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Our Charity 2025

At Griffins, we believe in giving back and making a real impact. Each year, we partner with a different charity to help raise funds and awareness for their incredible work. By supporting a variety of causes, we aim to shine a light on important issues and extend help where it's needed most. Our partnership allows us to amplify their message, but the most powerful support comes from you. If you wish to join us in supporting this cause you can donate directly and be a part of something truly meaningful. Together, we can make a difference—one cause at a time.

This year we are supporting Angelman UK.

Angelman UK logo.PNG

Angelman Syndrome is a rare genetic disorder that affects the nervous system, causing developmental delays, speech impairments, and balance issues. It is caused by a mutation or deletion of the UBE3A gene on chromosome 15. People with Angelman Syndrome often exhibit a happy demeanor, frequent laughter, and an affinity for social interaction, but they also face challenges such as seizures, sleep disturbances, and difficulty with motor skills. While there is currently no cure, therapies and interventions can help improve quality of life. Raising awareness and supporting research is crucial to finding better treatments and, one day, a cure for those living with this condition.

Let's Talk...

If you would like to discuss a particular scenario with us, or would like an initial consultation, please contact us by: 

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