I had noticed for quite some time that something wasn’t right. I was always thirsty, tired, and even fell asleep in class. Of course I've wondered how I managed to get this disease. But there's no answer, and I just needed to accept it.
With the insulin pump I have more or less everything under control – at work and while doing sports. I play football and ski in the winter. That's really important for me, and I want to do sports just like everyone else. And I can do it.
The first year I still had major fluctuations, and although I had a good doctor who did a really good job explaining things, it took me a whole year to understand it and get used to it. I'm very open about my condition now and want people around me to be aware of it. I definitively plan on having a family one day – why shouldn't I?

I think we've got a high level of technology as it is, but maybe one day there'll be a medication you can just take and then that's it. I'm very optimistic about that. Yes, I drink alcohol when I go out, but I do notice the difference in my blood glucose levels the next morning. I can eat practically anything. Sometimes I have to experiment a bit because of the insulin, but it's mostly fine.

Stéphane’s father: The first year was difficult for him and for us because he had to inject himself with insulin several times a day. The pump is excellent. Everything has become so much easier. I wish for Stéphane a normal life and no problems due to his condition. I also hope he'll be surrounded by friends who will accept him the way he is.

Our advice to you: Don’t go looking for reasons, but just accept the way it is. In my opinion that's
very important.