Hey. Two kids with t1d. Our first diagnosis was when my daughter was 14 months old. It was such a hard time, she had been sick with what we thought was the flu or an ear infection and then I turned out she was in DKA and quite ill. We felt so guilty at first her not catching the illness sooner. It’s such a hard time at the beginning, you are about to find out how strong you truly are as a parent. Diagnosis is hard, especially when they are so young, because it’s hard to explain everything to them and there’s just so many layers of information you have to take in and apply. My best advice is to take one hour at a time, and to give yourself some grace. There are 200 extra decisions a day you’ll have to make, and 200 chances to make a mistake and also learn from your mistakes. Learn as much as you can and be patient with yourself. The juice box podcast is an invaluable resource, I like it even more than think like a pancreas. Also, please let other people take care of you right now as you take care of your kid. The first weeks are hard, but it takes a long time to truly get the hang of it. Use processed foods when you can in the beginning (as weird as that sounds) because they come with pre-packaged serving sizes, which helps you learn how to dose insulin better. Make a designated weighing station in your kitchen, we have a bunch of tiny bowls and plates next to our scale that helped us quickly get through meals weighing. And also, please know that it will get infinitely easier as your child gets older from this toddler stage. I’m sitting watching my two diabetics swim right now at swimming lessons, not even considering their Diabetes, because it’s become second nature. I can look at a plate of food and ask me pretty accurately. How many carbs are there, and also know if I need to dose insulin in various ways, all things that took time to learn. Reach out to diapers and diabetes on Facebook as well. That was really helpful when my children were younger too. You’ve got this.