Hi, I'm Yroh. 💛

I am a proud little warrior living with DIPG (Diffuse Intrinsic Pontine Glioma), G6PD Deficiency, Rh-Negative Blood, and the challenges of being born premature.

My Doctors Said i have 5-15 months left to live but i am brave and strong, im going to fight with all my might

Every day brings obstacles, hospital visits, treatments, and uncertainty, but it also brings courage, hope, and strength. My journey may be difficult, but I continue to smile, fight, and inspire.

Today, I share my story not for sympathy, but for awareness. Please help spread knowledge about DIPG, support children facing medical battles, and keep all warriors like me in your prayers.

As of today , the only treatment I'm receiving is traditional Chinese medicine, weekly check-ups, my parents are also planning to give me ozone therapy, 1900 every 2 weeks to increase my strength and take ivermectamine and fenbendazole. I'll also have an MRI in July to see the progress of my tumor.

I am 7 months post diagnosis and doctors told us that after 5 month my tumor will begin to progress, thats why were going to apply all the medical trials.

Yes, everything is a trial because my cancer is incurable and inoperable, but we will do everything we can to extend my life,

Thank you for sharing this journey with me.