (latent autoimmune diabetes in adults). I knew it was coming so I had lots of time to prepare for the point in time where I would be injecting. In a way, that was good ... but I felt like my body was a time bomb. I didn't know which day I'd wake up and finally be insulin dependent. In the interim, I was never given oral medication. I just changed my diet.
Technically, I have Type 1.5 diabetes, not Type 1, but most people don't know what Type 1.5 is, so it's easier to just say "Type 1"
EDIT: I should state that I'm a nightmare as a patient. I'm stubborn and I prefer my treatment to be self-directed
![Big grin :D :D](data:image/gif;base64,R0lGODlhAQABAIAAAAAAAP///yH5BAEAAAAALAAAAAABAAEAAAIBRAA7)
At the time I was diagnosed, the endocrinologist thought I had Type 2, even though he said I didn't fit the profile. He suggested that I start oral medication, but I said "NO", mostly because if I didn't fit the profile, and my test results were mostly negative for Type 2, why would I start oral meds? He kind of agreed with me, but said I needed to have blood tests done every 3-4 weeks, and a glucose tolerance test done every month.
Needless to say, when I was diagnosed, medical science certainly wasn't what it is today.