Tristan Thornton
Tristan Thornton
Tristan was born in Christchurch in August 2007 with a rare genetic Primary Immune Deficiency Disorder ( Di George Syndrome); Tristan effectively had no natural immunity against infections.At 7 weeks of age was still living in isolation at Christchurch Hospital - unable to venture out for fear of infection.
Doctors recommended a rare Thymus transplant which could only take place in the United States. The KIDS Foundation supported Tristan and his family through this journey, offering hands on support and help in fundraising.Both parents wanted to accompany Tristan to the USA and the Foundation was able to help make this happen.
Tristan underwent his transplant in October 2007 and returned to New Zealand early in 2008. The operation was successful and his parents were thrilled to be able to take him home for the first time.
Now a happy 2 year old - Tristan is doing well. However he still needs regular immunoglobulin treatment which he has at home weekly, and has other related medical conditions that are being treated. His family guard his health carefully but he is enjoying a good quality of life. Tristan has recently been joined by a new baby brother who will be a welcome playmate for him.
