A Mother’s Appeal: Help My Baby Kabbir Fight Spinal Muscular Atrophy
My name is Ishita, and I am writing this with a mother’s trembling hands and a heart full of hope. After 5 years of marriage, God blessed us with the most precious gift of our lives — our baby boy, Kabbir. He brought endless joy, laughter, and dreams into our home.
But just 6 months into his life, those dreams have been shattered by a cruel diagnosis — Spinal Muscular Atrophy (SMA) Type 1.
SMA is a rare genetic disorder that weakens the muscles and makes even the simplest acts — breathing, swallowing, or moving — a daily struggle. Every single day feels like a battle against time.
Doctors have told us that there is only one hope for Kabbir: Zolgensma Gene Therapy. This one-time infusion can stop the progression of the disease and give our baby a chance at a normal life. But the cost of this miracle treatment is something no parent can ever be prepared for — ₹16+ Crore INR
We are ordinary parents, not capable of raising such an unimaginable amount on our own. Every passing day, every delayed treatment reduces our chances of saving Kabbir.
💔 As a mother, it breaks me to see my child fighting for breath when all I want is to see him take his first steps, say his first words, and live a life filled with love and laughter.
🙏 I am humbly appealing to you — your kindness can save my son’s life. No contribution is small; each rupee brings us closer to giving Kabbir the future he deserves.
Please help us by:
- Donating whatever you can towards Kabbir’s treatment.
- Sharing this fundraiser with your friends, family, and network.
Together, we can give my baby boy a second chance at life.
💙 From one parent’s heart to another — I beg you, please stand with us in this fight for Kabbir’s life.
With gratitude and hope,
Ishita (Mother of Kabbir)
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.
