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Home Search results for "Indian Organization for Rare Diseases"
In this interview with ABN Andhra Jyothi channel, Dr Ramaiah Muthyala highlights IORD’s journey, contribution, key milestones, advocacy roles, challenges and impact.

How IORD Spurred Major Policy Shifts and Community Awareness

By IORD | ABN Andhra Jyothi, IORD Updates, Rare Disease News | 0 comment | 7 August, 2025 | 0

Learn how IORD, led by Dr. Ramaiah Muthyala, influenced national policy, raised awareness & advanced patient advocacy across India

Dr. Ramaiah Muthyala addressed the Khammam Bar Association, highlighting the legal community’s role in rare disease advocacy and patient rights.

Legal Fraternity’s Role Vital in Rare Disease Awareness: Dr. Ramaiah Muthyala

By IORD | IORD in News, Sakshi | 0 comment | 16 July, 2025 | 0

Khammam: Dr. Ramaiah Muthyala, President of the Indian Organization for Rare Diseases (IORD), addressed the Khammam Bar Association at an awareness program on “Rare Diseases – Role of Legal Professionals”, held at the District Bar Association Hall on Tuesday.   He emphasized the critical role that legal professionals play in raising awareness about rare diseases andRead more

Closing Critical Gaps in India's Rare Disease Framework: A Vision from Dr. Ramaiah Muthyala

From Policy to Patients: Addressing Gaps in Rare Disease Care

By IORD | IORD in News, News, Rare Disease News | 0 comment | 13 May, 2025 | 0

The following is an excerpt from a three-part interview series featuring IORD CEO & President Prof. Ramaiah Muthyala. In the first part, he speaks to Health Issues India on rare disease care in India and highlights NPRD’s progress, persistent gaps in diagnosis, treatment, and the need for disease-specific approaches. Read more at healthissuesindia.com   RareRead more

Prof. Ramaiah Muthyala, CEO & President of IORD, inaugurates the World Rare Disease Day 2025 conference in Vijayawada by lighting the ceremonial lamp in the presence of dignitaries.

World Rare Disease Day 2025: IORD Advocates for Policy & Awareness

By IORD | Events, IORD Updates, Rare Disease News | 0 comment | 19 March, 2025 | 0

Vijayawada: The Indian Organization for Rare Diseases (IORD), a non-profit advocacy body, convened a critical conference titled “RAISE THE AWARENESS – RARE DISEASES: Advocate Public Policy, Promote Diagnosis, Treatment & Social Services” at Fortune Murali Park, Vijayawada on February 28, to mark World Rare Disease Day 2025.   The event, attended by healthcare experts, policymakers,Read more

The Global Burden of Rare Diseases: Issues and Challenges' was addressed by Hyderabad-based Indian Organization for Rare Diseases founder Prof. Ramaiah Muthyala.

Affordability of drugs for rare diseases a challenge

By IORD | IORD in News, Times of India | 0 comment | 21 December, 2024 | 0

The following article is reproduced from a news article by Amrita Didyala, published in Times of India on Wednesday, December 18, 2024, based on the webinar ‘The Global Burden of Rare Diseases: Issues and Challenges’ addressed by Prof. Ramaiah Muthyala at the Federation of Asian Biotech Associations (FABA)-US Chapter. Hyderabad: Speaking at a webinar onRead more

A webinar organised by the Federation of Asian Biotech Associations-US chapter highlighted the socio-economic and emotional toll on the 70 million Indians affected by rare diseases (RDs)

Webinar Highlights Challenges Presented by Rare Diseases

By IORD | Deccan Chronicle, IORD in News | 0 comment | 21 December, 2024 | 0

A webinar organized by the Federation of Asian Biotech Associations-US chapter highlighted the socio-economic and emotional impact on the 70 million Indians affected by rare diseases (RDs).

Minnesota legislature introduces bipartisan bill designating August 15 as India Day, celebrating 50,000 Indian-Americans' contributions.

Minnesota Legislature Introduces Historic Bill Designating August 15 as India Day

By IORD | Events, IORD in News, IORD Updates | 0 comment | 15 August, 2021 | 0

State Senate Leaders Join Community Campaign Celebrating Indian-American Contributions Minnesota, August 15, 2021: In a remarkable move, the Minnesota State House and Senate have come together to introduce bipartisan legislation that officially marks August 15 as India Day. This initiative acknowledges the vital contributions of Indian Americans in the state and offers a platform toRead more

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Recent Posts

  • India: Rare Ophthalmic Disorders Take Centrestage at World Rare Disease Day-2026
  • IORD to Host World Rare Disease Day 2026 Conference Focused on Rare Ophthalmic Conditions
  • Bridging India’s Rare Disease Treatment Gap Through Public-Interest Pharmaceuticals
  • India Steps Forward as a Global Leader in Rare Disease Management
  • From Hope to Action: IORD Calls for Inclusive Global Action on Rare Diseases

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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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Plot No. 397, Road No. 22B, Jubilee Hills, Hyderabad – 500033, Telangana, India.

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Email: indiaord@gmail.com

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IORD – Indian Organization for Rare Diseases