Abandoned at birth due to a deformity, he became a model and actor

Jono Lancaster (36) is a model and actor United Kingdom who has been recognized for his work as an activist for the rights of people with facial abnormalities. Jono suffers from Treacher Collins Syndrome, a genetic disease that affects the cheekbones, jawline and ears. He has used his he platform to educate and raise awareness about the acceptance of diversity and the elimination of discrimination.

Jono started the charity Love me, love my face , which seeks to provide emotional support and practical advice to people with facial abnormalities. In addition, she has lectured at schools and companies on the topic of diversity acceptance and inclusion.

Jono continues to work as a model and actor as well as star in documentary seriesl “Jono Lancaster: Limitless” (2021) and work on expanding your organization. Through his activism and his work, the man has shown that no matter what he looks like, everyone is valuable and important and has inspired others to move forward in life with confidence and determination.

A life of struggle and acceptance

Jono Lancaster was born on September 30, 1985 in North Yorkshire, a rural area of England. Since birth, Jono suffered from Treacher Collins syndrome, a congenital disorder that affects the development of the jaw, cheekbones and ears, which gave him a different physical appearance from others, with a very small jaw and ears of very little cartilage

Since childhood, Jono has faced various difficulties due to his condition, especially with regards to his appearance and hearing. Jono he was bullied at school and suffered greatly from rejection and discrimination from other children.

In his adolescence, the young man became more aware of his condition and decided to take control of his own life. He began to participate in sports and artistic activities, which allowed him to discover his talent for acting and singing.

Despite the barriers placed before him, Jono set out to become a role model and spokesperson for people with STC and other disabilities. He started working with charities and support groups and also became an international activist. Despite the obstacles created by his physical appearance, Jono remained positive, worked hard and made a career in the modeling industry, appearing in advertising campaigns and magazines such as Men’s Health and GQ.

Years of struggles and sacrifices

After his story made headlines in the British media, Lancaster set up the charity in 2013 Love me, love my face, which focuses on educating and raising awareness about people with facial abnormalities and fighting the discrimination they experience. He has also appeared in several television shows, including the documentary series ‘Love Me, Love My Face’.

Jono has been invited to speak in schools and companies on the topic of welcoming diversity and inclusion. He has also traveled to other countries to talk about his experience and raise awareness of facial abnormalities.

In an interview with Huffington PostJono spoke about her focus on self-acceptance and fighting discrimination: “No matter what you look like, no matter what you look like, no matter what you lack, you are valuable. You are important. You are needed.”

Jono has been recognized for his work and activism. In 2015 he was awarded the ‘Positively Yorkshire’ award by BBC, in recognition of their excellence in promoting diversity and inclusion. He has also been appointed as an ambassador for Changing Faces, a UK charity that works with people with facial differences.

recognition has come

Today, Jono Lancaster continues to work as a model and actor and remains an active advocate for the rights of people with facial differences through his charity. Lately, Jono has been working on a documentary series called “Jono Lancaster: Without Limits” which chronicles his experience of traveling the world and meeting people with similar facial differences to his.

In February 2021, Jono shared that he got engaged to his girlfriend, Laura Richardson, in an Instagram post. He has also been an advocate for the importance of mental health, especially during the COVID-19 pandemic, and has shared his experience with anxiety and depression on social media and in interviews.

As for its organization, Love Me Love My Face has continued to provide emotional support and practical resources to individuals and families affected by facial differences. In March 2021, they announced they had received a grant from the UK National Lottery to expand their reach and provide further support to the community.