FOXG1 UK
Join Hands And Be A Hero
Participate in our mission to support families affected by this rare gentic disorder. Help us to find better treatments and potentially a cure for FOXG1 Syndrome
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To Know More
Meet Our Children and Adults Living With FOXG1 Syndrome
FOXG1 syndrome is a rare genetic condition that affects children from the moment they are born. The symptoms cause lifelong disabilities, placing complex and enduring challenges on those living with the condition and the families who love and care for them.
- Find us on YouTube
They Need Your Help!
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Our Mission
FOXG1 operates across the UK, working to bring hope to individuals and families affected by FOXG1 syndrome. We raise vital funds to drive research into treatments that can improve quality of life, as well as to deepen scientific understanding of this rare and complex disorder. By sharing research findings openly, we aim to benefit the wider public, raise awareness of FOXG1, and build greater understanding and compassion for the syndrome among communities, healthcare professionals, and social care services.
Volunteer Journey
Join Us in an Animal Welfare Tour
Volunteering Experience
- Jungle Safari
- Volunteering Experience
- Charity Shows
- Fund Raising
Other Experiences
- Camp Fire
- Accomodation
- Accomodation
Be a Part Of
Our Mission
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Wild Life
Forests
Food
Oceans
Clean Water
