Resources to support advocacy capacity building for people living with NCDs and other affected parties

Advocacy College

Our Patient Advocacy College is an educational program for patient advocates. In addition to the people most affected by NCDs, namely, people living with NCDs, their family members including bereaved family members, and their supporters, we hope this content will be utilized by anyone working together with these parties for solutions, such as politicians, administrative officers, healthcare providers, and people representing private companies. (Please note that this content is provided in Japanese only.)

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(Coming soon.)