
10/07/2025
https://youtu.be/sZsUj7kmGuI?feature=shared
๐ง Understanding Spinal Muscular Atrophy (SMA)
Spinal Muscular Atrophy (SMA) is a rare, inherited neurological disorder that affects the motor neurons in the spinal cordโthose responsible for muscle movement. Caused by a deficiency of the SMN1 gene, SMA leads to progressive muscle weakness and can severely impact mobility, breathing, and swallowing, especially in infants diagnosed with Type 1 SMA.
While there is no complete cure, early diagnosis and intervention can make a significant difference. Today, advanced treatments such as gene therapy and medications like Spinraza, Zolgensma, and Evrysdi, along with physical therapy, offer hope and improved quality of life to those affected.
In this special episode of Uncondition Yourself with Namita Thapar, watch Namita in a heartfelt conversation with Dr. Neelu Desai, Paediatric Neurologist at P. D. Hinduja Hospital, Mumbai, as they shed light on SMAโits challenges, treatments, and the power of early care.
๐ฅ Donโt miss this enlightening discussion!
Spinal Muscular Atrophy (SMA) is a rare inherited disorder that affects the nerve cells (motor neurons) in the spinal cord responsible for controlling muscle...