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Indian Organization for Rare Diseases (IORD), a not-for-profit national advocacy organization, working for the cause of patients with rare diseases, spanning over the last fifteen years, hosted the awareness Bikeathon and Walkathon, to commemorate the World Rare Disease Day-2023, in association with the Government of Telangana.

Cycle For Rare: IORD’s Bikeathon, Walkathon for Rare Disease Draws Huge Response

By IORD | Events, IORD in News, IORD Updates, News, Rare Disease News | 0 comment | 9 March, 2023 | 0

The youngest Bikeathon participant was Korukonda lyosha, aged only eight years, while the oldest walkathon participant was Subhash Pande, aged 76 years at IORD’s Bikeathon │ Walkathon │ For Rare

World Rare Disease Day 2023

Cycle For Rare

By IORD | IORD in News, IORD Updates, News, Rare Disease News | 0 comment | 18 February, 2023 | 1

Join us to be the voice of 300 million affected people worldwide on World Rare Disease Day-2023. The not-for-profit Indian Organization for Rare Diseases (IORD) is excited to invite you all to an awareness bikeathon and walkathon being organised at the Necklace Road, Hyderabad on 26th February at 6.30 AM on Sunday.  Please register forRead more

Budget 2023: India Announces Elimination of Rare Sickle Cell Disease by 2047

Mission Mode: India to Screen 7 Crore Tribals for Sickle Cell Disease in 200 Districts

By IORD | Rare Disease News | 0 comment | 7 February, 2023 | 2

In a first of its kind comprehensive plan for management of any rare disease in India, the Union Finance minister Nirmala Sitharaman in her Budget 2023 presentation announced that the government would work on a mission mode for the elimination of the rare Sickle Cell Disease (SCD) from India by 2047. For this project, sheRead more

union health ministry notifies new centre of excellence for rare disease Treatment in kerala

Kerala’s SAT Hospital becomes 11th Centre of Excellence for Rare Disease Treatment

By IORD | IORD Updates, Rare Disease News | 0 comment | 20 January, 2023 | 0

The Union Health Ministry has designated Kerala’s Sree Avittam Thirunal Hospital (SAT) hospital, Government Medical College, Thiruvananthapuram, as a centre of excellence (CoE) for treating rare diseases, making it the 11th such hospital in the country under the Rare Disease Policy 2021.  The decision was formally taken by the Rare Disease Cell, Union Ministry of HealthRead more

Delhi High Court directs Centre to release Rs 5.35 crore to fund clinical trials for DMD

Delhi High Court directs Centre to release Rs 5.35 crore to fund clinical trials for DMD

By IORD | Rare Disease News | 0 comment | 27 December, 2022 | 0

The court direction – given on 22 December 2022 – came following a batch of petitions filed by parents of children suffering from rare diseases such as DMD and hunter syndrome. In a relief for scores of rare disease patients suffering from Duchenne Muscular Dystrophy (DMD) and Mucopolysaccharidosis II or MPS II (Hunter Syndrome) patients,Read more

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IORD

Indian Organization For Rare Diseases (IORD), a not-for-profit umbrella organization represents interests of all stakeholders of Rare Diseases in India including individual patients, patient support groups, health policy advocates and health care providers.

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Email: indiaord@gmail.com

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IORD – Indian Organization for Rare Diseases