Families Against Neuroblastoma is the first port of call for anyone who has received the devastating news that their child, or loved one, has Neuroblastoma.

We are a charity solely dedicated to providing support, information and assistance in all aspects of dealing with Neuroblastoma, and who seek to fund specific research into cutting edge treatments of Neuroblastoma.

We can help you with all the questions that arise from initial diagnosis, and give you further advice on treatments not currently available on the NHS or in the UK. should you wish to opt for one of these treatments, we can assist you with launching and running an appeal for your child, and manage your funds and medical expenses for you.

regardless of the treatment you choose, we believe life is for living, and we provide family fun days out, usually once a month, and try to put a smile on every one's face whenever we can :)
We can also arrange wishes for children under 3 years of age, and wishes for siblings of all ages. We can assist with wish granting foundations for every child that qualifies. FAN firmly believes in treating all children equally, and we understand the devastation siblings can experience at this time. Our FAN club is growing all the time, and we have children of all ages who are going through this together.

FAN is run by families of NB, for families of NB. we very much see ourselves as an extended family, and always welcome new members. we also welcome those of you who have sadly lost a child to Neuroblastoma, as many of us here have, and we encourage you and your children to come along on our family days and meet others who have also lost the battle. We know this can be upsetting, but it really can help too.

Although we are new as a charity, we have been around as a group for over a year. some of our members have been involved with Neuroblastoma for many years. We are different because we all know what its like to go through this, and how much better it can be to not go through it alone.

Together we are stronger.