Mariam Petrosyan, a 26-year-old woman, and Taron Petrosyan, her 28-year-old husband, both hailing from the enchanting city of Yerevan, Armenia, were filled with immense joy and excitement as they eagerly awaited the arrival of their precious 𝑏𝑎𝑏𝑦 boy.

With hearts brimming with anticipation, the couple’s dreams of parenthood finally came true when their son, Artyom Petrosyan, made his grand entrance into the world. However, their elation was accompanied by a bittersweet revelation when they discovered a unique feature adorning their little one’s body.

Artyom was 𝐛𝐨𝐫𝐧 with a captivating 𝐛𝐢𝐫𝐭𝐡mark, a rare and striking nevus condition that remarkably covered 80% of his delicate skin. The 𝐛𝐢𝐫𝐭𝐡mark presented itself as dark, raised, and oval patches, casting a mesmerizing pattern over his body.

In the face of this extraordinary occurrence, Mariam and Taron found themselves embracing their son’s distinctive beauty with boundless love and tender care, cherishing the exceptional journey they would embark upon with their remarkable 𝘤𝘩𝘪𝘭𝘥.

Artyom Aristakesyan was 𝐛𝐨𝐫𝐧 with nevus 𝐛𝐢𝐫𝐭𝐡marks of oval patches of raised, dark-coloured skin and also needed surgery for spina bifida.

Artyom Petrosyan is now at home with his family Credit: MDWfeatures / @𝑏𝑎𝑏𝑦.boypa

The youngster was 𝐛𝐨𝐫𝐧 with nevus 𝐛𝐢𝐫𝐭𝐡marks on 80 per cent of his bodyCredit: MDWfeatures / @𝑏𝑎𝑏𝑦.boypanda

His 𝐛𝐢𝐫𝐭𝐡marks are an indication that his body is struggling to create melanin and pose a threat of becoming cancerous in later life.

Mariam Petrosyan, 26, and 28-year-old dad Taron, from Yerevan, Armenia were warned by doctors they didn’t know how long Artyom would live due to the highly increased risk of skin cancer.

But both were left horrified when doctors told them they could leave him behind if they didn’t think they would be able to take care of him at home.

“We only found out about Artyom’s nevus 𝐛𝐢𝐫𝐭𝐡marks when he was 𝐛𝐨𝐫𝐧. I was completely shocked,” Mariam said.

“The doctors had never seen nevus marks like Artyom’s before and they soon realised he also had spina bifida.

“It was all such a blur. They took him away for a ninety-minute surgery to correct his spine and it took five days of recovery before we could properly see him again.”

Little Artyom with his mum and brothers Credit: MDWfeatures / @𝑏𝑎𝑏𝑦.boypanda

Doctors had even told Mariam and Taron that they didn’t have to take Artyom home with them after he was 𝐛𝐨𝐫𝐧.

“I remember them sitting us down. Artyom hadn’t opened his eyes yet and they told us he might never open them due to the nevus 𝐛𝐢𝐫𝐭𝐡marks in that area,” said Mariam.

“They also said they didn’t know how long he’d live for and that if we wanted to, we could refuse to bring him home because taking care of him would be too hard – we didn’t listen.

“Me and my husband finally got to walk into Artyom’s ward. I was nervous.

“My husband called Artyom’s name and we saw him stir – then I called his name and he opened his eyes.”

Artyom underwent surgery for spina bifida after he was 𝐛𝐨𝐫𝐧Credit: MDWfeatures / @𝑏𝑎𝑏𝑦.boypand

Doctors have warned he is at risk of skin cancer Credit: MDWfeatures / @𝑏𝑎𝑏𝑦.boypanda

Artyom’s brothers, Narek, three, and Artur, two asked Mariam why Artyom “had chocolate dabbed on his face”

But after learning about their brother’s condition, they’ve done nothing but protect their youngest sibling.

Mariam says Artyom occasionally receives the odd stare, but others have deemed him to be ‘a gift from God.’

Nevus 𝐛𝐢𝐫𝐭𝐡marks can be removed but it’s rare that they cover 80 per cent of the body as they do in Artyom’s case. He even has nevus 𝐛𝐢𝐫𝐭𝐡marks on his brain which cause occasional seizures.

“Most people are shocked when they see Artyom – some smile at him. Someone also told me he was a gift from God.

Soυrce: lifeaniмal