Gargi suffers from hereditary transthyretin amyloidosis with polyneuropathy. This rare condition causes abnormal proteins to gather inside her peripheral nervous system.

This relentless buildup creates severe pain, constant numbness, and sudden muscle weakness. Once an incredibly active young woman, Gargi now struggles with basic daily tasks. Her mobility is rapidly declining, making it intensely difficult to enjoy the vibrant life she once knew in Jalgaon today.

Fortunately, innovative treatments like targeted gene therapies can stabilize these proteins and halt nerve damage. With your generous help, she can afford essential medicines and restore her beautiful independence forever.