Moment baby born blind sees city lights for first time after eye surgeryMoment baby born blind sees city lights for first time after eye surgery

To view this video please enable JavaScript, and consider upgrading to a web
browser that
supports HTML5
video

Up Next

Violet Paul, a one-year-old girl, has known nothing but darkness.

She was born with a rare gene, FOXC1, which means she has no irises, high eye pressure and experiences jittery eye movement.

Irisis, the colorful ring in our eyes, aren’t just for show. They control how big or small our pupils are, which lets light through.

Without them, Violet’s eyes are completely black and let too much light through, a condition called Aniridia.

Parents Madison Mitchell, 24, and Steven Paul, 30, considered everything they could to help, with doctors saying she’d be lucky to see a ceiling light.

But at just two weeks old, Violet underwent trabeculectomy surgery at the University of Iowa.

Steven, Madison and their daughter Violet (Picture: Madison Mitchell/SWNS)

The operation, often carried out on people with glaucoma, involves draining fluid from the eye.

The treatment was a success, introducing a child who has barely seen anything to a world of light.

Violet has slowly begun to see for the first time, with the family celebrating by taking her on a nighttime stroll through St. Louis, Missouri, on April 6.

In a video posted to Madison’s TikTok account, Violet can be seen gazing upwards and smiling at the streetlights as her dad carries her.

Madison, a stay-at-home mum from the Midwest, said: ‘She was so happy and awestruck that she began kicking her feet, squealing happily, smiling, and shaking her head out of happiness.

Violet was born without irises, so her eyes are sensitive to even dim light (Picture: Madison Mitchell/SWNS)

‘It’s a moment Violet’s father and I will cherish forever. It’s bigger than taking her out at day because she’s sensitive to the sun.

‘It was such a reassuring moment where we both knew as her parents that we were doing right by our daughter in trusting her team of doctors and making sure to follow her treatment plan.’

Madison regularly posts about Violet on social media to raise awareness of the rare condition Violet has, Aniridia.

Around one in 50,000 people are born with Aniridia, according to Sight Research UK.

Sponsored

Violet also has congenital glaucoma, where the optic nerve – the tissue that transmits what the eye sees to the brain – is damaged by high pressure.

This clouded her corneas, which focus light on the retina at the back of the eye, before she was born.

@madison_mitchell02

If you would have told me last July that we would be taking Violet on a carribean cruise. I would’ve told you that you’re insane. Like seriously. Insane. Violet used to be so sensitive to light that we couldn’t even have the ceiling lights on in our home. Let alone try to go outside with her. We were looking at multiple surgeries, a cornea transplant, and told that we would be lucky if Violet had enough vision to see lights. To be where we are today (just 9 months later) is the biggest answered prayer. Her glaucoma has been under control since her first and ONLY surgery and her vision is the best it can be without having irises. Her doctors have told us that it’s not often they get to be surprised in this way with their patient’s. We are forever grateful to be raising a living miracle and will never stop sharing her story. 💜 #Violet #aniridia #congenitalglaucoma #familyvacation #babysfirstvacation

♬ Cinema – 𝐂𝐚𝐫𝐫𝐢𝐞☘𝐋𝐲𝐫𝐢𝐜𝐬

Violet celebrated her first birthday on July 4 – even watching a fireworks display, something doctors thought she would never see.

‘It was hard not to get emotional watching Violet be enamoured by fireworks,’ Madison wrote on TikTok, sharing photos from the show.

‘Knowing that she is truly seeing them brings me unexplainable joy.

‘Being Violet’s mom has made me appreciate all of life’s joy more than I ever did before. And for that, I am forever grateful.’

What is FOXC1?

Researchers have tied crinkles with the FOXC1 gene to dozens of eye-related conditions.

Mfazo Hove, a consultant surgeon in ophthalmology, or the treatment of eye diseases, told Metro: ‘When FOXC1 does not function normally, the front of the eye may not develop as it should before birth.’

‘Some children are born with abnormalities of the iris or the eye’s drainage channels.

‘The biggest concern is glaucoma because, if the drainage system is underdeveloped, pressure inside the eye can rise and gradually damage the optic nerve.’

Hove, of Blue Fin Vision, said it can cause photophobia, or light sensitivity, as well as reduced vision and glare.

‘The good news is that with regular monitoring, modern glaucoma treatments and appropriate visual rehabilitation, many people retain useful vision throughout their lives.

‘Genes like FOXC1 don’t determine someone’s future, but they do tell us who needs careful lifelong monitoring so we can protect vision before damage occurs.’

Get in touch with our news team by emailing us at webnews@usnewsrank.com.

For more stories like this, check our news page.


Discover more from USNewsRank

Subscribe to get the latest posts sent to your email.

0 0 votes
Article Rating
Subscribe
Notify of
guest
0 Comments
Oldest
Newest Most Voted
Inline Feedbacks
View all comments

0
Would love your thoughts, please comment.x
()
x