Student living with type 2 diabetes and IDF Young Leader in Diabetes

I was diagnosed with type 2 diabetes at the age of 19, during my second year in university. Looking back on my high school years, and even in university, there was a lack of regular and understandable information about diabetes. I learned about the types of diabetes when I was in the 9th grade, and before that, I got basic knowledge of the condition from family members who lived with it. That was five years before my diagnosis.

I had a friend living with type 1 diabetes, who knew what to do and had told her friends. They were understanding and had an idea of what to do if something happened. I cannot say as much for school staff, but they were friendly and helpful and looked out for their students.

I did the same as my friend when I was diagnosed. I told my friends first and then my lecturers and other staff members. They were very understanding and curious to know more about my experience.

I think the KiDS programme would have definitely changed my whole diabetes journey. It would improve the way people see, hear and know about the condition. It should be compulsory in schools, especially if you have a family history of diabetes. Preparing those who are more at risk and keeping at least one family member informed will make a difference.