The discovery of CRISPR-Cas9 opened doors to explore the area of genomics in a new way. It shows the numerous possibilities to unlock the genome and lock it again through it’s highly specific and accurate nature. It’s major application in medical field as a therapeutic option for rare genetic disorders fascinated me a lot and thus, it became my area of research interest. Let’s deep dive into the fascinating world of CRISPR-Cas9 and explore the possibilities it holds. Discove

Lived Experience, Rights, and Responsibility I am a person with disability (PwD) diagnosed with Muscular Dystrophy , a rare neuromuscular genetic disorder classified under locomotor disability as per the Rights of Persons with Disabilities (RPwD) Act, 2016 . Muscular dystrophy is a progressive condition caused by the absence or dysfunction of essential muscle proteins, leading to muscle weakness and functional limitations. Living with a genetic condition from early childhoo