Let’s help Tallulah Moon live her best life.

For his 40th, Josh has chosen to support some friends trying to find a cure for the rare genetic disease affecting their little girl, Tallulah Moon. Tallulah is a top little mate of ours, and a deadset legend, and we want to see her and other little kids like her lead the lives they deserve. We've watched her parents work so hard to pay to make this medicine and a cure is in reach thanks to amazing research. Instead of gifts, we would appreciate your support for Josh and our event by making a donation to their charity 'Genetic Cures for Kids' via our GoFundMe page to help them achieve this epic mission in time for Tallulah. Every dollar helps, we appreciate it and hope to see you at the party for a great day and night.

Do you want to join me in making a difference? I'm raising money in aid of Genetic Cures for Kids Inc. and every donation will help. Thank you in advance for your contribution to this cause that means so much to me.

More information about Genetic Cures for Kids Inc.: Genetic Cures for Kids accelerates the discovery and development of effective treatments for children living with rare genetic diseases.

Founded by Chris and Golden Whitrod, whose daughter Tallulah Moon lives with the rare neurodegenerative disease SPG56, GC4K's first mission is 'Our Moon's Mission'- to cure SPG56.

Whilst giving hope to all SPG56 families with this work, GC4K researchers are also building a replicable framework that could treat other rare diseases, of which there more than are 7000.