Support Vitiliglory
The Beginning
Our founder, Ferrat Destine, was diagnosed with vitiligo at a young age. Growing up, he faced many challenges, including misunderstanding and rejection from society. However, these experiences only fueled his determination to create a platform where people with vitiligo could find support and acceptance.
The Turning Point
In 2024, Ferrat decided to share his story more openly, using social media and public speaking to raise awareness about vitiligo. The overwhelming positive response he received led to the creation of Vitiliglory.
Building a Community
Vitiliglory started as a small project but quickly grew into a vibrant community of individuals who share their stories, support one another, and spread awareness. Our community is a testament to the strength and resilience of those living with vitiligo.
Looking Ahead
We continue to expand our reach, offering educational resources, support groups, and public events. Our goal is to ensure that no one with vitiligo feels alone or misunderstood.