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Rare Disease Day Event: Race For 7 2020

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Spinal Muscular Atrophy (SMA) – Deeksha Sampath

My Hurdles Hi, I am Deeksha Sampath, nine years old from Bangalore, suffering from a rare disease called SMA; it is killing all my physical abilities day by day. At...

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Spinal Muscular Atrophy (SMA) – Harsh

Spinal Muscular Atrophy (SMA) – Harsh...

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GBS FIGHTER FROM INDORE- Jeevan Kaneria

Hello friends, My name is  Jeevan Kaneria and i have been suffering from GBS (Gullian Barry Syndrome) in Indore, Madhya Pradesh India since April 1, 2016. This disease makes the...

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Spinal Muscular Dystrophy

Debosmita Ghosh...

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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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