Two-year-old Vienna Shaw was born with a rare congenital melanocytic nevus (CMN) covering part of her forehead, a birthmark affecting roughly one in 20,000 newborns. Although doctors said it was not dangerous or cancerous, her parents worried about the emotional impact it could have as she grew older. After initially facing medical concerns and disagreement over whether the surgery was necessary, the family launched crowdfunding campaigns and raised tens of thousands of dollars to cover the treatment. Vienna eventually underwent surgery to remove the birthmark, leaving only a faint scar between her eyebrows, and her mother has continued sharing updates on her recovery as the little girl returns to everyday life.
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Two-year-old Vienna Shaw was born with a rare congenital melanocytic nevus (CMN) covering part of her forehead, a birthmark affecting roughly one in 20,000 newborns. Although doctors… <\/p>\n","protected":false},"author":1,"featured_media":6536,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"footnotes":""},"categories":[5],"tags":[],"class_list":["post-6535","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news"],"yoast_head":"\n