India Illuminates Iconic Landmarks in Teal Green to Raise Awareness About Fragile X Syndrome
India lights up major landmarks in teal green for World Fragile X Awareness Day 2026 to highlight Fragile X Syndrome, the leading inherited single-gene cause of autism and intellectual disability. Fragile X Society India launches a nationwide campaign and releases the first Indian awareness short film "Fragile" to spread understanding and support.
Led by Fragile X Society India, the nationwide awareness campaign aims to bring Fragile X Syndrome out of public obscurity and create greater understanding about the genetic condition affecting individuals and families across the country. The campaign witnessed participation from corporate partners, medical institutions, and educational organizations, with several prominent locations displaying teal green lighting, awareness posters, educational standees, and community engagement activities.
The iconic Taj Mahal Tower in Mumbai was among the major landmarks illuminated on the occasion of World Fragile X Awareness Day 2026. Other participating locations included Planet Godrej and Breach Candy Hospital in Mumbai, City Centre New Town, Salt Lake Kolkata, and the Amrit Somani Memorial Center in Kolkata, The Connaught by IHCL SeleQtions in New Delhi, Apollo Children's Hospital in Chennai, WOW Crest by IHCL SeleQtions in Indore, Daiwik Hotels in Rameswaram, and educational institutions including The Cathedral and John Connon Senior School and Thomas House.
Alongside the landmark illumination initiative, Fragile X Society India has also introduced "Fragile", the first Indian short film dedicated to creating awareness about Fragile X Syndrome. The film highlights the emotional and diagnostic challenges faced by families navigating the condition and presents an accurate portrayal of their experiences.
The awareness film features prominent Indian actors including Rajniesh Duggall, Amruta Khanvilkar, and veteran actor Govvind Namdev, whose performances bring attention to a genetic disorder that remains widely misunderstood and frequently misdiagnosed.
"For over two decades, our absolute mission has been to ensure that no family walks this path in the dark," said Shalini Kedia, Chairperson and Founder of Fragile X Society India. "An accurate diagnosis does not just explain a child's present behavioral challenges; it fundamentally re-charts a family's reproductive future. By lighting up our country's proudest landmarks in teal green today, we are breaking the silence. We are building a nationwide system of support, recognition, and early medical intervention for the estimated 400,000 affected individuals across India."
Citizens across the country have been encouraged to participate in the movement by visiting illuminated landmarks, capturing photographs with teal green backgrounds, and sharing awareness messages through social platforms. People have also been encouraged to watch the short film "Fragile", share it with families and medical professionals, and support conversations around genetic health and autism awareness.
Fragile X Syndrome is a genetic condition associated with developmental delays, intellectual disabilities, learning difficulties, and behavioral characteristics that often overlap with autism. Due to limited awareness, many individuals across India remain undiagnosed or misdiagnosed, while many others remain unaware that they may carry the altered gene. Genetic testing and early clinical intervention can significantly improve outcomes for affected individuals and provide families with essential guidance.
Fragile X Society India, founded in 2003 by Shalini Kedia, is the country's leading support network for individuals and families affected by Fragile X Syndrome. The organization works as a bridge between families and the medical community by providing resources, guiding families toward accurate genetic testing, offering professional counseling, and building a supportive national network.
The nationwide teal green illumination campaign and the release of "Fragile" mark a significant step toward increasing awareness, encouraging early diagnosis, and ensuring that individuals affected by Fragile X Syndrome receive greater recognition, support, and medical assistance.

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