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Undressing Disability

I'm judging New Blood Awards 2020

D&AD Awards – Creativity, Diversity and Durex

By Undressing Disability

D&AD, or the Design and Art Direction is an educational charity promoting excellence in creative advertising and design. Their New Blood Awards give applicants, often students, the chance to get ahead and gain the exposure they require to start or accelerate their creative careers. Each year, real, big name clients set the briefs for the awards, with 2020’s challenges being set by the BBC, Barclays, LEGO, Nike, Durex and Penguin amongst others.

Emily wears a stripey top, dungarees with a pattern of planets and sits in front of orange patterned wallpaper

We are delighted to say that Enhance the UK were asked to support Durex with their written brief and Emily, who leads our Undressing Disability Campaign, will be one of the judges. The Durex brief is based on:

‘fighting for diverse representation and empowerment in sex for disabled people.’

 

Judging Panel

Live judging starts today, Wednesday 3rd June, and we are delighted that a Durex is challenging sexual conventions. We’re also incredibly impressed with how many creative applicants have worked on this brief, read or watched our content and got in touch with us. It is essential that we remain impartial, so sorry that we couldn’t give any of you advice but we wish you the very best through these next judging stages!

The Awards

To find out more about D&AD, the amazing New Blood Awards, and the Durex brief, please visit: https://www.dandad.org/en/d-ad-new-blood-awards/ 

Our Undressing Disability Campaign

Read more about our Undressing Disability campaign and free Love Lounge advice service.

Follow the Undressing Disability campaign on social media. We’re @ETUKUndressing on twitter and @UndressingDisability on Instagram.

Charlotte Faragher smiles for the camera. She has long dark hair, a white top with blue stripes

Desirably Different by Charlotte Faragher

By Disability, Undressing Disability

What pitfalls feelings and experiences befall people considered different in our society?

How best should we tell our stories and attempt to turn negative perceptions on their head, or at least encourage discussion on these issues?

What role do mental health struggles, feminism, and body positivity have in permeating the current problems we face as well as promoting change?

My name is Charlotte Faragher and since September 2018 I have been advocating the exploration of these issues through my initiative, Desirably Different. Right now it is essentially a Facebook page where I post relevant media related content and thought pieces from stand up sets, to TED talks, as well as my own views in regards to these topics.

Desirably Different
I believe the media hold a special ability to often allow us to laugh at, reflect on and question our life as we see it. And also give us the opportunity to see what society might look like, in both positive and negative ways, if we don’t alter many negative pervasive views in society.

As the Undressing Disability campaign focuses on disability, sex and relationships, it is only fair that I should share some of my own experiences.

I have had quadriplegic cerebral palsy since birth and have had little romantic or sexual attention, even though I know it is something that my body wants and needs.

 

Even though my cerebral palsy hasn’t affected me mentally or academically, I do need a lot of help physically and explicitly from others just to live day to day. This can make pursuing potential romantic partners tricky. It can prove inconvenient to stay out late at night in my current family situation. A care company is employed most days to get me up in the morning and put me to bed at night to take the strain away from my parents. But as they come at specific times I have to be home earlier than I may want to be.

I consider myself to be a strong feminist and believe every person has the right to conduct their romantic and sexual lives as they choose, but I have never been open to using dating apps. My reasoning is twofold. Firstly, some people use the apps to look for casual sex which is not something I would enjoy. Secondly, like it or not I am a vulnerable adult and if I get myself in an uncomfortable situation I cannot walk away from it as easily as others. So there is a lot of risk there.

Charlotte Faragher smiles for the camera. She has long dark hair, a white top with blue stripes

I have been in love once. I was 17 and I fell for a guy who was one of the helpers on a Christian holiday for disabled young people. I could not deny my feelings for him no matter how hard I tried. Heartbreakingly for me, he had a girlfriend and did not feel the same.

As a consequence I started looking for love in unhealthy and risky ways- it was one of my darkest periods. I’m sure I am not the first person with a disability who has done this.

I think my desire to go to such lengths stems from my view that many disabled people still aren’t seen as sexually attractive or potential dating partners by the majority of people. And those who do like us in this way, people known as devotees, are currently forced to hide this side of themselves for fear of judgement and persecution. Education is key. I believe if more of these people felt comfortable enough to share testimonies without discernment, and the general public educated, this would have the potential to liberate many.

At my lowest points I often wonder.. Do I deserve romantic love at all?

My life is rarely simple and if I did date would I be able to treat a partner as they deserve? In both the physical and emotional senses despite my disability. But then I remember it is my human right to explore healthy romance and sexuality just like everyone else. I just need to try and drown out the voices that say I don’t deserve it. Or that I’m not good enough, hard as it may be.

I hope many who read this will start to think differently about disability and relationships as a result. We are a group with more to give than many realise. More people just need to have the courage to destroy harmful misconceptions and empower disabled people in positive ways.

Thanks to Charlotte for writing this brilliant article for us. You can connect with her at Desirably Different on Facebook.

If you enjoyed reading this please share it with your friends. Keep up to date with all our interviews, guest blogs and Love Lounge tips by joining us on twitter @ETUKUndressing or on Instagram @UndressingDisability.

 

Disabled Parenting podcast with Fran Hamilton and Enhance The UK

Disabled Parenting – A podcast with Fran Hamilton

By Disability, Undressing Disability

Fran Hamilton is a woman who loves a challenge, and has an infectious cackle to make anyone smile. 7 years ago, when her daughter was only 8 months old, Fran became a one-armed mum after a nasty motorbike accident. In this podcast with Emily Yates of Enhance The UK, Fran shares her hints, tips and hacks on disabled parenting and tells a good few stories, too!

‘It’s a different journey from everyone else but it’s YOUR journey. Never give up. You have to believe in yourself and make it happen.’

Fran explains how she coped adapting to becoming disabled as a new mum. Sharing tricks for fastening nappies and steering prams when you’ve only got one arm, to dealing with other peoples questions.

Disabled Parenting - Fran with her daughter Lily

Disabled parenting is a taboo subject. With a society that still sees disability as less than desirable, many of us are viewed as incapable of having and looking after children. Fran explains her capabilities as a disabled mum, and her hilarious anecdotes prove that anything is possible – finding a solution just might be a little tougher, or take a little longer.

‘One time in the play park, a dad was staring. He nudged the mum and she stared too, then their child joined it. I’d taught my daughter that wasn’t the right way to behave so when she saw them she shouted “It’s rude to stare you know!” I’m very proud of her.’

‘Don’t always pretend you’re okay. I’m really rubbish at asking for help and get myself stressed out. Remember that it’s okay to not be okay.’

Huge thanks to Fran for joining us in this podcast. Keep up to date with all our interviews, articles and more by joining us on twitter @ETUKUndressing and Instagram @UndressingDisability.

 

Julia Bahner wears a red suit jacket and a black top. She has short dark hair, red lipstick and glasses.

Interview: Julia Bahner

By Disability, Sex & disability, Undressing Disability

It’s been really exciting to see the distinctions between the different countries, both in terms of policies but also disability rights movements.
I would say that the UK has the most diverse array of disability and sexuality-focused organisations, and especially with regards to those that are led by disabled people.
Special ’sex care’ services as well as sex

Read More
A drawing of a pair of ladies pants against a yellow background

Accessing A Smear Test As a Disabled Woman

By Disability, Sex & disability, Undressing Disability

There’s no doubt you’ve heard all the statements out there about smear tests, encouraging those of us who are busy, scared or just downright lazy to crack on and book an appointment. ‘It literally takes two minutes, it doesn’t hurt, and it’s FAR more important than it is embarrassing’. All absolutely true, for the most part, but is it the same experience for a disabled woman?

Read More

Lovers In A Care Home (by Anne Taylor)

By Lifestyle, Undressing Disability One Comment

Whilst living at Arnold House, Leonard Cheshire Home, I became engaged to another Service User called Robert.

Obviously we were both disabled using wheelchairs but we wanted to be like other couples and have a good relationship involving sexual play. This proved harder than you think because we couldn’t have time together during the day as everyone was around and so couldn’t do anything. Therefore the only time we could be together was when I was in bed and and wait for Rob to come in. We couldn’t do anything until the drinks came in though, as it could have been awkward.

On one occasion we were playing and a carer didn’t knock on the door and just burst in, this made us both feel embarrassed and it just put us off doing anything. After that incident we found a way by asking the carers not to come into the room until 11pm when Rob went back to his room.

I wished we could have had more chances to play but alas it was not practical. What we did together was lovely and it made me feel like a normal couple really in love with each other and clearly sexually active.  This is not true of all homes but I feel if people are in love they should be helped to lead a proper friendship without any problems or embarrassments.

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