Parents move 3,000 miles away from home to protect albino babies from the sun


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Parents moved their family-of-nine almost 3,000 miles away from home to protect their albino toddlers from the sun.
Ally and Ryan McNallen decided to move their seven children from the desert to the mountains for the sake of their identical twin sons Aldridge and Argon, who are 18 months old.
The white-haired, fair-skinned twins were diagnosed with albinism in the summer of 2018, a condition in which their skin, hair and eyes lack melanin pigment.
The condition means the twins have vision abnormalities and their light skin is very susceptible to damage from the sun.
Mum-of-seven Ally, 31, and husband Ryan, 35, were worried about the childhood their youngest kids would have in Gilbert, Arizona, USA, where exposure to sunlight is high.

The twins in the bath together (Picture: theblackandwhiteblog.com / SWNS)The parents made the decision to relocate 2,900 miles away to Presque Isle, Maine, USA, a moderate UV zone, with their seven children in tow.
Ally said: ‘When we found out the twins had albinism we wanted them to have a good childhood that wasn’t limited.
‘In Arizona, the UV index is so high.
‘My husband and I work from home so moving jobs wasn’t an issue and we just thought Maine would be a nicer life for our kids with special needs.
‘It’s been a big difference. The winter here is brutal.
‘Right now it’s summer so I just try to protect the boys in SPF clothing, hats and sunglasses when they’re outside. And I limit their outside time to 45 minutes.
‘In Maine I don’t have to worry about them as much as I would have to do in Arizona.’

Maliah, eleven, Addison, seven, Nolan, six, Emmeline, four, and Benton, two, Alridge and Argon (Picture: theblackandwhiteblog.com / SWNS)The twins were diagnosed with albinism when they were seven months old after they began suffering from nystagmus, a condition in which the eyes make repetitive, uncontrolled movements.
When an optometrist noticed the lack of pigment in their eyes during an exam, the twins underwent genetic testing which confirmed a diagnosis of oculocutaneous albinism type 1B.
This means that the twins, born at 32 weeks, have a reduced level of melanin pigment in their eyes, skin and hair, rather than a complete absence.
Many people who live with albinism experience vision impairment, but mum Ally says they won’t be able to fully assess Aldridge and Argon until they can communicate better.
Ally said: ‘At 18 months they don’t have too many issues except with their eyes.
‘People with albinism often have blurry vision as they have an underdeveloped retina.
‘Pigment plays a big part in how our eyes handle light and people with Albinism don’t have that.
‘We won’t know the level of visual impairment that the twins have until they get a little older, but they still have nystagmus and their heads move in certain ways to try and see the clearest they can.’

Aren’t they cute? (Picture: theblackandwhiteblog.com / SWNS)As Aldridge and Argon were born at 32 weeks, the twins attend regular physical and occupational therapy to help them catch up on their milestones.
Although the twins are identical, Ally said Argon and Aldridge are very different when it comes to their personalities.
‘Aldridge just loves his brother and wants to cuddle with him all the time whereas Argon wants to play by himself,’ she said.
‘Right now they’re making sounds and they love playing with blocks. They’re starting to walk and navigate their vision.’
Ally and Ryan, who are also parents to Maliah, eleven, Addison, seven, Nolan, six, Emmeline, four, and Benton, two, said educating themselves about albinism has been a family journey.
Ally said: ‘We were open and transparent with our kids about the twins’ condition.
‘Our oldest is eleven and she went online and began to educate herself about albinism.
‘She was great at explaining it and breaking it down to our other kids.
‘Sometimes people tell me the twins have such beautiful eyes, that they are angelic and unique.

The family moved 3,000 miles away (Picture: theblackandwhiteblog.com / SWNS)‘A few weeks ago a little girl asked what was wrong with them. That was a great opportunity for my daughter to educate someone else about albinism.
‘I don’t find the questions upsetting. It’s an opportunity to raise awareness. It’s not something you see very often so it is natural to be curious.’
Ally said moving to Maine was the best decision for her family and hopes her twins will thrive in the mountainous state.
More: Parenting

Ally said: ‘I think about the twins and their future a lot and I just hope when they start school and grow that they will get all the support they need.
‘They are so beautiful and I want to do the best for them, which is why my husband and I chose to move our family here to Maine.
‘And so far, it’s going great.’
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