“Every time I hear the sound of her breathing machine, I remind myself my baby is still fighting… and I cannot give up on her.” - Rohini Chauhan, mother.

Every morning, I wake up praying that my daughter is still breathing. My baby, Garvika, is only 4 months old. At this age, babies should be smiling, kicking their tiny legs, reaching for their parents, and filling the home with laughter…

But my daughter cannot even lift her little hands. She cannot move her legs. She cannot hold her neck. She cannot breathe on her own.

Instead of hearing her soft coos, I hear the sound of machines, the BiPAP that helps her breathe… the feeding tube that keeps her alive.

When Garvika was just 45 days old, our world changed forever. Doctors told us she has Spinal Muscular Atrophy Type 1, a rare genetic disorder that slowly takes away a child’s ability to move, swallow, and even breathe.

“As a mother, nothing prepares you for hearing that your baby may not live to see her second birthday.”- Rohini Chauhan, mother.

Every single day, I watch SMA steal a little more of my daughter’s strength. Her sister watches her with tears in her eyes.

Doctors have told us there is hope… One life-saving dose of ₹9.5 crore Zolgensma could give my baby a chance to live and a chance to call me “Mama” someday.

My husband works as a government employee, and despite doing everything we can, this treatment is beyond what our family can afford.

“As a father, nothing hurts more than watching your little girl struggle for every breath while knowing there is a treatment that could save her.” - Raj Kumar, father.

We ask as a family hoping to save our baby. Please help us give little Garvika the timely treatment she deserves.

Help Garvika live a healthy childhood!

How can you help her?

Donate to her treatment.

By donating, you help ensure that she receives the treatment that saves her life.

Share her story with your family and friends.

By sharing her story with your loved ones and friends, you will help to amplify her voice to those who care and are willing to donate.

*****

महज चार महीने की उम्र में, गारविका स्पाइनल मस्कुलर एट्रोफी नामक एक दुर्लभ बीमारी से जूझ रही है, जो दिन-प्रतिदिन उसकी मांसपेशियों को कमजोर करती जा रही है।

वह अपने छोटे-छोटे हाथों, पैरों को उठा नहीं सकती, यहाँ तक कि अपनी गर्दन को भी नहीं संभाल सकती, और अब सांस लेने के लिए BiPAP सपोर्ट पर निर्भर है।

ज़ोलजेन्स्मा की एक जीवनरक्षक खुराक गारविका को सांस लेने, चलने-फिरने और जीने का मौका दे सकती है।

आपका दान एक बड़ा बदलाव ला सकता है!

आप उसकी मदद कैसे कर सकते हैं?

उसके इलाज के लिए दान करें।

दान करके, आप यह सुनिश्चित करने में मदद करते हैं कि उसे वह इलाज मिले जो उसकी जान बचाएगा।

उसकी कहानी अपने परिवार और दोस्तों के साथ साझा करें।

अपने प्रियजनों और दोस्तों के साथ उसकी कहानी साझा करके, आप उसकी आवाज़ को उन लोगों तक पहुँचाने में मदद करेंगे जो उसकी परवाह करते हैं और दान करने को तैयार हैं।