by CARLY FINDLAY
Rick Guidotti’s motto is “Change how you see. See how you change”. He does this through photographing people with genetic differences, just like he would photograph supermodels. The photos enable viewers to see the person, not the condition.
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by Rick Guidotti (Photo via the Positive Exposure Facebook page)
When Rick Guidotti was a fashion photographer, he was always told what was beautiful. He photographed the supermodels known by their first name only – Cindy, Claudia, Naomi, Christy. But he didn’t only see beauty on the covers of magazines.
In the late 1990s, Rick saw a beautiful girl outside of his New York apartment. She had long white hair and pale skin, radiating beauty. She had albinism. Rick did some research on albinism, looking at medical text books. He was heartbroken by what he saw – the people featured in the texts were just medical specimens – their eyes and genitals blocked out. They looked sad, sick, and Rick described them as “defined by their disease”.
They were not photographed to show their personality, they were photographed to show their condition. (When I was a child, I spent many hours in a cold hospital room being photographed for similar text books due to my skin condition which I’ve written about for Mamamia here.) He wanted to change the way people with albinism were represented in medical text books, as well as in media and society, and so he contacted the albinism association, asking if he could work in partnership with them, taking photographs for text books – “showing the world the beauty of albinism”.
At first the association was reluctant, concerned about sensationalism and exploitation. But then he put forward the idea of a genetic support group with the association, and suggested they could oversee his work.
His first photographic project was with a young girl called Christine – he said she was just beautiful, but afraid to hold her head up high. She had no self esteem as a result of being teased about her appearance every day. His studio was set up from the day before, when he photographed Cindy Crawford. He treated her just as he treated Cindy, holding up a mirror to her and convinced she was beautiful. He said that at the end of the session, she held her head up high, working the room, and had the confidence to change the way society viewed her. In 1998, Rick’s work was featured in Life Magazine, showcasing a range of people with albinism.
Since then, Rick has been helping many people feel more confident through sharing their lives through images, and for the world to “see the beauty in all differences”. He set up Positive Exposure with the view to change the way society views people with a wide range of genetic differences and medical conditions.
He attends medical conferences where he photographs people with many conditions. Although an artist, he demonstrates great fluency in medical terminology, and he told me that he picks this up through spending time at conferences and working in hospitals. He also holds exhibitions of his work – one is coming up in Grand Central Station, New York.
Rick had the ability to make me feel like I am the most important person in the world when he spoke to me. And it wasn’t just me who felt this – he had time for EVERYBODY he met at the festival, and he especially made those he photographed feel like a supermodel. Just like those supermodels are known by their fist name only, the people he photographs are known by their first name. And he is so passionate about his work.
He told me about the way showcasing external beauty in people with genetic differences helps individuals develop confidence. Positive Exposure has an equation: “Self acceptance = self awareness = self advocacy”. He said that one girl came to the realisation after a photo shoot that while society will always stare, the thing that has changed is that she no longer hates the way she looks.
Rick said “We need to come up with the opportunity for people to meet people like you through our photographs”. There is a perception in society, the media and the medical profession that people with genetic differences don’t want to be photographed, that we don’t want to stand out any more than we already do. That we don’t have a right to beauty, because our appearance defines us.
And while there is more to life than external beauty, it is a part of life, and people with differences have just as much right to feel and be told they’re beautiful as “everybody else”. it’s not about vanity or conforming to images on magazines. It’s being acknowledged for our beauty.
I have been asked why, when I am not keen on people staring at me, that I am so into fashion and love being photographed. It’s because I like to look the best I can. I heard Rick say “sometimes looking away is worse than staring”. Yes. It is. I see people in the street, busy in conversation, and then the catch a glimpse of me and look away in disgust. This hurts. When I dress up in something fabulous, I want people to look at me and think I am beautiful, not look at me in disgust.
Rick took some photographs of me. I was photographed with vaseline smears and scale in my scalp. But that’s ok – I was photographed as me. No airbrushing, no holding my tummy in. Just happiness, confidence and laughter.
He certainly made me feel like a supermodel, throwing in the “work its” and “slink over to mes”. He said, on a number of occasions, “see how beautiful you look Carly”. And I did. Rick gave me permission to shine.Through him photographing me, I felt beautiful, and proud to feel so. It is ok to want to feel beautiful, and want others to see you are beautiful, even when you don’t fit the traditional mould of beauty.
I asked Rick whether he believes someone with a genetic difference will be on the cover of Vogue magazine. He doesn’t think so, but he believes that the media needs to recognise that beauty is diverse. Magazines need to recognise the beauty in people with genetic differences.
I think I just met my hero.
More about Rick Guidotti’s project can be found at Positive Exposure.
Carly Findlay is a 20 something Melbourne woman working full time as an events planner/writer and a freelance writer on the side. You can follow her on twitter here or read her blog here.









Comments
35 Comments so far
Enjoyed your article, shared with me by a friend. My two young boys have Lamellar Ichthyosis. Keep up the great work!
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Great article Carly and beautiful pictures.
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There’s a clear difference between Ricks photos and the standard ‘supermodel’ shot – these guys are SMILING and look like people who might actually be fun to hang out with!
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I saw Rick speak at the festival and it was fantastic, someone from such a different background representing people with genetic differences in a positive way. Its great Carly that you wrote this article so more people can hear about his work
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Carly, I wish you could put your strength into words, or better still, a bottle. Does it come from your soul, from your parents love or is it just something within you? Physically, I was one of the ‘blessed.’ Born into a great family, educated at the best schools and physically beautiful. But something in me hated the attention and the attention of men, for no sane reaon, terrified me. I’ve eaten myself invisible and haven’t worn anything but grey or black for ten years. I just want to fade away. It’s not depression, I don’t think, it’s more that I simply don’t want to be seen.
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I had to keep looking to find out where the genetic differences were as I thought they all looked normal, so Rick, you’ve done a wonderful job or our lenses are changing towards difference:)
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Carly you are beautiful both inside and out. Thank you for your great post. Rick is doing an amazing thing and I am so happy there are people in the world like him trying to show that there is more than one type of beauty and more than one way of seeing people around us.
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Carly, you are incredibly beautiful. I’m so grateful to know you and that Rick made you see yourself as others see you has made him my hero too.
What an incredible man.
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Carly, wonderful article!!!! I am so happy to have met you, and count you as one of my dearest, and most fabulously dressed friends…xx
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what a fantastic idea and his photographs are stunning!
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Stunning Carly, just stunning.
M xx
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Oh, Carly! What a wonderful article you have written here. I would LOVE to meet this man someday. Do you think he would consider coming to our Dance-a-Thon in May 2013? There are going to be a ton of FIRST members there…dancing up a storm! He’d need to bring a camera with excellent shutter speed to catch all the great moves on the dance floor…..and joy on the faces!
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Hey everyone – thank you so much to Mamamia for having me again, and thank you so much for all the shares and comments. I’m so glad I got to tell you about the amazing Rick Guidotti. He really is changing the world, and I love how happy he makes people. If you get a chance to see him in America, or when he is back in Australia, please do. You won’t regret it.
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What a beautiful article to come across on a lazy sunday
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terrific article Carly- you write so beautifully. Thanks for making us aware of such a terrific project- I will share it with the families I work with (many children with genetic conditions). Great way to celebrate difference and beauty- how boring would the world be if we all looked like Cindy or Naomi!
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Not sure where my last comment went but wanted to let you know Carly what a great article I thought this was. Thank you for bring this fantastic initiative to my attention!
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Carly your posts always teach me something and/or expose me to something new. Thanks for such interesting content.
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Lovely photos, what a great idea.
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We met Rick through NOAH. We have been fortunate to see him speak and meet up with him at various functions. He is a great guy and so very full of positive energy!
(our son Hank is #8 in the images above)
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Hank is just beautiful!
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Those photographs are beautiful. Love, love love them!
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Thank you for sharing Carly, you do shine and you are beautiful.
An amazing story.
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I would prefer to see a photo of Carly with her stunning smile than a photo of a surly, no-personality model any day. These photos truly are quite beautiful.
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Thank you. This made my day.
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We were lucky enough to hear Rick speak at the Celebrating Diversity photographic exhibition in Brisbane in 2011. And then were thrilled when he held an impromptu photo session the next day with local families where my daughter was photograped by Rick. My daughter has Angelman Syndrome and is beautiful in every single way. I celebrate anyone who chooses to highlight this beauty to the rest of the world, he is dynamic and passionate about our gorgeous kids. Thank you Rick!
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Great article. However I disagree with this quote “There is a perception in society, the media and the medical profession that people with genetic differences don’t want to be photographed, that we don’t want to stand out any more than we already do. That we don’t have a right to beauty, because our appearance defines us.” I am in the medical profession and work with children with genetic differences every day. They are all beautiful, engaging and individual. The media and their portrayal of what is beautiful has a lot to answer for, but society – which society? And the medical profession – again a very broad group of people who cannot all be lumped together as having the same perception.
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Carly already knows how much I admire her. As a photographer, this article really struck home. This is using your power for good instead of the expected.
Made my day…AWESOME!

BB
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Amazing! Great post and love the video
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Wow what a fabulous guy, I loved everything about his clip. Thank you for sharing this inspiring work with us Carly. And, by the way you are gorgeous!
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What a beautiful story. Thank you so much for bringing a smile to my face in a time of depression.
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Carly, I want to put my hand up as one of those people who, if I caught a glimpse of you in the street, would probably quickly look away. And I want to make the point that it’s not from disgust. Not even a little bit.
Most of the time when I walk down the street I don’t think I really notice the people around me very much at all, but every now and then someone, for whatever reason, stands out as different, and without making a conscious decision my gaze has lingered. You say in this article that you are not keen at being stared at, it’s a sentiment I’ve heard many times before, one that makes perfect sense. That is why I look away, all the while mentally kicking myself. It’s because I’m hoping that you didn’t notice me notice. Because I don’t want to be one of the people who stared that day.
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You make me proud to be your friend Carly. I’m so glad you got to meet and work with Rick too. X
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Always love your stuff, Carly. This is awesome.
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This is beautiful. You made me cry before 9 on a Saturday morning!
I teach in a Special School, and I would love if more people could see how amazing and gorgeous the kids I teach are. People always tell me that they couldn’t do my job, how do I do it? They would feel too sad, or couldn’t handle it. Well, I love my job, I love the kids I teach, and look forward to going to work-and it’s all because of the kids. How many of them could say that?
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Thank you. I am the mother of a child who attends a school for children with special needs. My child is fabulous, and so are his classmates. His teacher is amazing. She believes in her students and works hard with them so that they can achieve. She cares about them and their families. We are blessed to have her.
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