Archive · 23 Jul 2025
2-Year-Old Fighting SMA Needs ₹16 Crore Treatment
Kaashvi is a little girl who is very sick because of a disease called SMA.
This disease makes it hard for her muscles to work.
Doctors have a special medicine called Zolgensma that can help her, but she needs to get it before her third birthday.
The medicine costs a lot of money, about ₹16 crore!
Her family is asking for help from anyone who can donate to help her get better and live a healthy life.
Kaashvi, a 2.8-year-old girl, is battling Spinal Muscular Atrophy (SMA) Type 2.
Doctors recommend a one-time gene therapy, Zolgensma, to be effective.
The treatment must be administered before her third birthday.
The life-saving injection costs ₹16 crore.
Her family is appealing to the public for urgent financial help.
- Who
- Kaashvi, a 2.8-year-old girl with Spinal Muscular Atrophy (SMA) Type 2, and her parents.
- What
- Kaashvi needs a ₹16 crore gene therapy called Zolgensma to treat her Spinal Muscular Atrophy.
- When
- Treatment needs to be done before Kaashvi's third birthday.
- Where
- Kaashvi's family is currently in Bengaluru.
- Why
- To combat SMA Type 2, a severe genetic condition that weakens her muscles.
- Patient
- Kaashvi
- Age
- 2.8 years old
- Condition
- Spinal Muscular Atrophy (SMA) Type 2
- Treatment
- Zolgensma gene therapy
- Treatment Cost
- ₹16 crore
- Treatment Deadline
- Before 3rd birthday