Former Judo Champion Shares Personal Journey with Vitiligo
Yehali Lavi, a former Israeli Judo champion, has shared his personal experience growing up with vitiligo, a condition causing skin depigmentation, to raise awareness and support for others affected by it. Lavi was diagnosed at age five and recalls the intense self-consciousness and bullying he faced, including peers who feared contagion and made hurtful comments. His father would even color his skin to hide a patch behind his head, a practice Lavi now finds unfathomable.
The challenges were amplified in his youth, particularly in judo, where he felt exposed on the mat. He recounts an incident in fourth grade where the fear of onlookers' stares prevented him from competing in the Israeli championship. Despite these struggles, Lavi eventually returned to the sport, winning the Israeli championship twice and achieving seventh place in Europe.
However, Lavi emphasizes that his most significant victory was overcoming his shame and learning to accept himself. He acknowledges that the condition still occupies his thoughts, especially in new social situations, but he has developed coping mechanisms over time. He now advocates for greater sensitivity and understanding from the public, particularly from parents of children without vitiligo.
Lavi urges parents to educate their children about vitiligo, explaining that it is not contagious and that there is no reason to fear or avoid interacting with those who have it. He stresses the importance of teaching children how to ask questions respectfully, distinguishing between natural curiosity and mockery. He founded 'My Seal,' an Israeli vitiligo association, to provide support and community for individuals and families affected by the condition.
The association will host its first conference on October 15th at Ichilov Hospital. Lavi views this event as a major triumph, symbolizing a community coming together and a step towards a more accepting reality for children diagnosed with vitiligo today. He hopes this initiative will foster a larger community and provide a sense of belonging for those with the condition.
