Registration is Open for This International Lennox-Gastaut Syndrome Conference

Pack your bags LGS Warriors, your conference is headed to Orlando, FL this November!

The LGS Foundation is holding it’s fifth International Family and Professional Conference to promote collaboration between LGS families and professionals in order to share the past and future of LGS.

The LGS Foundation is a non-profit organization who strives to support those affected by LGS. While based in the US, they support people around the world. They provide monetary support for things like LGS services and research. To learn more about them, click here.

LGS is a rare form of childhood epilepsy, resulting in severe seizures. Additionally, there can be developmental delays, injuries from the seizures, and occasionally behavioral problems. While there are many potential causes, there are also many potential treatments available to help decrease the amount of seizures with hopes of little side effects and improved quality of life. There is no known cure. To learn more about LGS, click here.

Who: The LGS Foundation

What: LGS Foundation Family and Professional Conference

Where: Orlando, FL

When: November 10th through the 12th, 2017

To register for the event, click here.

Jessica Gladwell

Jessica Gladwell

Jessica Gladwell is one of PW's consultants and patient editors. She has lived with late-stage, chronic Lyme and POTS since circa 2002. She has also served as a caregiver to close family members with late-stage, chronic Lyme. Before diagnosis, she served as a business consultant for a large corporation and PM for a small digital branding agency. Now, she is proactive in the rare and neurological disease community, spreading awareness and advising on matters of health and lifestyle when living with a chronic illness.

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