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Powerful Photo Series Highlights The Experiences Of Those Who Live With A Rare Disease

An authentic photograph sequence is highlighting the wonder in folks with uncommon illnesses and their caregivers. 

Welsh photographer Ceridwen Hughes created the Beauty of Rare mission, which options 16 individuals who have a unprecedented situation or love any individual who does. The sequence is an initiative of Same however Different, a group group aimed toward elevating consciousness and counteracting prejudice in the case of folks with disabilities. 

Eddie Has Infantile Spasms


Ceridwen Hughes

“When you have a child with special needs, you pretty rapidly become aware that when someone asks you about them, you should never start with their disabilities, but there’s no denying it. That’s the focus of your attention. … Eddie’s a boy who is seriously held back by his condition. I suppose in a way, I don’t entirely know who he is because of the fact he’s not developing, and that’s pretty much because of the seizures.”

“I wanted to capture elements of the participants’ personality whilst including curious elements that relate to their rare disease or situation,” Hughes informed HuffPost.

“For example, in Jack’s photo, there are tins of spinach, as people often associate that with Popeye and his huge strength and large muscles,” she defined. “Children affected by Duchenne muscular dystrophy, as Jack is, often have larger calf muscles that would lead you to think they are very strong, and yet this is actually a sign that the muscle is degrading and they become weaker.”

Meliz Has Beta Thalassaemia Major


Ceridwen Hughes

“One of the toughest facets of the situation for me is the tiredness. My again additionally occasionally throbs on account of the place the bone marrow is making an attempt to provide extra blood cells when I’m because of have a transfusion.”

The mission took over 18 months to finish as Hughes contacted households suffering from prerequisites like hypophosphatasia and Ehlers-Danlos syndrome and attached with uncommon illness toughen organizations to succeed in out to folks on her behalf. The photograph shoots happened at 3 places in North Wales, and he or she additionally recorded video interviews with the members. 

“When we were discussing the plans for the images with each family, we were at times nervous, as we had to discuss very emotional issues,” mentioned Hughes. “In one of the images the mother is holding a clock with the hands nearly at midnight, which represented doomsday. Without treatment, her child will die, so research is critical, and yet time is running out. Topics like this can be difficult to discuss but even harder to see in such a visual way.”

Jack Has Duchenne Muscular Dystrophy


Ceridwen Hughes

“He looks healthy, but that’s the heartbreaking thing, because at the end of the day, his muscles are wasting away and he is dying.”

The photographer mentioned the collaborating households appreciated the overall pictures very a lot. One player, Toni Mathieson, whose youngsters had Niemann-Pick illness shared her reaction: “If people have a greater understanding of the impact of rare diseases and can identify with those affected, they won’t be perceived as being different.”

Mathieson’s response to the footage captures what Hughes needs all audience to get out of the sequence. 

Lizzie Is 1 Of three Siblings With Huntington’s Disease


Ceridwen Hughes

“She has deteriorated a lot quicker than [her brother] Christopher and has gone from a bouncy, dancing beautiful girl to being unable to speak, doubly incontinent and unable to walk. It is a terrible, terrible disease. … All Lizzie ever wanted was children. She just wanted a nice house and children. Four children she wanted, and she would have made an amazing mum.”

“We hope that when people see the images, they are curious to know more and by learning about those affected, it will highlight that, whilst they may be affected by a rare disease, they are still people just like you and me who have feelings, dreams and hopes for the future,” mentioned the photographer. “Ultimately, we are all the same but different.”

Keep scrolling to look Hughes’ footage and skim the topics’ tales, and consult with the Same however Different web page for a closer take a look at the members and their prerequisites.

  • Lizzie’s Brother Jonathan Also Has Huntington’s Disease

    Ceridwen Hughes

    “I used to run nearly every day and have completed marathons, but because of the way my condition has affected me, I have had to give it up. I have also had to finish work because I fell a few times. It was really, really hard at first because it meant I had so much time to think, but I have started doing charity work to raise awareness of Huntington’s disease, and so that is keeping me busy. … The worst part of the condition? The end, probably. Seeing my sister and my brother and the way it has affected them. But at this point, I’m just trying to be positive. That’s all I’ve ever done.”

  • Vinnie Has Spinal Muscular Atrophy Type 1

    Ceridwen Hughes

    “Strangely, his diagnosis has changed me as a person, for the better, most definitely. You learn to appreciate things that you took for granted before, like just spending time together. You really cherish those silly little things and all the things like the materialistic stuff that you were bothered about before really aren’t important. … Everyone deserves the right to live and to live a full life, and these are bright, intelligent people who need a chance. This is the biggest genetic killer of children under 2 years of age, so these perfectly bright, able children that just want to be children are dying. Some are also not getting the correct standards of care because doctors don’t think their life’s worth living. Just because they can’t move doesn’t mean they don’t have an amazing quality of life, because all a child needs is love. That’s all they need.”

  • Barbara Has Progressive Multiple Sclerosis

    Ceridwen Hughes

    “MS is invisible, except for when I appear drunk and lose my balance.  Because there are no obvious outward signs, people assume the worst. They also don’t understand the symptoms I experience, the constant tingling and discomfort I get throughout my whole body — far worse when I am tired, sometimes preventing me getting to sleep. It’s invisible, and people just don’t get it. I do appreciate that it’s very hard to understand and have pretty much stopped trying to explain.”

  • Toni’s 3 Children Had Niemann-Pick Disease

    Ceridwen Hughes

    “Hannah and Sam passed away in 2004 and Lucy in 2007. … I didn’t want anyone’s pity, and I still feel I don’t need it. … If someone says to me, ‘Have you got children?’ and then I tell them our story, I can see pity in their eyes. I don’t want that. I want them to listen and understand that I am very grateful for the experiences I’ve had and the time that we had with our children.”

  • Lucy Has Ehlers-Danlos Syndrome Type 3

    Ceridwen Hughes

    “I am hypermobile. It is a soft-tissue connective disorder, which can affect anywhere in the body. Because it’s a collagen deficiency as well, it can affect anywhere in your body, from your brain to veins or even your heart. … If I could tell people one thing, it would be that having a rare disease does not make you a weirdo. We’re just as normal as you. We just have a few quirks. … I just want people to treat me normally and accept our differences.”

  • Maddox Has A Perinatal Form Of Hypophosphatasia

    Ceridwen Hughes

    “It’s so important that we raise awareness of rare disease as a whole, but particularly for us, hypophosphatasia is an ultrarare disease, because if people don’t know about it, these children might not make it. … We couldn’t believe as a family that there was even a study going on about such a rare condition as hypophosphatasia. We feel really lucky that we were in the right place at the right time and we had access to the drug for Maddox, because without it, he wouldn’t be here now.”

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