Yes it is extremely unusual to be diagnosed so early - the doctors were very surprised. My diabetes nurse said she had only encountered one other person like me, and they too had been diagnosed during a medical for work. Because it is so rare, they cannot offer much information about how long the 'honeymoon' will last, so we are just playing it by ear really. My pancreas is still producing a significant amount of insulin.
I take a small dose of slow-acting insulin at night, and then fast-acting with breakfast and dinner. I just judge how much fast-acting insulin to take according to what I have eaten. Occasionally I misjudge it, and I often find that a dosage that was right for a certain meal on one occasion is not necessarily the right amount on another occasion!
Obviously like you I'd rather not have diabetes full stop - I meant I felt fortunate to be diagnosed at an early stage rather than later on!
Looking back the only symptoms I had experienced were very persistent thrush, and also taking a long time to recover from infections/illnesses. For example, about a year ago my sister and I both got a stomach bug at the same time - she recovered from it in three days whilst I had it for two weeks. - But obviously I never developed the full blown classic symptoms.
I am getting on fine with injections, and feel well-supported both by GP and the team at the hospital. I get the odd hypo - maybe two per week, but have so far not had any too severe. The lowest blood glucose reading I've had was 2.6 and I did feel pretty dizzy, but luckily so far I haven't had a disabling hypo or one which I couldn't treat myself.
The thing I most worry about is nighttime hypos. I try to avoid these by having a snack before bed when I take my slow-acting insulin, but I'm never sure what the best thing to eat is, and I hate eating last thing before bed. Any suggestions? I usually have an oatcake but am getting pretty sick of them now!!
When were you diagnosed Emma? I hope you're feeling much better now? How was Christmas?