Amid evolving health care policies, the American Epilepsy Society reaffirms its unwavering commitment to advancing health equity for people with epilepsy and fostering an inclusive, supportive environment for epilepsy professionals in research and clinical care. Every individual with epilepsy deserves the opportunity to attain their highest level of health, free from stigma and barriers to care. We take seriously our responsibility to make this vision a reality by advancing research, education, and clinical practice.
We are committed to these principles:
- Championing evidence-based science by ensuring that clinical decisions and public health policies are grounded in rigorous, evidence-based science. We support public health professionals and advocate for actions that are made in the best interests of patients.
- Promoting health equity by using our collective AES voice—in partnership with policymakers and other medical, research, and patient organizations—to ensure all individuals with epilepsy have access to care and resources, regardless of socio-political changes.
- Fostering collaboration and community through strengthening partnerships across disciplines and sectors, cultivating a united community with a shared purpose of improving outcomes for people with epilepsy.
Over the past year, we have prioritized and strengthened our dedication to health equity and inclusion in epilepsy. We will continue to expand our initiatives and are committed to driving meaningful progress for those working in epilepsy and the patients they serve.
As the national healthcare landscape continues to evolve, navigating these changes will demand vigilance and proactive leadership. We are committed to staying informed on policy developments, emerging trends, and issues that could impact our members and those living with epilepsy.
Our commitment is steadfast: we will champion inclusion, equity, and innovation--because the epilepsy community that we serve deserves nothing less.