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Home Search results for "rare disease awareness"
Dr. Anil Kumar Mandal, Senior Consultant Ophthalmologist at Centre for Sight, Banjara Hills, delivered a powerful keynote address at IORD’s World Rare Disease Day 2026.

Dr. Anil Kumar Mandal: 40-Year Journey Advancing Care in Congenital Glaucoma

By IORD | Rare Disease News, World Rare Disease Day 2026 | 0 comment | 8 April, 2026 | 0

This is a transcribed keynote address by Dr. Anil Kumar Mandal, Senior Consultant Ophthalmologist at Centre for Sight, Banjara Hills, delivered at the Indian Organisation for Rare Diseases (IORD) World Rare Disease Day 2026 event in Hyderabad, focusing on rare ophthalmic disorders.

Inaugural session of World Rare Disease Day 2026 conference in Hyderabad, with experts from IORD, LVPEI, and Rainbow Children’s Hospital

India: Rare Ophthalmic Disorders Take Centrestage at World Rare Disease Day-2026

By IORD | IORD in News, IORD Updates, Rare Disease News | 0 comment | 3 March, 2026 | 0

IORD marked World Rare Disease Day 2026 highlighting rare ophthalmic disorders, stressing early diagnosis, better referrals, and expanded genetic, multidisciplinary care with expert participation.

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

IORD emphasized the legal fraternity’s role in rare disease awareness, with Dr. Ramaiah Muthyala urging lawyers to support advocacy, patient rights, and public education initiatives.

Rare Disease Awareness in India Dr. Ramaiah Muthyala's Strategic Insights

Advancing Rare Disease Awareness in India: Dr. Ramaiah Muthyala’s Strategic Insights

By IORD | IORD in News, IORD Updates, Rare Disease News | 0 comment | 14 May, 2025 | 0

IORD CEO & President Dr. Ramaiah Muthyala provides insights on advancing rare disease awareness in India, stressing early diagnosis, frontline healthcare training, and integration into public health systems.

Prof. Ramaiah Muthyala (left, sitting) discussing innovative solutions for rare diseases at the 2025 World Orphan Drug Congress in Boston. With a focus on policy reforms and access to affordable medications, the panel addressed the urgent need for systemic change in rare disease care globally

Prof. Ramaiah Muthyala Calls for Policy Reforms at World Orphan Drug Congress-2025

By IORD | Events, IORD Updates, Rare Disease News | 0 comment | 4 May, 2025 | 0

IORD CEO and President Prof. Ramaiah Muthyala calls for policy reforms at the World Orphan Drug Congress 2025, addressing access barriers, costs, and solutions for rare disease care.

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

IORD marks World Rare Disease Day 2025 with a conference in Vijayawada, advocating policy action, improved diagnosis, treatment access, and greater awareness through expert and stakeholder participation.

This is a transcribed speech of Indian Organisation for Rare Diseases (IORD) President and CEO, Prof. Ramaiah Muthyala delivered at the World Rare Disease Day 2025 conference in Vijayawada, organized by the IORD.

Prof Ramaiah Muthyala: A Call for Policy Change and Rare Disease Healthcare in Andhra Pradesh

By IORD | Events, IORD Updates, Rare Disease News | 0 comment | 11 March, 2025 | 0

IORD CEO & President Prof. Ramaiah Muthyala calls for policy reforms in Andhra Pradesh, emphasizing improved rare disease healthcare, early diagnosis, and stronger government support for affected patients.

This extract is from a poster presented by Indian Organisation for Rare Diseases (IORD) President and CEO, Prof. Ramaiah Muthyala, titled: “Role of Patient Support Organizations and Collaborative Genomics Programs in Enabling Participatory Medicine for Rare Diseases in India: A Case Study of Autosomal Recessive Congenital Ichthyosis” at the Undiagnosed Disease Network Conference, South Korea (Sept 4–6, 2024).

Undiagnosed Disease Network Conference – Congenital Ichthyosis Case Study from India

By IORD | Uncategorised | 0 comment | 8 March, 2025 | 0

IORD CEO & President Prof Ramaiah Muthyala presents a case study on Autosomal Recessive Congenital Ichthyosis at the Undiagnosed Disease Network Conference, highlighting collaborative genomics and patient support in rare disease care.

Registration is now open for World Rare Disease Day-2025 Conference, organized by the Indian Organisation for Rare Diseases (IORD) at FORTUNE Murali Park, Vijayawada in Andhra Pradesh on 28 February, 2025

Registration is now open for IORD World Rare Disease Day-2025

By IORD | IORD Updates, Rare Disease News | 0 comment | 18 February, 2025 | 0

Registration open for IORD’s World Rare Disease Day 2025 conference in Vijayawada, aiming to advance innovation, collaboration, and solutions for rare disease diagnosis, treatment, and public health.

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).

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Recent Posts

  • Dr. Anil Kumar Mandal: 40-Year Journey Advancing Care in Congenital Glaucoma
  • World Rare Disease Day 2026: Dr. Ramaiah Muthyala Focuses on Rare Ophthalmic Disorders
  • 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

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