Funds for The Neuro Foundation

Being born with neurofibromatosis (NF) have never been easy. While there's no cure for NF, there were countless follow-ups with different type specialist consultants, and lots of medical investigations like MRI, CT scan and etc. All these unique experiences helped me to truly understand the helplessness and unspoken pain of a kid with the "weird" condition. I only have a hope, and that is to help more of those with neurofibromatosis. I'm currently studying medicine, with the hope of becoming a neurosurgeon, or a researcher who will help those with similar condition as me. While I'm still on the journey to become a doctor, I've decided to do a small part for The Neuro Foundation who have been helping those with NF. I wont be able to do this alone, so I urge all of you out there to help me to make the world a better place for those with NF.

To learn more about NF, please visit The Neuro Foundation website!