Yashasvi Kalkade, a 14-year-old girl, has been diagnosed with Spinal Muscular Atrophy (SMA), a rare genetic neuromuscular disorder characterized by the degeneration of motor neurons in the spinal cord and lower brainstem. This progressive condition leads to muscle weakness, atrophy, and eventual loss of motor function.

Yashasvi's SMA has progressively worsened over the years, resulting in significant muscle weakness and loss of mobility. She is currently wheelchair-bound and requires assistance with activities of daily living. Additionally, Yashasvi has been experiencing worsening pain and discomfort on the left side of her rib cage for the past four years, which may indicate complications related to her SMA.

The recommended treatment for Yashasvi's SMA may involve a multidisciplinary approach aimed at managing symptoms, optimizing function, and improving quality of life. This may include:

Physical therapy and rehabilitation to maintain range of motion, prevent contractures, and improve strength.

Medications to manage symptoms such as pain, muscle spasms, and respiratory function.

Orthopedic interventions to address musculoskeletal complications such as scoliosis or joint contractures.

Close monitoring and management of respiratory function to prevent respiratory complications associated with SMA.

The cost of comprehensive treatment for SMA, including medical consultations, diagnostic tests, medications, rehabilitation therapies, and potential surgical interventions, can be substantial. It is estimated that the total cost for Yashasvi's treatment at SRCC Hospital, including procedures and postoperative ICU care, will be approximately 584,150 INR.

Yashasvi's father works as a vegetable vendor, earning a modest income to support the family. However, the cost of his daughter's medical treatment exceeds their financial means. Yashasvi's worsening condition and the additional expenses associated with her care have placed significant strain on the family's resources, making it difficult for them to afford the necessary medical interventions.

Given the dire financial circumstances faced by Yashasvi's family and the progressive nature of her condition, we earnestly request assistance in securing funding or resources to cover the cost of her medical treatment. Every effort will be made to ensure that Yashasvi receives the specialized care she urgently needs to manage her SMA and improve her quality of life.

Your support and assistance during this critical time will make a profound difference in Yashasvi's life and her family. We appeal to your compassion and generosity in helping to alleviate their financial burden and provide them with the hope and reassurance they need during this challenging journey.

Thank you for your attention to this matter. We remain hopeful for a positive response and deeply appreciate any assistance you may be able to provide.

All donations made to Saaya Foundation are exempt under section 80G of the Income Tax Act. Registered ID: U85300MH2022NPL383369

Saaya Foundation, a National Registered Charity is raising funds for Yashasvi Kalkade.

Saaya Foundation works in the areas of Medical Support, Women Empowerment, Child Rights, Social Awareness Programs, Protection from Domestic Violence, Health Initiatives, Personality Development Programs, Education, Natural Calamity Relief and other impact driven programs.