The Apollo Centre of Genomic Medicine | Genomic Medicine in Delhi
The Apollo Centre of Genomic Medicine is a comprehensive integrated ‘state of the art’ specialist clinical genomic and genomic medicine services, led by world-renowned geneticist, supported by a highly skilled team of clinical geneticists, genetic counsellors, and genomic laboratory scientist. Genomic applications in clinical medicine and healthcare are rapidly changing the future of medicine.
The genome analysis of an individual gives the complete set of information about his/her DNA and RNA profiles which could be used in precision diagnosis, assessing inheritance risks, making reproductive choices, personalized treatment, long-term outcome, targeted health surveillance and adopting life style modifications.
Genomic medicine not only provides the family in precision diagnosis and treatment but also helps in the prediction, prevention and early detection for various genetic conditions. The centre aims to provide holistic care to the patients and family members through precision, personalized care, high level of prediction, facilitating prevention by pre-emptive approach and active participation.
About Us
A rare disease is a medical condition with a fairly low prevalence, specifically one that affects less than 65 out of every 100,000 individuals worldwide, according to the WHO. The very fact that we use the word ‘rare’ as part of the moniker ‘rare diseases’, is a form of alienation. In fact, rare diseases come under the broader category of Orphan diseases, which are diseases so rare that there is little to no funding and government support for them. Having a rare disease is very much like being an Orphan. Lost and set apart from the normal systems of society, with little support from institutions and governments.
Rare Humans of India is an attempt to overcome this otherness. A platform to voice previously unheard stories, a connection to patients in similar situations, and a way to make every single one with an Orphan disease feel cared for. What is left out of the official reports, the prescriptions and diagnostic tests, those form the stories to tell.
Rare Humans of India (RHoI) is centered on capturing and sharing the narratives of patients at Apollo Indraprastha, New Delhi, regarding their experiences with rare genetic disorders. This involves conducting interviews to gather insights into their challenges, advice, and stories, creating a platform for them to voice their concerns. RHoI aims to educate a wide audience and dispel misconceptions about these conditions while fostering empathy and support networks among patients with similar experiences. Additionally, its aims to create a platform that may be used to share information and advice, from other patients, doctors, and therapists, as well as contacts for the same, to better help patients deal with the social wellbeing challenges presented by such disorders. We also hope to provide information in regional languages across India to improve awareness, reduce stigma, and facilitate better healthcare outcomes through timely and accurate diagnoses.