
Tongue cancer is often thought of as a disease that affects older people with traditional risk factors. Yet an increasing number of younger adults are being diagnosed — many without any of the typical warning signs.
For those diagnosed at a younger age, the experience can be particularly isolating.
Support information is often designed for much older patients. Many people struggle to find others their own age who truly understand what they are going through. And the long-term impacts of treatment can affect careers, relationships, families and identity at a stage of life when people are still building their futures.
We bring together patients, carers, clinicians and researchers to build a global community grounded in shared experience, compassion and practical support.

Young Tongues was founded by Barbara Fountain, who was diagnosed with tongue cancer at the age of 32. Despite receiving excellent clinical care, Barbara discovered how difficult it was to find others who understood the unique challenges of experiencing tongue cancer at a younger age.
The lack of age-appropriate support and the growing number of younger patients being diagnosed made one thing clear: something needed to change.
What began as a small peer support group quickly grew into a global community connecting young tongue cancer patients across countries and continents.
Today Barbara acts as the CEO & Founder of the charity.
At the heart of Young Tongues is the belief that lived experience matters.
The wisdom shared by people who have been through diagnosis, treatment and recovery provides insight and reassurance that cannot always be found in clinical information alone.
By bringing together patients, carers, clinicians and researchers, Young Tongues creates a space where knowledge, understanding and compassion can flow in both directions.
This collaborative approach helps ensure that patient voices are heard not only within the community, but also in research, clinical practice and policy discussions.

Young Tongues is led by a dedicated group of individuals who bring together lived experience, professional expertise and a shared commitment to improving outcomes for younger tongue cancer patients.
Our work is guided by our Board of Trustees, who provide strategic oversight and ensure that everything we do remains focused on the needs of the community.
The board includes:
Laura Marston – Chair
Hannah Thorpe – Treasurer
Kate Hall – Trustee
Jake Ahmed – Trustee
Barbara Fountain - CEO & Founder, Trustee
Our mission is to provide global support, raise awareness and advocate for improved outcomes for adults aged 18 and over who were diagnosed with tongue cancer before their 65th birthday, alongside their caregivers.
Through our community, education, research collaboration and advocacy, we work to:
Diagnose sooner by raising awareness of tongue cancer in younger people
Support smarter by providing age-appropriate support and practical resources
Change the system by advocating for improved care, policy and research priorities
Lead with lived experience by ensuring patient voices help shape research, healthcare and support services
Together, these efforts help ensure that younger people affected by tongue cancer are seen earlier, supported better, and represented where decisions about their care are made.
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