David and Emma Mills, originally from Swords but now living in Donabate have issued an urgent appeal for support for their baby girl Zoe who is being treated for stage 4 high-risk neuroblastoma, an extremely aggressive childhood cancer. All funds raised will support Zoe’s participation in a US-based clinical trial.
A happy baby who was meeting all her milestones, little Zoe suddenly became unwell in August 2023. Scans showed that a tumour attached to her kidney, and taking up 50% of her abdomen, had spread throughout her tiny body and fully into her bone marrow. The severity of her prognosis meant that Zoe had to start an intense 18-month treatment plan immediately.

Since then, Zoe has bravely battled through chemotherapy and intricate abdominal surgery to remove as much of the main tumour as possible. She has also undergone additional high dose chemo and a stem cell transplant requiring 6 weeks of isolation in a dedicated transplant unit; 14 sessions of radiotherapy, each one carried out under general anaesthetic; and countless blood transfusions, injections and medical procedures.

Zoe is currently undergoing the immunotherapy phase of her treatment, 5 cycles over 6 months, with the first 2 cycles requiring a morphine pump to manage her pain. Immunotherapy will hopefully be the final stage of Zoe’s frontline treatment, and it’s hoped that her post treatment PET scan will show “No evidence of disease”.

David and Emma are committed to doing all they can to give Zoe the best chance of a long and healthy life. They are aware that the outlook for neuroblastoma can be bleak, with a very high relapse rate, and limited treatment options if relapse occurs. This makes the longer-term survival statistics unthinkable.
On the anniversary of Zoe’s devastating diagnosis, David and Emma, together with family and friends, have launched a fundraising campaign called “Hope for Zoe” to try and raise as much money as possible to access a clinical trial in the USA.

Today, Zoe is doing her best to stand up and take a few steps, say a few words, and even ‘sing’ along to her favourite movie, Frozen! She is getting used to her hearing aids, which were necessary after the hearing loss caused by chemo and communicating better every day. Her feeding tube is still required for her nutrition and daily medication. She is full of personality and fun, and extremely determined! It is the hope of all who love her that she can gain access to a clinical trial and thrive, just like every other child.
For further information please contact Philip Farrell (087-7562450) or (hopeforzoe2024@gmail.com)