In September 2005 I became a mummy for the first time and everything changed.  

At 11 weeks we were told that our baby had a rare disorder and that she may not survive. Each appointment seemed to discover something else, another hurdle for our little girl.  At 20 weeks into my pregnancy Sofia was born and my heart just broke. She was so small and I never wanted to let her go. The months that followed were so hard but we decided that her little life had to be a bright light for others, that she would make a difference to the world and for other children and their families. 

We have been fundraising every year since then for Jeans for Genes in Sofia’s name and are proud that she has made a difference to so many lives. I’d be so grateful if you can spare a few minutes to read about the incredible work they do, and if you can spare a little change that that would be amazing..........

Jeans for Genes Day is the annual fundraising campaign for Genetic Disorders UK, the national charity that supports children affected by a genetic disorder. The monies raised on Jeans for Genes Day provide grants for day-to-day support, equipment, respite and events which bring together affected children and their families.Who we helpThere are between 4,000 and 6,000 diagnosed genetic disorders. It is estimated that one in 25 children is affected by a genetic disorder and therefore 30,000 babies and children are newly diagnosed in the UK each year. Some genetic disorders are apparent at birth while others are diagnosed at different stages throughout childhood, and sometimes into adulthood. Find out more: https://www.jeansforgenesday.org/our-workWhat we doWe help disorder-specific charities and patient groups to deliver inspiring projects and support services for children affected by a genetic disorder in the UK. Find out more: https://www.jeansforgenesday.org/who-we-are