Show your love and support to the Pope Family and let them know they are not travelling this journey alone.
Auckland
Logan was born with Neurofibromatosis (NF1), a rare genetic condition that caused tumours to grow in his optic nerves and brainstem; like 50% of people with NF1, Logan also has learning challenges and has been diagnosed with ADHD.
To treat the tumours, Logan has spent time in and out of the hospital over the past two years, receiving intravenous and oral chemotherapy, and more recently started a six-week course of radiotherapy. Because of the demands of his treatment and the side effects they cause, Logan has missed out on many childhood experiences that healthy children take for granted.
Logan is supported by his amazing family, who are by his side every step of the way. Hayley and Rodney, Logan's parents; his big sisters Micaela and Teagan and his special fur brother, Jasper the Therapy Dog.
Once committed volunteers in their community, Hayley and Rodney now focus their energy on their family as they juggle work and school commitments alongside Logan’s treatments. Hayley is devoted to Logan's full-time care and lives at Ronald McDonald House in Auckland. Rodney commutes between Auckland and Waiheke whilst caring for the girls, who travel back and forth to spend time with their brother and attend school.
We know people care about the Pope family and want to help them during this unimaginable time but are unsure what to do. Here is your chance to show your love and support and to let this deserving family know they are not travelling this journey alone.
Logan is my nephew
Any funds raised will help the Pope Family spend quality time together away from hospital appointments and medical treatments to relax, reconnect, and have fun so they can recapture some of the precious moments they have lost due to Logan’s illness.
Funds will be paid to Logan's mum Hayley
Home again. 16 September 2023
Logan finished the six weeks of radiotherapy treatment two weeks ago. Being home has reminded us just how important the little things are, like having breakfast first thing in the morning and not waiting until after treatment, waking up in our own beds, and being home together at the end of each day.
Unfortunately, we are facing another unexpected challenge with Logan's treatment. We noticed his walking and balance deteriorating recently, so he is retaking steroid medication to reduce the inflammation in his brain. We hope his condition will start to improve in the coming days.
However, thanks to your support, we have something special to look forward to. We are going on a family holiday to the Gold Coast to visit Seaworld, swim with dolphins and ride the waterslides at Wet and Wild in the October school holidays – something we could never have considered had it not been for the kindness shown to us on this this give a little page.
Thanks again for supporting our family. We will be sure to send another update in the coming weeks.
Your message will be displayed on the page and emailed to the donor.
Your new message will also be emailed to the donor.
Saving a blank entry will delete the current comment.