I feel honoured to have three children with albinism
Stop insulting my three albino children in the street – they are my pride and joy
- Stacey Chappell, 34, from South Tyneside, is proud of her unique children
- Jay, 15, Leon-James, three, and Amelia Grace, one, are all affected
- READ MORE: Is this the world’s biggest albino family? British-Asian clan has FIFTEEN members with the condition
A mother who has three children with albinism says she is ‘blessed’ and bemoans ‘rude’ comments from the public.
Stacey Chappell, 34, a full-time mother, and her husband Jason, 40, a cleaner, from Hebburn, South Tyneside, did not know anything about albinism prior to their children’s diagnoses.
The condition affects the production of melanin, the pigment that colours the skin, hair and eyes, which gives Stacey’s children pale skin and visual impairments.
The mother-of-five said she wishes people would stop making ‘rude’ and ‘nasty’ comments as she and her husband feel ‘so blessed to have them’.
Albinism affects the family’s everyday life because the youngsters have to wear factor 50 sun cream every time they go outside, even when it is cloudy.
Stacey Chappell, 34, a full-time mother, and her husband Jason, 40, a cleaner, from Hebburn, South Tyneside, who has three children born with albinism say they are ‘blessed’ to have kids with the rare condition (L-R Stacey, Jason, Sky, Jay, and Lexi holding Leon-James)
The couple have also installed blackout curtains at home because sunlight can cause severe burns due to the reduced amount of melanin in their skin.
After the birth of their first child Jay, 15, Stacey said she ‘blamed herself’ for his albinism because ‘she made him’ and the couple were in and out of hospital ‘all the time’.
Stacey suffered with postnatal depression and initially rejected help from others, feeling it was ‘her responsibility’ to look after him.
However, the couple later made contact with Guide Dogs – the leading UK charity for people with sight loss – and this has been invaluable.
Despite the daily challenges the couple face, they said they feel ‘privileged’ to have three children with a ‘rare’ condition and they hope that by talking more openly about albinism, people will think twice before making ‘nasty’ comments.
Stacey said: ‘I feel privileged. I’m so blessed to have them because it’s a rare condition. We’re actually honoured to have them as our kids; they’re so rare.
Stacey said Jay (pictured) also suffers with anxiety and ‘lacks confidence’ as a result of his albinism, and he has been subjected to hurtful comments by his peers (Jay holding Amelia-Grace)
Stacey shared an adorable snap of Leon-James holding hands with his little sister Amelia-Grace
The condition affects the production of melanin, the pigment that colours the skin, hair and eyes, which gives Stacey’s children pale skin and visual impairments (pictured Leon-James, three)
Stacey’s daughter Amelia-Grace undergoing light therapy to treat jaundice – related to her albinism
Stacey and Jason Chappell’s son, Leon-James with his glasses on as he can only see at six metres
‘People will go, ”Look at his hair, look at his eyelashes”… and I’ll say, ”Yeah, he’s an albino”.
‘Then they’ll say, ”Why do you feel like you’ve got to tell people?”, and I’ll say, ”Do you know why? Because I’m so privileged; I feel so special having them as my kids”.’
Three of Stacey and Jason’s children – Jay, 15, Leon-James, three, and Amelia-Grace, one – were born with albinism and, as a result, all three wear glasses and have visual impairments.
The couple’s other two children – Sky, 13, and Lexi, 11 – do not have the condition.
Stacey and Jason had not heard of albinism before Jay was diagnosed at three-weeks-old, and they said they were told by doctors that they could not go abroad, they would need to install blackout curtains, and that he needed to wear sun cream any time he went outside.
Stacey said the information given to them at the time was limited, but they ‘got on with it’, doing everything they could to support Jay – and even today, they are still learning.
‘With him being our first child, it was a learning curve, but it was natural,’ Stacey said.
Stacey and Jason Chappell’s children (left to right) Sky holding Amelia-Grace, Lexi holding Leon-James, and Jay
The Chappell family had a festive day out as they visited santa last year at a Guide Dogs Christmas party (pictured Jay, 15, Sky, 13, and Lexi, 11, Leon-James, three, and Amelia-Grace, one)
The sibling are all very close to each other and Leon-James and his little sister Amelia-Grace have a special bond
‘I think it was more challenging when he started going to school – and that’s when we started figuring out, “Wow, this is totally different”.’
Jay is registered severely sight impaired; he has to use size 36 font and sometimes has trouble walking outside or crossing the road due to his reduced vision.
Stacey said different weather conditions – sun, rain, and snow – can affect Jay’s ability to identify buildings, cars and footpaths, and this has led to several accidents.
‘As he got older, as he got taller, he was having more and more accidents; he actually walked into buildings,’ Stacey said.
‘What we can see at 3,000 metres, he can only see at six metres.’
Stacey said Jay also suffers with anxiety and ‘lacks confidence’ as a result of his albinism, and he has been subjected to hurtful comments by his peers.
Amelia-Grace attends My Time to Play sessions set up by the charity, which help children with sight loss develop a broad range of skills through play
Leon-James is registered visually impaired and Stacey recalled another moment in a supermarket where a shopper made a ‘rude’, discriminatory remark
‘He is too shy, and because he’s had such bad things happening to him, he thinks everybody is going to be nasty,’ Stacey continued.
‘Trying to explain that not everybody is nasty, and people are there to help you, is so hard.’
Leon-James is registered visually impaired and Stacey recalled another moment in a supermarket where a shopper made a ‘rude’, discriminatory remark.
Stacey said: ‘We were actually in Iceland, and he nearly walked into this man, and he nearly walked into this lady.
‘He did it twice, so I apologised and said “sorry” and I didn’t say anything else, and she went: “No wonder he can’t see with those stupid glasses on”.’
Stacey pushed a lot of people away at first after Jay was born, and she said she felt guilty and responsible for her children’s albinism.
However, when Jay started going to school, the couple began receiving support from the local council’s visual impairment team and then Guide Dogs, which has been ‘amazing’.
When Jay started going to school, the couple began receiving support from the local council’s visual impairment team and then Guide Dogs, which has been ‘amazing’
Despite the daily challenges the couple face, they said they feel ‘privileged’ to have three children with a ‘rare’ condition and they hope that by talking more openly about albinism
What is albinism?
People with albinism often have white or very light blonde hair, although some have brown or ginger hair.
The reduced amount of melanin can also cause eye problems because melanin is involved in the development of the retina.
The 2 main types of albinism are:
- Oculocutaneous albinism (OCA) – the most common type, affecting the skin, hair and eyes
- Ocular albinism (OA) – a rarer type that mainly affects the eyes
Albinism is usually obvious from a baby’s appearance when they’re born.
Stacey and Jason have been supported by Guide Dogs for six years now, describing them as ‘like family’, and said they have helped to improve the family’s confidence.
Habilitation specialists have helped Jay use a cane to navigate independently, read large-print CustomEyes books, and master technology.
They have also helped Leon-James start day nursery and are currently supporting him through his transition to primary school.
Amelia-Grace attends My Time to Play sessions set up by the charity, which help children with sight loss develop a broad range of skills through play.
The sessions also allow Stacey and Jason to connect with other parents of children with visual impairments.
‘It’s so nice to actually chat to somebody who understands you and your child,’ Stacey said.
‘Nobody’s there to judge you, and sometimes you do feel like you’re judged.’
Stacey said it is easy to ‘take everything for granted’ and she feels many people are ‘ignorant’ to the challenges families may face, particularly when it comes to health conditions.
However, she hopes that, by speaking out about albinism, people will be more open-minded and want to help, rather than discourage and pass judgment.
‘You know that saying – ‘never ever judge a book by its cover’ – and I think just the way people look at other people,’ she said.
‘If people knew about that condition, even with any kind of visual impairment, or any other condition, then I think this world would be a lot different.’
Guide Dogs has recently launched its We Find the Way advert, which champions the My Life Skills service that Guide Dogs offers.
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