Tanavvi Viij was diagnosed with spinal muscular dystrophy when she was just one year old. But even though it restricts her from many activities and moving across places, she wants to fulfil her plans of travelling and completing her studies.
“Please do register as a blood stem cell donor to help my son and other blood disorder patients like him.”
When Chhavi Rathore’s got to know about her son’s rare genetic disorder, she was devastates. After consulting multiple doctors and treatment sessions, her son recovered and is in a better state. Now, she wants to establish programs through which she could assist other parents facing similar dilemmas.
Sanya Sharma read about female genital mutilation when she was in her first year of law college. Today, through her project, ‘Scarlet Udaan’, she is working on normalising conversations on this topic.
Even though I was a technocrat all my life, I had a fervent passion and calling for literature.
Akshay Singh Chauhan was born with a deformed body and the doctors told at the time of his birth that he won’t be able to survive long. Although, he recovered over time and now works as an artist, writer and mental health activist.
Mohit Agarwal and Aditee Zanpure started teaching kids in a government school in Bengaluru. Overcoming initial struggles that they faced, they gradually learnt how to teach kids effectively. Now, they’re gearing up for online classes as the schools are shut due to the pandemic.
Ruthik Thorat is working as a student researcher with Mumbai-based HiMedia Laboratories on a novel drug that gives a pleiotropic effect for sickle cell anaemia.
Tanya Maheshwari suffered from Alopecia since she was 16. She faced social anxiety went into depression, but with time, she learnt to accept herself.
Every 5 minutes someone in India is diagnosed with blood cancer and other blood disorders.
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