Everyday in the UK a child is born with mitochondrial disease or "Mito".It can be debilitating and cuts too many lives too short.Currently there is very limited treatment and no cure.The Lily Foundation, a charity dedicated to funding research and supporting those affected want to change this. I've been inspired to support them because of Samantha, who despite being diagnosed with the condition wants to help to change the future for others. So please donate if you can and visit www.mitoandme.com, and www.thelilyfoundation.org.uk for more information.