About

Same but Different is a community interest company that uses the arts to raise awareness of disability and counteract prejudice.  We encourage people to look beyond first impressions and provides signposting to support organisations.

Why establish Same but Different?

Same but Different was established by photographer and marketing consultant Ceridwen Hughes (Ceridwen Barkley Photography).   This project is personal to Ceridwen as her son, Isaac, has a rare syndrome called Moebius.  From the moment Isaac was born she recognised that people made assumptions about him because of the way he looked and behaved.  Having met many parents over the years who felt the same frustrations, she decided to use her skills to raise awareness of the people behind the conditions and counteract prejudice.

The Rare Project

1 in 17 people, or 7% of the population, will be affected by a rare disease at some point in their lives.  This equates to approximately 3.5 million people in the UK and 30 million people across Europe.  There are between 6,000 and 8,000 known rare diseases which means collectively they affect a considerable number of people.  (Source: Rare Disease UK). 

As awareness around a condition grows so too does acceptance.  The aim of this project is to shine a light on some of these conditions and also highlight that just because a person has a disability it should notbe all that people see.  We want to introduce the person behind the condition.

In this project, we introduce children who have rare conditions, through a series of high profile exhibitions, an online gallery, social media and press articles.  It will allow people to learn more about the impact of rare conditions on children.

If you would like to take part please click here to see how.

To find out about some of our Partners in this project click here.

 

 

To keep informed of what is happening with Same but Different please complete the following form.  We do not supply your details to any third party organisation.

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Ceridwen Hughes

Ceridwen Hughes

Adelina's daughter

Adelina's daughter

“I needed time to realise that having a daughter with a disability is a blessing. This project really helped me to show other families in the same situation that they are not alone. It also allows us to show people who don’t know much about disability that being kind is all that children need from us.” Adelina, daughter has Patau Syndrome