Mollie was born with a rare genetic disease called Ataxia Telangiectasia or A-T for short. To most people this won’t mean anything as they are likely to have never heard of A-T, but to us it has shattered our world.

A-T is a disease that affects children, it initally causes loss of balance and coordination leading to walking with a wobble or sway (ataxia). A delay in fine and gross motor skills means kids with A-T learn every day skills more slowly with difficully then to gradually loose these skills and becoming fully dependant on a wheelchair by the age of 10 along with suffering tremors and speech and swallowing difficulties. A-T also causes major problems to the respiratory system and causes immune deficiency along with a hugely increased risk of childhood cancers.

No words can describe the suffocating feeling of having your child diagnosed with an incurable disease like A-T.

Our beautiful, happy little girl is so loved and deserves the best chance in life - right now there are no treatments or a cure available for this devastating disease and we know the best way to help Mollie will be to have regular physiotherapy, hydrotherapy and specialist therapies and equipment.

Any donation made will be making a big diffence to helping Mollie live life to the full.

Thank you x