Pt. Baby of Nisha
₹ 1,000
tax benefit: 50%
|
BABY OF NISHA |
From the moment he was born in Lucknow, Baby of Nisha brought immeasurable joy to his parents. As their first and only child, he quickly became the center of their world — a bright, healthy newborn who filled their hearts with hope. For a while, everything seemed perfect.
However, just weeks after his birth, subtle but alarming signs began to emerge. His lips and nails started turning bluish — a possible sign of oxygen deficiency. His nails also began appearing broader and clubbed, and he developed troubling bowel issues. Deeply concerned, his parents rushed him to the hospital where he was born. After an initial assessment, the doctors suspected a congenital heart defect (CHD) and referred them for further testing.
Their fears were soon realized. The echocardiogram pointed toward a serious heart condition. The news was devastating, and tragically, Nisha’s husband could not bear the emotional shock. He passed away shortly after the diagnosis, leaving Nisha alone to care for their infant son. The baby was just 1.5 months old when he lost his father.
In the months that followed, Nisha’s world collapsed around her. She returned to her parental home, now the sole caregiver to her child while also depending on her elderly parents and supporting her younger, school-going sister. With no financial stability and her own grief weighing heavily on her, Nisha struggled to access the medical care her baby urgently needed. For over a year, his condition continued to deteriorate.
Eventually, Nisha brought him to KGMU Hospital in Lucknow, desperately seeking help. But despite her efforts, she found no solution. Just when all hope seemed lost, she met a compassionate hospital staff member named Mr. Gurmeet.
He guided her to Child Heart Foundation — and that meeting changed everything.
At the Child Heart Foundation in Delhi, under the expert care of Dr. Kohli, the baby underwent a thorough re-evaluation.
A fresh echocardiogram was performed, and the final diagnosis was confirmed:
Double Inlet Left Ventricle (DILV) with Large Inlet Ventricular Septal Defect (VSD) and Peri membranous Extension — a complex congenital heart defect where both atria drain into the same ventricle, impairing the heart’s ability to deliver oxygen-rich blood to the body.
Dr. Kohli confirmed that immediate surgical intervention is essential. The child now requires a two-stage treatment:
- Cardiac Catheterization (CATH)
- Glenn Shunt Surgery — a palliative procedure that improves blood flow to the lungs.
The cost of this life-saving treatment is approximately ₹4 lakhs — an amount far beyond what Nisha can afford.
Today, this little boy stands at a critical point in his journey. With timely surgery, his condition can be managed, and he can look forward to a healthier, brighter future. But without support, the risks are grave.
please help Baby of Nisha get the surgery he so urgently needs. Every contribution — big or small — brings him one step closer to survival and gives his brave mother the strength to keep fighting for her son.
Together, we can give this child a chance to live.
Pt. Baby of Nisha
|
BABY OF NISHA |
From the moment he was born in Lucknow, Baby of Nisha brought immeasurable joy to his parents. As their first and only child, he quickly became the center of their world — a bright, healthy newborn who filled their hearts with hope. For a while, everything seemed perfect.
However, just weeks after his birth, subtle but alarming signs began to emerge. His lips and nails started turning bluish — a possible sign of oxygen deficiency. His nails also began appearing broader and clubbed, and he developed troubling bowel issues. Deeply concerned, his parents rushed him to the hospital where he was born. After an initial assessment, the doctors suspected a congenital heart defect (CHD) and referred them for further testing.
Their fears were soon realized. The echocardiogram pointed toward a serious heart condition. The news was devastating, and tragically, Nisha’s husband could not bear the emotional shock. He passed away shortly after the diagnosis, leaving Nisha alone to care for their infant son. The baby was just 1.5 months old when he lost his father.
In the months that followed, Nisha’s world collapsed around her. She returned to her parental home, now the sole caregiver to her child while also depending on her elderly parents and supporting her younger, school-going sister. With no financial stability and her own grief weighing heavily on her, Nisha struggled to access the medical care her baby urgently needed. For over a year, his condition continued to deteriorate.
Eventually, Nisha brought him to KGMU Hospital in Lucknow, desperately seeking help. But despite her efforts, she found no solution. Just when all hope seemed lost, she met a compassionate hospital staff member named Mr. Gurmeet.
He guided her to Child Heart Foundation — and that meeting changed everything.
At the Child Heart Foundation in Delhi, under the expert care of Dr. Kohli, the baby underwent a thorough re-evaluation.
A fresh echocardiogram was performed, and the final diagnosis was confirmed:
Double Inlet Left Ventricle (DILV) with Large Inlet Ventricular Septal Defect (VSD) and Peri membranous Extension — a complex congenital heart defect where both atria drain into the same ventricle, impairing the heart’s ability to deliver oxygen-rich blood to the body.
Dr. Kohli confirmed that immediate surgical intervention is essential. The child now requires a two-stage treatment:
- Cardiac Catheterization (CATH)
- Glenn Shunt Surgery — a palliative procedure that improves blood flow to the lungs.
The cost of this life-saving treatment is approximately ₹4 lakhs — an amount far beyond what Nisha can afford.
Today, this little boy stands at a critical point in his journey. With timely surgery, his condition can be managed, and he can look forward to a healthier, brighter future. But without support, the risks are grave.
please help Baby of Nisha get the surgery he so urgently needs. Every contribution — big or small — brings him one step closer to survival and gives his brave mother the strength to keep fighting for her son.
Together, we can give this child a chance to live.
