Role models in the dwarfism community: Becky Curran, international motivational speaker, advocate, and consultant

Welcome back, to the second in our new series of interviews with role models in the dwarfism community. A few days ago, RGA UK VC Eugene Grant caught up with international motivational speaker, advocate, and consultant, Becky Curran.

Here’s what she had to say. You can watch her TEDx Talk here.

Please introduce yourself: who are you and where are you from?
My name is Becky Curran. I’m 33 years old. I have Achondroplasia. I currently reside in New York City. I’m originally from south of Boston, Massachusetts, attended college in Providence, Rhode Island, and spent the first six years of my career in Los Angeles, California.

And what do you do?
I’m an international motivational speaker and an advocate for diversity and inclusion on a global scale. I spend most of my days working in the diversity department at the largest entertainment union, SAG-AFTRA, where we work to ensure greater levels of inclusion in entertainment and news media for performers who have been historically excluded. This includes little people.

Do you enjoy it?
I thoroughly enjoy the work that I do. What’s really satisfying about my job at SAG-AFTRA is that I’m in front of people every single day, and am given opportunities here that I might not be given in other work places where my capabilities might be doubted.

How did you end up doing it?
I got into this work to advocate for people who are physically different. After working at a talent agency and television studio for a total of six years, I began speaking to educate as many people as possible so they don’t doubt the capabilities of people who are often left out. My work at SAG-AFTRA is an extension of my advocacy work.

If you were 21 again, would you do something different?
If I was 21 again, I would have started speaking at more schools and organizations. It took until the age of 27 for me to start taking speaking seriously. Regardless, I moved out to California at age 22. Spreading my wings that early on isn’t something I’ll ever regret.

What’s the best thing about your job?
I feel very respected at SAG-AFTRA and I love collaborating with my colleagues and our members. The schools and organizations where I speak encourage me to feel empowered.

What’s the worst job you’ve ever done?
I would say that accounting, which I did during my first internship, was something I didn’t enjoy. However, I was glad that I gave it a try and then realized that it wasn’t for me.

What are the best and worst aspects about being small?
What you see is what you get. There’s no hiding being small. However I wouldn’t want to be born any other way. All I know is how to live my life as a little person. I may want to change the way that the outside world reacts to my difference but I’m fine being little.

If you could pass on one piece of advice to your teenage self what would that be?
Be independent, stay true to yourself, and don’t get too discouraged by rejection. Everything happens for a reason and each rejection makes you stronger for the next experience.

Which living person do you most admire and why?
I admire my father. He didn’t have the easiest childhood but he went on to build the family and life that he always wanted.

How do you like to pass the time, outside of work?
I love being by the water, photography, networking, traveling, trying new restaurants, spending time with family, and writing reviews for Google.

What’s your favorite book?
My favorite book is “Daring Greatly” by Dr. Brené Brown.

What do you consider to be your greatest achievement?
In November 2013, I was asked to skip American Thanksgiving with my family and travel from Boston to Kenya, in order to help launch little people organization. Before I made my travel decision, a little person in South Africa reached out to say that she wishes that she could have the confidence that I have. I give full credit to my parents and how well they raised me. I wish that this woman had the same amount of encouragement, from an early age. In Africa, and several other countries, parents are known to hide their children if they have any sort of physical difference. I knew that receiving that message was my calling. On December 3rd, 2013, 500 people, including families who were known to hide their children in other environments, came to celebrate the launch of the Kenya Association of People with Dwarfism. From American Thanksgiving through December 6, 2013, I had the opportunity share my story all over Nairobi, in newspapers, on radio stations, television talk shows, and on stage, in order to restore faith in the community and remind them that anything is possible. Nelson Mandela died on my last night in Africa. This is pretty ironic since he reminded all of us that “it always seems impossible until it’s done.”

When your time comes, how would you like to be remembered?
Influencer of more positive portrayals in the media, which led to more acceptance for all of the amazing little people who come after me. I would like to be known for my confidence, independence, perseverance, and all that I accomplished, despite living with dwarfism in an average height world.

RGA UK and ground-breaking children’s authors urge libraries to help combat dwarfism stereotypes

School and public libraries can help combat prejudice by promoting positive portrayals of people with dwarfism, according to the new ‘Spread The Word’ campaign launched today by leading dwarfism charity, RGA UK.

The charity – which campaigns to ensure people with dwarfism have the same opportunities as everyone else – has teamed up with two ground-breaking authors to encourage school and public libraries to stock children’s books showing dwarfism in a positive and realistic light.

Supporters are encouraged to contact their public or school library to request they stock ‘Strong and Mighty Max’ by Kristina Gray and ‘We Are Giants’ by Amber Lee Dodd, as well as ‘I can’t not never be very tall’ by Susan Hatton.

Template emails and letters to send to libraries – as well as Tweets, and Facebook posts – are available from the RGA UK website. Click here.

The aim of ‘Spread The Word’ is to promote more positive and accurate depictions of people with dwarfism who are otherwise often widely mischaracterised as people from fairy tales, myths, and fantasy stories.

RGA UK believes such misrepresentations can perpetuate stereotypes, prejudice, and misconceptions among children at a young age.

Books such as these help to introduce children to dwarfism, disability, and difference in a positive and realistic light.

Both authors have some availability to visit libraries and schools and talk to children about their books.

Chair of RGA UK, Gillian Martin, said: “There is an urgent need to address depictions of dwarfism, in our media and popular culture, which too often misrepresent members of our community as people out of myths, fairy tales, and fantasy novels.

“Introducing children to dwarfism and disability – of all sorts – at a young age helps them to become familiar with and accommodate difference and diversity, which we believe should be celebrated and embraced.

“These authors have done wonders to help us achieve this and we are very proud to support their books, which should be in every library across the country.”

Commenting on the campaign, Kristina said: “I am thrilled to be part of the RGA’s campaign to combat negative stereotypes of people with dwarfism. Educating young minds with positive role models is the key to empowering the next generation to value each other’s differences as something to be celebrated and respected.

“For a child who is born with a rare condition there is no greater feeling than picking up a story book and finding out that the main character is just like you.”

Amber Lee Dodd said: “Children’s fiction can often be a powerful medium for positive social change, which is why I’m very honoured that ‘We are Giants’ has been picked by RGA to promote positive representations of dwarfism – especially as ‘We are Giants’ is about never needing to be anything other than who you are.”

‘Strong and Mighty Max’ is aimed at Early Years and Key Stage 1. Max, born with Achondroplasia (a form of dwarfism), explains that Achondroplasia is a ‘big word’ and not a special ‘superpower’; it simply means his bones grow differently. It is a wonderfully illustrated story encouraging discussion about how everyone is born different.

‘We Are Giants’, for readers aged 9+, is written from the view of a young girl who lives with her sister and her mum who has dwarfism. Her deceased father also had dwarfism. When her mum gave birth to two average-sized daughters, people were sceptical about whether she could take care of them. It has been endorsed by best-selling author, Jacqueline Wilson, and reviewed by The Guardian.

It was also nominated for a number of national awards including the 2017 Branford Boase award for most promising children’s debut novel and Longlisted for the 2017 Waterstones’ children’s fiction award.

Template emails, Tweets, and Facebook posts are available from the RGA UK website. Click here.

To find your local library visit or

Are there other books that you think positively portrays people with dwarfism? Why not add these to your list and let Team RGA know via



RGA UK is in no way commercially connected to the authors nor does the charity benefit financially from sales of these books.

We are Giants / Amber Lee DODD / Quercus Children’s Books / ISBN 9781784294212

Strong and Mighty Max / Kristina GRAY / Matador /ISBN 978178589046

I can’t not never be very tall / Susan HATTON / CreateSpace Independent Publishing Platform / ISBN 13: 9781499717747