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This Fundraiser will Support Multiple Patients
When strangers look at my son, they look away too quickly. Some stare. Some whisper. Some don’t know what to say. He is only 5 years old… but his face tells a story no child should ever have to carry.
My son, Daksh. It all began in November 2024 with what we thought was just dengue. A fever. Weakness. We were worried — but never prepared for what followed. Within days, his condition turned critical. Doctors said his lungs were failing. They used words I had never heard before — Severe Dengue, HLH, ARDS. I was already praying for his life when another nightmare began. A deadly fungal infection — mucormycosis — started spreading across his face.
The infection was aggressive. Merciless. It attacked his skin… his bones. Doctors rushed him for emergency surgery on 26th November 2024. I still remember sitting outside the operation theatre, numb, wondering if my little boy would come back to me alive. He did. But not the same. Parts of my baby’s face were damaged beyond recognition. The infection left him scarred and deformed. When he smiles, I can still see my Daksh… but the world sees something else first.
Sometimes he touches his face and asks me softly, “Mumma, will I look normal again?” He is too young to understand what happened. Too young to feel different. But children notice. People notice. Doctors say Daksh now needs multiple facial reconstruction surgeries to rebuild what the infection destroyed. Without them, the damage could affect his growth, speech, and confidence for life.
I am just a housewife. His father left us when Daksh was only 10 days old. Since then, we have had no support from him. My maternal family is doing everything they can, but the cost of these surgeries is far beyond our means. My son has already survived death once. Now he needs help to live with dignity.
As a mother, I am begging you — please help me rebuild my child’s face… and his future.
Your Donation Is Helping Not 1 But 3 People!
Your donation towards this fundraiser is not only helping Daksh Rai recover from Severe Dengue with HLH/Severe ARDS/Mucormycosis (Cutaneous and Osteomyelitis) but also helping two more patients in need
Karri Sridevi and her husband never imagined they would see their youngest child suffer so much. Their daughter, Sankeerthana, has Wilson’s disease, a rare disorder affecting her liver, lungs, and kidneys. Once a bright, happy child who loved studying, her condition has left her in constant pain, unable to eat on her own. She dreams of becoming a teacher, but without urgent treatment, her future is slipping away. A liver transplant is her only hope, but the cost is beyond their reach. Her parents ask for support—your generosity can give Sankeerthana a chance at a healthy, happy life.
Aradhita, 26, battles Spinal Muscular Atrophy Type II, leaving her paralyzed and dependent on her parents. Her family seeks ₹5 crores for Risdiplam treatment. Despite her artistic passion, Aradhita struggles with basic tasks. She dreams of independence but feels like a burden. Her parents, despite their love and reassurance, are helpless. Aradhita's story is a plea for help, a chance at a normal life.
Your donation towards this fundraiser will support both their treatments.
Share Campaigner
Deepmala Rai
jaipur RAJASTHAN
Beneficiary
Daksh Rai
Child
Patient Hospitalized at
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