Stevie, a devoted mom, shares her family's journey after receiving the devastating news that her son had FOXG1 syndrome -- an extremely rare neurological genetic disorder. In this video, Stevie discusses how she and her family found hope and community in the FOXG1 Research Foundation and how the foundation is working to change the outlook for kids like Finn.
RESOURCES:
*FOXG1 Research Foundation:
foxg1research....
*Abilities in Action Pediatric Therapy (New Jersey):
www.abilitiesi...
*Hawkswood School (New Jersey):
www.hawkswoods...
RELATED CONTENT:
*A Family’s Story of Love & Resilience with FOXG1 Syndrome:
• Finding the Light: A F...
*A Teacher Empowering a Young Boy with FOXG1 Syndrome:
• A Teacher's Love: Empo...
@FOXG1Research #foxg1 #foxg1awareness #foxg1research #yourenotalone #yourstorycounts #shareyourstory #mediamoms
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14 окт 2024
