Jack, now six years old, has been battling this disease for nearly two years. This has meant his parents, brother and sister moving to New York and living in one room in a hostel whilst he was treated at the Sloane Kettering Memorial Hospital. After a short spell back in England, Jack and his family have relocated to Vermont where Jack is undergoing further treatment. Read the updates on www.jackbrownappeal.org
Seven year old Hannah is still attending her school and going to her brownie pack despite the frequent pain that she encounters from chemotherapy and a high level of antibiotics. So far her treatment has been in England but the possibility of a future trip to New York cannot be ruled out. Follow her progress on www.hannahedwardsappeal.org
Two great pieces of news for six-year old Jacob right now – his latest bone marrow tests are free of cancer and he is going to be a walk on mascot for his favourite team Manchester United in the Champions League match against Olympique Lyonnais on 4th March. Latest instalments from Jacob’s diary on www.jacobmarslandappeal.org
Grace was diagnosed with stage 4 neuroblastoma in October 2007 and her parents opted for her to be taken to the Memorial Sloan Kettering Hospital (MSKCC) in New York for surgery & Monoclonal Antibody Treatment- with an 80% survival possibility. Grace and her family moved in the first week in January and she underwent her first surgery within a fortnight. For all developments go to www.graceogorman.co.uk
Phoebe Macaskill, the newest member of the 2Simple 'family' is a two year old little girl from Inverness recently taken into Yorkhill hospital in Glasgow . On 16th April 2008 she was diagnosed with Neuroblastoma, stage 4, a rare and aggressive childhood cancer. Phoebe has now started chemotherapy after having to endure many complicated diagnostic procedures in the past few weeks. You can follow her story on her site.
Very sadly George passed away at the age of nine in January 2008 after a brave and courageous struggle, supported by his parents Martin and Helena and a large number of family and friends. His parents have asked that the website be kept open and that donations towards the general 2Simple Trust campaign for children with neuroblastoma in his memory would be greatly appreciated. Read his story on www.georgeyeomansappeal.org