#DeDoc° Session

For scientific and research centred events to allow a patient voice to be heard is a welcome development.

At ISPAD, #dedoc°, an international community by and for people with diabetes, held a session to get across what living with diabetes is really like.

Patient advocates are keen to influence the research agenda to ensure its relevance to the very people it is supposed to assist.

Advocacy Action – Does your government fund medical research, and if so how are patients involved in the process? Can you push for patient voices to be heard?

PDGN would like to thank EASD for registrations and a stall, and ISPAD for allowing us press access to the event.