My name is Naveena, and I write this with trembling hands and a heart full of hope.

God blessed us with our precious baby boy, Aryansh — a bundle of joy who brought laughter, dreams, and love into our lives. But just 1 year and 8 months into his life, our world was turned upside down with a heartbreaking diagnosis:

Spinal Muscular Atrophy (SMA) Type 2.

SMA is a rare genetic disorder that weakens muscles and makes even the simplest actions — like breathing, swallowing, or moving — a daily struggle. Each day is a race against time.

Doctors have told us that there is only one hopefor Aryansh:

Zolgensma Gene Therapy — a one-time infusion that can stop the progression of SMA and give him a chance at a normal life.

But the cost of this life-saving treatment is beyond our means:

?1.5 Crores (INR) it’s an unimaginable amount for us as ordinary parents.

Every single day we wait, Aryansh’s chances of survival diminish. As a mother, it breaks me to see my child struggling for breath when all I want is to see him take his first steps, speak his first words, and live a life full of joy.

I am humbly appealing to your heart. Your kindness can save my baby’s life.

No amount is too small — every rupee brings us closer to giving Aryansh the future he deserves.

Here’s how you can help:

1. Donate whatever you can to support Aryansh’s treatment
2. Share this message or fundraiser with your friends, family, and network

Together, we can give Aryansh a second chance at life.

???? From one parent’s heart to another — I beg you, please stand with us in this fight.

With gratitude and hope,

Naveena

(Mother of Aryansh)

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