I am curious. With all the shock and confusion involved in getting your diabetes under control, how should you be approached to participate in research studies? Some are only available to you during the first 10 weeks after diagnosis. Who should you hear from? Would any kind of brochure work amongst all the information that you receive? What could the doctor or nurse say to you to get you to participate, or are they too busy trying to teach you about diabetes?
Any comments would be appreciated!