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Dr Srinivas Rao Nyapati

Obituary: Dr Nyapati Srinivasa Rao

By IORD | 0 comment
Being compassionate to the needs of rare disease patients has been a pet concern for late Dr Nyapati Srinivasa Rao, 61, in his long association with the Indian Organisation for Rare Diseases (IORD) as
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Now, Disability Certificate Only Through UDID Portal is Made Mandatory

By IORD | 0 comment
If you are a Rare Disease patient in need of a disability certificate, you may no longer need to face the hassle of going around offices as the Department of Empowerment of Persons with Disabilities (
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Union health ministry notifies National Policy for Rare Diseases 2021

Union Health Ministry Notifies National Policy for Rare Diseases 2021, Approves Rs 25 Cr Budget

By IORD | 0 comment
The Union Health & Family Welfare Ministry has officially approved the “National Policy for Rare Diseases 2021” on 30th March 2021.This development comes in the wake of the Delhi High court pullin
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IORD hosts webinar on ‘Rare Diseases Prevention’

By IORD | 0 comment
The Indian Organization for Rare Diseases (IORD) - a not-for-profit umbrella organisation - hosted a webinar on 'Rare Diseases: Prevention' with top global speakers on February 2, 2021.The topic assum
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Orphan Drugs To Get Govt. Support!

By IORD | 0 comment
In a reversal of turns, Orphan Drugs manufacturers in India may likely get some much needed relief from the proposed Rs 15,000 crore production linked incentive (PLI) scheme, according to latest news
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Telangana Health Minister Eatela Rajender Attends World Rare Disease Day in Hyderabad

By IORD | 0 comment
Source: Vaarthahttps://www.vaartha.com/telangana/ts-minister-etala-rajender-attends-world-rare-disease-day-event/
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Difficult To Identify Patient With Rare Disease

By IORD | 0 comment
Hyderabad: While there are 7,000 recorded rare diseases, it is an uphill task to identify a patient with a rare disease. As per the Indian Organization of Rare Diseases (IORD), it takes an average of
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Fund Woes Hit Rare Disease Patients

By IORD | 0 comment
Hyderabad: The draft of the National Policy for Rare Diseases introduced by the Union government on January 13, this year, was much debated in medical circles due to the suggestion of using crowdfundi
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Telangana Health Minister Eatala Rajender Says Need To Maintain Data On Rare Diseases

By IORD | 0 comment
Hyderabad: As much as 90 per cent of patients affected with rare diseases are from middle class, said Eatala Rajender, the Health Minister of Telangana, at the one-day conference on rare diseases here
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World Rare Disease Day 2020 in Hyderabad

By IORD | 0 comment
Telangana State Health Minister Eatela Rajender Attends World Rare Disease Day 2020 in HyderabadSource: Eenaduhttps://www.eenadu.net/latestnews/Etela-Speech-at-public-gardens-hyderabad/1600/120028427
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Rare Disease Day

IORD’s World Rare Disease Day-2020

By IORD | 0 comment
You are not alone as we all are one!Doctors, Survivors, Expert Speakers, Healthcare Staff, Patients' Organizations, Rare Disease Patients, Researchers, Policy Makers, Rare Disease Volunteers, Parents
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Hyderabad Observes World Rare Disease Day

By IORD | 0 comment
World Rare Disease Day was observed on Friday, here at HyderabadMillions of people around the world observe Rare Disease Day on the last day of February."Some rare diseases, such as cystic fibrosis, t
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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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Indian Organization For Rare Diseases
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  • Home
  • About Us
    • Management Committee
    • Advisory Board
    • Newsletters
    • Newsletter Subscription
  • Rare Diseases
  • Research
  • Services
  • Donate
  • Gallery
    • Photo Gallery
      • World Rare Disease Day – 2023
      • World Rare Disease Day 2020
    • Video Gallery
      • World Rare Disease Day – 2020
      • World Rare Disease Day – 2019
      • World Rare Disease Day – 2018
  • Blog
  • Contact Us
IORD – Indian Organization for Rare Diseases