<p><strong>TOFS </strong>: This charity provides support, help and information to families of children born with the <strong>TOF/OA </strong>condition. They coordinate research into the condition and provide booklets, leaflets and conferences to educate and raise awareness of this rare condition.</p> <p>This proved to be an invaluable source of help and information to us when we first found out that Oliver had been born with the condition. It affects around 1 in 3500 children born with varying degrees of severity. Despite much research the exact cause of this congenital anomaly is unknown. TOFS help families children with the condition through networking, family days, conferences and publications to increase awareness of this not so uncommon condition.</p> <p>So please dig deep and donate now and <span style="text-decoration: underline;">don't forget to tick the Gift Aid box</span> to maximise the donation.</p> <p>Many thanks for your support and helping us to make the most of our little boy's short but happy life.</p> <p>Lee and Gail</p>