Aarav's Journey
Early diagnosis gave Aarav the strength to fight SMA with hope.
We support children and families affected by Spinal Muscular Atrophy through awareness, expert connections, treatment support and a community that cares.
We are with families at every step of their SMA journey.
Support for fundraising and financial assistance for eligible families.
Support Now →Early diagnosis gave Aarav the strength to fight SMA with hope.
With the right care and support, Myra is living her dreams.
Together with doctors and donors, Vivaan is getting stronger.
Be the reason for a child's tomorrow.
Donate NowTogether we create impact and bring hope.
Spinal Muscular Atrophy (SMA) is a rare genetic disorder affecting motor neurons in the spinal cord, leading to progressive muscle weakness and loss of movement.
Early diagnosis and timely treatment can make a significant difference in the quality of life.
Learn MoreMost severe form. Symptoms appear within first 6 months.
Symptoms appear between 6–18 months. Children may sit but not walk.
Symptoms appear after 18 months. Children can walk but may lose ability.
Adult-onset SMA. Symptoms appear in late teens or adulthood.
Your organisation's CSR initiative can change the lives of SMA warriors and their families across India.
Become a CSR Partner →