Jelome's Journey from PNG to Australia for his surgical treatment
Feel Good Friday!
Starting off the year with extraordinary news:
I am overjoyed to welcome little Jelome, and his mum Lily, to Australia as he begins his surgical journey!
Many of you followed Jelome’s story through our Christmas appeal – born with multiple congenital anomalies including a bilateral cleft palate, severe spina and fused fingers. If you’d like to know more about his medical needs, you can find further details here.
His safe arrival is all thanks to you and your generosity, which has meant the world to Lily!
Despite being far from home, Jelome has adapted incredibly well. He has already met with several specialists who assessed his needs in person and planned the best way forward. I feel incredibly lucky to have a fantastic team of specialists who want to, and can, improve Jelome’s chances of a happy and healthy future!
Leading his care is Dr Mark Moore, world-renowned craniofacial and plastic surgeon who will oversee Jelome’s reconstructive surgery for his cleft palate.
Jelome may have made it to Australia but his complex surgical journey is only just beginning. Jelome's treatment includes multiple procedures and far from finished. That's why you might still see his story being shared - he needs ongoing support to complete his surgical care.
I hope you join me in getting to know Jelome better over the coming weeks, and in sending him your best wishes as he begins treatment and recovery.
I am full of hope for the future. Your care and compassion continue to shine a guiding light for the children who are, and will, receive life-changing care this year.
Jessica Redwood early 2026 reflection
Thank you for choosing humanity in unsteady times.
With my sincerest thanks,