News & Upates

From iconic Mumbai facades to digital cinema, at Fragile X Society India, we led a historic nationwide campaign to bring genetic health, Fragile X Syndrome awareness, and early diagnosis into the light. All of India Lit Up in Teal Green On July 22, 2026, the night sky...

Cinema possesses a rare ability to transform abstract medical definitions into deeply felt human stories. Where brochures and clinical terms often fail to convey the daily texture of living with a rare condition, a well-crafted film can step in, replacing clinical...

There is an unspoken rule deeply embedded in the cultural fabric of India: family comes before everything, and caregiving is an unconditional, lifelong duty. When a child is diagnosed with a developmental or genetic condition, Indian parents step into the role of...

If you walk into a school, an urban pediatric clinic, or scroll through corporate wellness webinars in metropolitan India today, you will notice a massive, welcome shift. The word neurodiversity is finally shedding its status as an obscure medical term and entering...

In India, parents concerned about their child’s developmental pace are frequently met with well-meaning but passive advice. Phrases like "He’ll catch up eventually" or "She’s just shy" are common refrains from extended family and neighbors. While it is true that every...

For families searching for answers regarding a loved one’s unexplained developmental delays, navigating the medical landscape can feel overwhelming. Amidst the specialized terminology, "Fragile X" is a name that frequently flies under the radar. Despite being a...