Authors of Blog – Harsha K Rajasimha MS, PhD – is a precision medicine data scientist and entrepreneur on a mission to accelerate human-centric clinical
Ayaansh a 2.5 years old boy needs Rs.16 crores to save his live. Sounds unbelievable, but the medicine available as a cure for a Rare
On 15th April 2021, the Annual International Pompe Day , Siva SK from Malaysia shares an awareness video about his daughter. This year’s theme is
On Parkinson’s Awareness Day sharing an article on Dr. Shanthipriya , founder and CEO of SAAR FOUNDATION , SHAKE OFF AND MOVE ON , WPC
We don’t choose the way we are born. But we can choose how to live our life. Here’s how I chose to live mine. My
A Team of Eight Persons with disabilities will scale Siachen Glacier, the highest battlefield in the World, said Major Vivek Jacob. The Indian Army has
OpenTreatments Foundation will enable treatments for genetic diseases regardless of rarity or geography using an open source software platform; Sanath Kumar Ramesh built the project
Vishal P.S.Palve , from Ahmednagar, Maharashtra, has completed B.Sc in Physics from Ferguson College and is currently a First Year M.Sc Physics Student of Pune
Miss Payel Bhattacharya, was diagnosed with a rare disease VHL or Von Hippel-Lindau. It is a genetic form of cancer. She is a Blogger at
Meet Tarun Kumar from Jaipur who sends in his story on how acceptance helped him to begin following his dreams and interests. He is one