Patient advocacy organizations are a highly influential voice in the healthcare system, providing a critical link to real-world patient experiences. Armed with a deep understanding of what it is like to live with chronic conditions such as multiple sclerosis (MS), hemophilia or one of the conditions currently under research by Biogenscientists, patient advocacy organizations help us better understand unmet patient needs, shape our discovery and development programs and enhance our treatments and patient outcomes.

These organizations help us learn about the needs of the community and the challenges patients, their families, support systems and healthcare providers, face. This knowledge enables us to develop collaborative programs that support patients and their care partners.