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The only way forward is ZOLGENSMA VACCINE COSTING 17.50 Crore. Vaccine needs to be administered AS SOON AS POSSIBLE.
Anaahita just turned 6-month- she was diagnosed with spinal muscular atrophy type 1.
SMA is a rare genetic disorder that affects the nerve cells in the spinal cord, causing muscle weakness and wasting. This debilitating condition requires constant care and treatment and can have a significant impact on a child's ability to walk, stand, sit, and even breathe.
Anaahita's family is doing everything they can to help her, but the cost of her treatment is overwhelming. They are reaching out to the community for help with fundraising for her medical expenses.
Your support can make a real difference in Anaahita's life. Any donation, no matter how small, will help cover the cost of her treatment and provide her with the best possible chance of a bright future. Help us to achieve a milestone of 16crores for her treatment.
We hope you will consider making a donation to help Anaahita and her family. Together, we can make a real difference in her life.
Thank you for your generosity and support
Anaahita's family is doing everything they can to help her, but the cost of her treatment is overwhelming. They are reaching out to the community for help with fundraising for her medical expenses.
Your support can make a real difference in Anaahita's life. Any donation, no matter how small, will help cover the cost of her treatment and provide her with the best possible chance of a bright future. Help us to achieve a milestone of 16crores for her treatment.
We hope you will consider making a donation to help Anaahita and her family. Together, we can make a real difference in her life.
Thank you for your generosity and support
