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On Sunday 15th September, Jack’s mum - Jenna, has roped in several family members - Anne, Jill, Jonathan, & Geraldine to take part in the Edinburgh Kiltwalk to raise vital funds and awareness for Angelman UK.

Jack was diagnosed with Angelman Syndrome in December 2020 when our lives changed forever. Angelman Syndrome is a rare genetic condition which affects all aspects of Jack’s life and means he will need lifelong support.

We would like to give a little back to the charity that helped Jack’s family through diagnosis and continue to help families affected by Angelman Syndrome. As well as offering extremely helpful advice, they are able to help raise funds for specialist equipment for children like Jack, access to further support and practical help when required. Any donations to this wonderful charity would be gratefully appreciated.

Wish us luck!