Support. Awareness. Inclusion.
Raising awareness and providing comprehensive support for individuals and families affected by Treacher Collins Syndrome and other craniofacial conditions, fostering understanding, inclusion, and empowerment through community engagement, education, and advocacy efforts to promote acceptance and improve lives worldwide.
The relief of people with treacher collins syndrome (tcs) and other craniofacial conditions and their families, in particular by the provision of information, advice and financial support for essential medical supplies/procedures.
Advance education and promote a wider knowledge and understanding of the problems of treacher collins syndrome (tcs) and other craniofacial conditions amongst the public.
About us
Love Me Love My Face is a charity dedicated to supporting individuals with Treacher Collins Syndrome (TCS) and other craniofacial conditions. We raise awareness, provide resources, and offer support to help those affected live fulfilling lives with confidence and dignity. Our programs include financial assistance for medical treatments, access to educational materials, and community events that foster connection and inclusion.
Get Involved: Donate, volunteer, or spread awareness to make a difference. Support us by clicking the heart icon on our website to donate via "Give as You Live," where a portion of your online shopping contributes to our cause. Together, we can create a more inclusive society and help everyone feel proud of who they are.
What Our Customers Say
"Love Me Love My Face has been a lifeline for our family. The support and resources they provide have made such a difference in our journey. We feel truly seen and supported."
— Sarah, parent of a child with TCS
"This charity gave me a place to belong. Through their events and outreach, I’ve connected with others who understand my experience, and it’s been incredibly empowering."
— Jack, individual with a craniofacial condition
"The financial assistance for my medical treatments and the kindness of this community have given me hope, confidence, and strength to face the world every day."
— Emma, beneficiary
Common FAQ's
1. What is Treacher Collins Syndrome (TCS)?
Treacher Collins Syndrome is a rare genetic condition that primarily affects the development of facial bones and tissues. It can result in challenges with breathing, hearing, eating, and speech, as well as distinct facial differences. While TCS does not affect intelligence, individuals often face social and emotional challenges.
2. How does Love Me Love My Face support individuals with craniofacial conditions?
We are committed to helping individuals and families affected by craniofacial conditions through financial assistance for medical treatments, including surgeries and therapies. We also provide access to educational resources, advocacy, and community programs that create opportunities for connection, understanding, and support.
3. How can I get involved with the charity?
There are many ways to make a difference! You can donate directly, volunteer at our events, or participate in fundraising activities like our Yorkshire Three Peaks challenge. Additionally, spreading awareness about our mission and sharing our story on social media helps amplify our impact and reach.
4. How do donations help the charity?
Every donation we receive directly supports our mission. Your contributions fund vital medical treatments, including surgeries and hearing aids, provide families with educational resources, and allow us to organise community events. These initiatives promote inclusion, understanding, and a better quality of life for those with craniofacial conditions.
6. How can my company support Love Me Love My Face?
Businesses can support our charity by partnering with us for fundraising events, offering sponsorships, or promoting our mission through corporate social responsibility initiatives. Additionally, companies can match employee donations, host awareness campaigns, or volunteer at our events. Your company’s support helps raise vital funds and creates a positive impact on the lives of those living with craniofacial conditions.