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I am raising funds for my daughter, who is just 4 months old. Our family is going through an incredibly difficult time as she fights a rare and life-threatening condition at such a tender age. she is the light of our lives. Seeing her struggle like this has been heartbreaking for our entire family.
She has been diagnosed with Spinal Muscular Atrophy Type 1 (SMA Type 1), a severe genetic disorder that affects muscle strength and movement, and requires urgent and specialized treatment to survive.
She is currently receiving medical care at the All India Institute of Medical Sciences, though she has not yet been admitted, and is under medical supervision.
This situation has been emotionally devastating and financially overwhelming for us. Until now, we have only been able to spend around ₹12,000 on her initial medical needs, which we arranged through our savings. However, the treatment required for SMA Type 1 is extremely expensive and beyond our means.
In the next few days, we urgently need ₹15,00,00,000 (15 crore) to proceed with the life-saving treatment that can give our little daughter a chance to live.
We humbly request everyone to please come forward and support our baby girl during this critical time. Any contribution, no matter how small, will make a meaningful difference and bring us closer to saving her life. Please donate and share this fundraiser with your friends and family so that more people can come together to help her get the treatment she desperately needs.
Your kindness, prayers, and support mean everything to us during this painful time.
मैं डॉ. रोहित दुबेपुरिया हूँ। मेरी पत्नी प्राकृति सिसोदिया हमारे 4 महीने की बेटी के इलाज के लिए धन जुटा रही हैं, जो एक दुर्लभ और गंभीर बीमारी स्पाइनल मस्कुलर एट्रोफी (SMA टाइप 1) से जूझ रही है। वह हमारे जीवन की रोशनी है, और इतनी छोटी उम्र में उसे इस तरह संघर्ष करते देखना हमारे पूरे परिवार के लिए बेहद दर्दनाक है।
वह वर्तमान में इंदौर में डॉक्टरों की देखरेख में है, और डॉक्टरों ने तुरंत जीवनरक्षक उपचार की सलाह दी है। लेकिन यह इलाज बहुत महंगा है, और हम इसे अपने दम पर वहन करने में असमर्थ हैं।
हमें उसके इलाज के लिए तुरंत ₹15 करोड़ की आवश्यकता है।
हम इस कठिन समय में आपसे विनम्र अनुरोध करते हैं कि कृपया हमारी मदद करें।
She has been diagnosed with Spinal Muscular Atrophy Type 1 (SMA Type 1), a severe genetic disorder that affects muscle strength and movement, and requires urgent and specialized treatment to survive.
She is currently receiving medical care at the All India Institute of Medical Sciences, though she has not yet been admitted, and is under medical supervision.
This situation has been emotionally devastating and financially overwhelming for us. Until now, we have only been able to spend around ₹12,000 on her initial medical needs, which we arranged through our savings. However, the treatment required for SMA Type 1 is extremely expensive and beyond our means.
In the next few days, we urgently need ₹15,00,00,000 (15 crore) to proceed with the life-saving treatment that can give our little daughter a chance to live.
We humbly request everyone to please come forward and support our baby girl during this critical time. Any contribution, no matter how small, will make a meaningful difference and bring us closer to saving her life. Please donate and share this fundraiser with your friends and family so that more people can come together to help her get the treatment she desperately needs.
Your kindness, prayers, and support mean everything to us during this painful time.
मैं डॉ. रोहित दुबेपुरिया हूँ। मेरी पत्नी प्राकृति सिसोदिया हमारे 4 महीने की बेटी के इलाज के लिए धन जुटा रही हैं, जो एक दुर्लभ और गंभीर बीमारी स्पाइनल मस्कुलर एट्रोफी (SMA टाइप 1) से जूझ रही है। वह हमारे जीवन की रोशनी है, और इतनी छोटी उम्र में उसे इस तरह संघर्ष करते देखना हमारे पूरे परिवार के लिए बेहद दर्दनाक है।
वह वर्तमान में इंदौर में डॉक्टरों की देखरेख में है, और डॉक्टरों ने तुरंत जीवनरक्षक उपचार की सलाह दी है। लेकिन यह इलाज बहुत महंगा है, और हम इसे अपने दम पर वहन करने में असमर्थ हैं।
हमें उसके इलाज के लिए तुरंत ₹15 करोड़ की आवश्यकता है।
हम इस कठिन समय में आपसे विनम्र अनुरोध करते हैं कि कृपया हमारी मदद करें।
