This issue of Touching Lives features two families whose lives have been affected by an inherited disease that can damage children's lungs and airways. Little Malachi was given an early diagnosis but not all children are as fortunate, so Action is funding research to ultimately help speed up diagnosis.
You can also read about how a gift in the will of Gordon Walkinshaw helped the family of two-year-old Jack, who was born with a genetic eye condition called primary aphakia.
Elsewhere in the magazine there are updates on our Touching Tiny Lives appeal, our research into a vaccine for MenB and projects on sickle cell disease, obesity, movement difficulties and preventing premature birth.

With your help we're funding research into a debilitating genetic disease that affects children’s lungs and airways, making them more susceptible to infection. This work should help provide early diagnosis, something two mothers welcome.
One man’s gift is funding important research on the genetic cause of childhood blindness. This has given one family some much-needed answers about their young son’s condition.
Our patron, HRH The Prince Philip Duke of Edinburgh, hosted a drinks reception for 150 specially invited guests at the Palace of Holyroodhouse in Edinburgh in August. Attendees included some of the best medical researchers working in Scotland.
