Nicola was diagnosed with Congenital Muscular Dystrophy when she was just 18months old, she is a fun and caring girl. Currently there is no
cure or treatment for MD which is why we are raising funds to enable
research to continue and never to give up on hope.

The money raised will go into Nicola's Ninjas Family Fund which is a fund set up by us to raise as much money for research and awareness for Nicola's type of Muscular Dystrophy. 

We started the Family Fund in Sept 15 and have already raised nearly £5,000,(May 16) which is fantastic and we want to keep this going. 

Thank you all for your support, please make sure there are two very large glasses of Champagne waiting for us, we're going to need it!

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