Story
Anyone who has a child diagnosed with Ataxia Telangiectasia (A-T) realises immediately and agonisingly that their lives will be changed forever and that the future holds a number of very difficult challenges for their child both physically and emotionally.
Founded in January 2012 by parents of a child diagnosed with A-T, Action for A-T understand what that feeling is like and is committed to making a difference to those affected by funding high quality medical research.
In the UK, research funding for A-T is extremely limited so Action for A-T was established to increase investment in A-T research and raise awareness of the condition.
We will be cycling 240 miles from Blackbushe, England to Arras, France over three days, in order to raise as much money as possible for Action for A-T. Please help me reach my fundraising goal!
