Patient and caregiver perspectives inspire our work—from our study design to our internal culture. Identifying unmet patient needs drives our research and development focus. This patient-centricity keeps everyone grounded in our purpose—to help improve the well-being of patients, caregivers and families impacted by CNS diseases, including Postpartum Depression and Major Depressive Disorder.
- Postpartum depression (PPD) is the most common medical complication of childbirth. In the US, estimates of new mothers identified with PPD each year vary by state from 8% to 20% with an overall average of 11.5%.
- Depression is a leading cause of disability worldwide. More than 300 million people worldwide are now living with depression, an increase of 18% between 2005 and 2015.
Feelings of guilt, shame, or fear associated with these disorders can keep sufferers from speaking up and getting care. At Sage, we believe this must change.
We are committed to partnering with the advocacy groups as they strive to reduce suffering and improve quality of life for all who suffer by breaking the stigma associated with mental illness, increasing symptom awareness and diagnosis, and supporting patients in navigating pathways to care.
Our Patient Advocacy team is committed to developing transparent and long-term relationships with advocacy groups that serve the CNS community. These groups are vital, independent patient champions, and we aim to learn from and collaborate with them as we pursue our shared goals.
We hold ourselves accountable for acting with a sense of urgency to help reduce barriers to disease recognition and management. We do this by supporting efforts to:
- Raise awareness of the burden of CNS disorders
- Increase early diagnosis and close gaps in care
- Help patients navigate access to medicines and healthcare services
To learn more about our patient advocacy efforts, email firstname.lastname@example.org