Every two years, the LGS Foundation organizes a comprehensive multi-day educational meeting. The conference brings together more than 350 LGS family members and epilepsy professionals from around the world to better understand the causes, treatments, and how to live with LGS. Talks cover everything from treatment options to services and include information on improving quality of life, accessing resources, and much more.
In non-conference years, the LGS Foundation hosts the LGS Research Meeting of the Minds Conference for professionals and families and focuses on LGS research. We can’t wait to see you!
Thank you for Joining us for the 9th International Family & Professional Conference
More than 400 global leaders, healthcare professionals, family leaders, and advocates for LGS united in Phoenix, Arizona for three days of educational sessions and community collaboration, July 11-14, 2024.
“Our LGS Conference is more than an event – it’s a chance for us to strengthen bonds, share insights, and grow together as a community. Its success lies in the incredible spirit of our families, researchers, and partners coming together to learn, share, and inspire one another.”
– Tracy Dixon-Salazar, PhD, Executive Director
Conference Pictures
View Conference Photos on Facebook
Thank you to our Sponsors
We value our relationship with each of our partners. In addition to financial support, partners provide their unique expertise and perspectives on the issues and needs our families face daily. And while it is our commitment to improve the lives of those impacted by Lennox-Gastaut Syndrome that brings us together, it is our shared understanding that collaborative initiatives generate steadier progress and stronger outcomes that will ensure our partnership proves valuable for the families and providers in our community.
Interested in becoming a sponsor? Email us at info@LGSFoundation.org
Past LGS Family & Professional Conferences
LGS Foundation Family & Professional Conference June 17-19, 2022
Thank You For Joining Us
2022 conference sessions provided attendees with clinical and research updates on Lennox-Gastaut Syndrome, along with information on emerging therapies, special needs resources, and topics related to quality of life. This event allowed the opportunity to foster new relationships and collaborations, both for families and professionals. New this year was our Sib Camp and fun activities for those with LGS.
Please note that these photos are for personal use only. These photos are not authorized to be used for commercial purposes.
Updated 07/22/24 (KK)