We heard yesterday from Peter Bone, the family's MP, that Zac will receive the Monoclonal Antibody Therapy from the NHS, as part of a trial, along with other children who suffer from NeuroblastomaHe will start his treatment in mid-April, possibly in Germany, and then complete it in Nottingham under the care of the specialist who treats him at the moment.

Some of the moey raised so far will be used to pay for flights for the family to Germany, together with accommodation and living expenses whilst Zac is having treatment in Germany. Some will also be used to pay Zac's homeopathic remedies which have helped him so much. The cost of these remedies is not paid for by the NHS. We do not now have a race against time to raise £250,000 needed for treatment in New York. We will however continue to raise money in Zac's name , as the treatment he is going to receive is not a miracle cure. There is still a chance of him relapsing, and there are no relapse protocols in this country, just palliative care, so if the worst does happen he will still need to got to New York for treatment.

Once Zac is completely healthy again and there is no chance of a relapse, the money will be distributed amongst charities that help children with Neuroblastoma and other cancers, and those charities that have helped Zac in his fight. In the event that we do distribute moeny that Zac does not need we will be asking for ideas and nomination as to where it is donated.

To those of you who have donated or taken part in fund raising activities so far, we send you our most sincere thanks, and would ask that you continue your efforts.

Zac's health and wellbeing is of paramount importance to the family, and we will continue to support Bob and Sam in the decisions that they make for Zac

Thank you