Nityam is 10 years old.
At an age where children run without thinking, play without stopping, and live without fear, Nityam has always been a little more careful.
A little slower.
A little quieter.
Because since birth, his body has carried something unusual. What started as a slight swelling in his leg slowly became something much bigger. Something that people around him began to notice before he himself could understand it.
Today, that swelling has turned into what many in his village call “haathi jaisa pair” — an elephant-like leg.
But this is not just a physical difference.
Doctors have diagnosed Nityam with symptoms of lymphatic filariasis, a condition that causes severe swelling due to blockage in the lymphatic system. Over time, it can worsen, affecting movement, skin health, and overall quality of life.
And for Nityam, it is already getting worse.

When his parents first took him to a doctor years ago, they were told something that stayed with them.
“Let him grow a little older. Then treatment will be possible.”
So they waited.
They watched.
They hoped.
Years passed, and with every year, the swelling increased. What they thought would stay manageable slowly began to interfere with his daily life.
Walking became difficult.
Playing became limited.
And childhood… started shrinking.
Now, doctors have said clearly.
This is the time.
Treatment cannot be delayed anymore.

Nityam’s father is a labourer.
He leaves home every morning in search of work. Some days he finds it. Some days he returns empty-handed.
His earnings are never fixed.
His responsibilities are.
At home, Nityam’s mother takes care of everything. She is a housewife, managing the home, caring for her child, and silently carrying the weight of what lies ahead.
There are no savings.
No financial backup.
No plan for something this big.
Only a family trying their best with very little.

Doctors at SK Care Hospital, Raipur have advised a detailed and long-term treatment plan for Nityam.
His condition requires comprehensive medical evaluation including immunology and genetic assessment, followed by treatment with immuno-modulators, skin care management, treatment of secondary infections, and supportive surgical intervention if required.
This is not a quick fix.
It is a process.
A process that will take 2 to 3 months of continuous treatment, monitoring, and care.
The estimated cost of this entire treatment, including hospital stay, medicines, and support, is around ₹6,50,000.
For a family that struggles to meet daily needs, this amount feels impossible.

Nityam does not fully understand the medical terms.
He does not know what lymphatic filariasis means.
But he understands one thing.
He cannot do what other children do.
He cannot run freely.
He cannot play without being noticed.
He cannot ignore the way people look at his leg.
Sometimes, he just sits and watches others play.
Quietly.
His father does not say much.
But you can see it.
In the way he looks at his son.
In this way he hesitates when money is mentioned.
In this way he tries to stay strong, even when he knows he cannot arrange this treatment on his own.
Because no matter how hard he works…
This is beyond him.
This is not just about swelling.
This is about a child slowly losing the freedom of his own body.
This is about years of waiting turning into urgency.
This is about a family that did everything they could… and now needs help to do what they cannot.
Nityam has lived with this condition since birth.
He did not complain.
He did not ask for more.
He simply adapted.
But now, he needs a chance to live differently.
To walk without difficulty.
To play without hesitation.
To grow without this burden.
And sometimes, all it takes…
is someone deciding that a child’s life should not be limited by circumstances he never chose.

Hospital Estimate Documents
Note - Any amount raised beyond the required treatment cost will be used to support other individuals who were less fortunate and could not receive the help they needed.