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Battling for Genetic Counseling: The Promises and the Perils

Have we traveled far enough in understanding the importance of timely screening and the opinions of a genetic counselor; a profession that demands expertise in Empathy par Genetics? Dr. Dipanjana...

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Understanding Cilia and Ciliopathies

Who knew that a cell organelle as tiny as cilia could be involved in congenital heart disease and polycystic kidney disease? Dr. Sudipto Roy walks us through understanding cilia and...

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Championing the Odds, A Rare Talk by Avantika Shrivastava with DMD Warrior Dr. Sarthak Kamath.

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Chronic Pain: Its Physcological Impact and Coping Mechanisms

Chronic pain impacts daily lives and confidence; it creates anxiety for those who live with and around it. Acceptance, Awareness, and Empathy are very important. Join us with Dr. Anubha...

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Translational Readthrough: Making Sense Out Of Nonsense Mutations

Nonsense mutations are a causal factor of nearly 10% of genetic disorders. To make sense out of these nonsense mutations, we have Dr. Sandeep Eswarappa joining us in our ORDI...

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Home Ventilation In Children

What are the indications for the requirement of home ventilation? How do we go about it? Join us as Dr. Ilin Kinimi walks us through home ventilation in children through...

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Stream To End MS(Multiple Sclerosis)-Dialoque-How To Live With It

With adequate information, you can reduce the burden of MS with early diagnosis and treatment. Join us as Dr. Arvind Sharma walks us through Stream to deal with MS, Early...

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The Invisible link between Autism and Fragile X

With adequate information, it is possible to distinguish between Autism and Fragile X.Dr. Samir Hasan Dalwai & Shalini Kedia walk us through The invisible link between Autism & Fragile X...

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Congenital Muscular Dystrophy An Enigmatic Group of Disorders

Genetic Testing and Counseling should go hand in hand with a meticulous Clinical examination of inherited diseases, explains Prof  Nalini. To know more, join us as Dr. Nalini Atchayaram explains...

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Leveraging De Novo Proteomics For Biomarker Discovery For Rare Neurogenetic Diseases

Integrating metabolic biomarkers at the proteomic level will aid rare disease therapeutic research. Dr. Aditi Bhattacharya explains this, with reference to rare neurogenetic diseases through the ORDI Care For Rare...

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Upcoming Events

Our Executive Director Mr. Prasanna Shirol was a part of First Ever summit dedicated to advancing equitable care for rare diseases in older adults. The meeting was attended from 25 countries across Canada, Latin America, Europe, and Asia, representing patient and caregiver communities, patient advocates, healthcare professionals, and healthcare policy experts. This is a short video highlighting the impact of the initiative to date, in the words of the COLLABORATE Community.

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