With your help, Epilepsy Foundation New England aims to improve the lives of individuals and families impacted by epilepsy and seizures. Together, we can offer those with epilepsy help for today, and hope for tomorrow.
Do you know someone with epilepsy? Would you know what to do if they had a seizure with you?
The 90-minute Seizure First Aid and…
We’re working to help those battling epilepsy from all corners of New England, and we’re always reaching out to those just starting their journey. That’s why we’re putting our knowledge, experience, and community to work for visitors at all stages of the battle against epilepsy.
Your involvement and advocacy on behalf of those battling epilepsy is crucial to our success, and we couldn't provide the services we do without your help. Whether you give a little or a lot, we always appreciate the support.
Our team of parents, patients, doctors, healthcare experts, researchers, and New Englanders all play a big role in our progress. Want to add your voice to the effort? Get involved and let’s put and end to epilepsy throughout New England, together.
Epilepsy Foundation New England (EFNE) is pleased to announce that our territory is expanding to include Vermont in January. EFNE will serve the approximately 7,000 people affected by epilepsy in VT, starting with support groups in Burlington, Rutland, and online; family and community education confere
Epilepsy Foundation New England has been selected as a $1.5 million grant recipient by the CDC’s National Center for Chronic Disease Prevention and Health Promotion. The grant supports the Foundation’s continued focus on strengthening the health system to improve epilepsy care; fostering connections between clinical services and community programs; and addressing social determinants of health to improve quality of life for people with epilepsy with the goal of improving their social environment.
This blog post was submitted by Sunovion Pharmaceuticals Inc.
#MyEpilepsyHero is proud to feature Cole and Katie, two amazing kids who started their own initiatives to help fellow kids with epilepsy.
This #MyEpilepsyHero post is published with the permission of Cole and Katie.