Join us for a panel discussion about enhancing interactions with the healthcare system and society through art. View the exhibit, "one, one thousand... Photographs by Debe Arlook" on display in the Fulginiti Pavilion lobby. PANEL DISCUSSION: Debe Arlook Photographer, Artist & Lori’s...
Join the LGS Foundation and DJ's Kara & Tayla for an LGS Virtual Valentine's Dance Party! Meet up with friends virtually for dancing and socializing! You might even make some new friends! Have some snacks and drinks ready. Dress Up...
Topic: Using Your Voice for your loved one with LGS How do you feel about advocacy? Are you stuck trying to communicate with the school, the doctor, and your community? Join our monthly support group as we share stories of...
Dad’s and our Male caregivers are the centers of the LGS Family. Join our exclusive support group for male caregivers and Dads as we talk, share and offer encouragement to each other along this LGS journey. Bring your favorite beverage and...
Living with LGS is a marathon, not a sprint. Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great. Not only do the needs...
“Rare Disease doesn’t come with a manual, it comes with a mother who never gives up!” Tune In – February 20 & 28, 2023 For A Special Segment Of Behind The Mystery Featuring LGS Foundation Executive Director, Tracy Dixon-Salazar, PhD ...