“A child is a beam of sunlight from the Infinite and Eternal, with possibilities of virtue and vice, but as yet unstained.” – Lyman Abbott
From the moment we knew Aadriti was on her way, we felt an overwhelming mix of excitement and love. We spent nights talking about her, wondering what she’d look like, how her laughter would sound, and how life would change with her in it. Every kick of her in my womb was a reminder that our world was about to be brighter, more beautiful.
We counted down the days, longing to hold her close, to kiss her tiny hands, to watch her grow. She was already the most precious part of our lives before she even arrived.
The moment Aadriti was placed in my arms, I felt complete. She was so tiny, so perfect, and in that instant, I knew my life would never be the same. Her first cry, her soft touch, and the way she nestled into me, it was pure magic. She was our little ray of sunshine, and we couldn’t wait to see her grow, take her first steps, and call us “Mama” and “Papa.”
But fate had different plans. When she was just 1.5 months old, she was diagnosed with Spinal Muscular Atrophy (SMA). The laughter in our home was replaced with fear and uncertainty. Our precious baby, who had just begun her journey in this world, was now facing a battle no child should ever have to fight.
What’s the current condition of Aadriti?
My little Aadriti is in Peerless Hospitex Hospital, Kolkata, fighting for her life in the PICU on ventilator support.
- She has moderate to severe hypotonia, meaning her muscles are so weak that she cannot even move or do siSmple things on her own.
- Her lung function is poor, making every breath a struggle.
Now, her only hope of survival is Zolgensma.
What Is SMA?
- SMA is a genetic neuromuscular disorder that affects motor neurons.
- It has several types, with Type 1 being the most severe.
- Causes progressive muscle weakness and affects mobility and breathing.
- Symptoms usually appear between 6 to 18 months of age.
- Treatments like Zolgensma and Spinraza can improve motor function.
“I promise to fight for you until my last breath. You are my everything.”-Sima (mother)
Please save my precious angel!
Despite all the challenges, my little Aadriti has fought like a true warrior, facing every hurdle with incredible strength. She is 8 months old now.
Now, a drug called Zolgensma, worth ₹16 crore, is her only hope for a new life.
Since she was 1.5 months old, we have done everything possible, pouring in all our resources to give her the best care. But now, we are falling short.
We are desperately seeking your help to save our baby. You have the power to give Aadriti the life she deserves. Please be her hero. Donate now
Ways of becoming a hero…
DONATE: Click on the donate now button to contribute to Aadriti’s Zolgensma, which is worth crores.
SHARE: Share the story so it can reach out to more people and raise funds for my daughter’s brighter future.
আমার মূল্যবান দেবদূত রক্ষা করুন!
সমস্ত চ্যালেঞ্জ সত্ত্বেও, আমার ছোট্ট আদৃতি একজন সত্যিকারের যোদ্ধার মতো লড়াই করেছে, অবিশ্বাস্য শক্তির সাথে প্রতিটি বাধা মোকাবেলা করেছে। তার বয়স এখন ৮ মাস।
এখন, Zolgensma নামক একটি ড্রাগ, যার মূল্য 16 কোটি টাকা, এটি তার একটি নতুন জীবনের একমাত্র আশা।
যেহেতু সে 1.5 মাস বয়সী, আমরা তাকে সSর্বোত্তম যত্ন দেওয়ার জন্য আমাদের সমস্ত সংস্থান ঢেলে দিয়ে সম্ভাব্য সবকিছু করেছি। কিন্তু এখন, আমরা কম পড়ে যাচ্ছি।
আমরা আমাদের শিশুকে বাঁচাতে আপনার সাহায্য কামনা করছি। আদ্রিতিকে তার প্রাপ্য জীবন দেওয়ার ক্ষমতা আপনার আছে। তার নায়ক হতে দয়া করে. এখন দান করুন
নায়ক হওয়ার উপায়...
দান করুন: আদ্রিতির জোলগেনস্মা-এ অবদান রাখতে ডোনেট এখন বোতামে ক্লিক করুন, যার মূল্য কোটি টাকা।
শেয়ার করুন: গল্পটি শেয়ার করুন যাতে এটি আরও মানুষের কাছে পৌঁছাতে পারে এবং আমার মেয়ের উজ্জ্বল ভবিষ্যতের জন্য তহবিল সংগ্রহ করতে পারে।
The goal amount of the campaign may be higher than the attached estimates to address and aid the post-hospitalization expenses/contingencies including but not limited to prolonged medication, diagnostics, rehabilitation therapies, and follow-up doctor visits/consultations which vary from disease to disease.