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Waiting game after lad s lemon-sized brain tumour s removed

Premium Content Subscriber only FOR a little boy who has already gone through so much in his young life, it s hard to find James Selwyn-Smith without a smile on his face. Like many other kids his age he s obsessed with Marvel superheroes and playing Lego. But before the age of seven he had already had five major surgeries and that was before his family knew he would be battling a medical condition they had never heard of for the rest of his life. A little over a year ago he had a tumour the size of a lemon removed from his brain.

I LOVE the skin I m in!

My differences are what make me beautiful - by Kathryn Lewsey 17 Mar 2021 Diagnosed with neurofibromatosis aged nine, Janu Dhayanathan was ashamed of her skin. Not only did the tumours that covered her body attract nasty comments from her peers, but they also caused her a lot of pain. It wasn t until Janu was in her early 20s that she decided to embrace her condition which has allowed her to feel empowered, rather than shying away from the world. Now, she s encouraging others to be kind to those with a difference.   Staring into the mirror, I couldn’t help feeling despair at the lumps that had cropped up on my face.

Brave, young Jess inspires mum to fundraise

Jess Russell (middle) with her mother, Carey and brother, Matthew. Carey’s daughter, Jess, suffers from Neurofibromatosis (NF), a genetic disorder which effects one in every 2500 Australians, and causes tumours to grow on nerves throughout the body, including the brain and spine. Carey was herself diagnosed with NF while giving birth to Jess, and not long after found out there was a 50 per cent chance the disorder would be passed on to her daughter. “I felt a deep sense of guilt when Jess started forming birthmarks all over her, because I instantly knew that she had inherited this condition,” said Carey.

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