Editor's notes...

In the previous issue we looked at how a diagnosis of childhood cancer affects not just the child, but his or her whole family. 

Diagnosis is the theme of this issue, and we again feature articles from families highlighting the impact of diagnosis, but also articles from healthcare professionals. It is clear from the latter that there are significant issues related to the rarity of childhood cancer and the complexity of diagnosis, which can sometimes lead to delays in a definitive diagnosis. Awaiting a firm diagnosis, when it is possible that the news may be serious, is an incredibly anxious time. For some, knowing the diagnosis and what the treatment plan will be, can be a comfort. For all families, however, after a diagnosis of childhood cancer, life will never be the same again – a view summed up by Corisande Albert on page 1: “last year was separated into BC (before cancer) and AD (after diagnosis)”. 

You will be aware that we now have a different sponsor for each issue of Contact. We are very grateful to Kamran’s Ward Charitable Fund, Oxford Children’s Hospital, for their generous sponsorship of the current issue.