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IORD & Rare Diseases in India: Impact, Initiatives & Challenges

IORD & Rare Diseases in India: Impact, Initiatives & Challenges

By IORD | IORD Updates, Rare Disease News | 0 comment | 5 December, 2024 | 0

Rare diseases, though affecting a small percentage of the population, represent a significant public health challenge in India. The Indian Organisation for Rare Diseases (IORD) has been at the forefront of advocating for policies, raising awareness, and improving treatment access. Rare diseases not only lead to the loss of human productivity but also place aRead more

IORD Webinar on Global Burden of Rare Diseases: Issues and Challenges

Registration Open for Webinar on Global Burden of Rare Diseases: Issues and Challenges

By IORD | Events, IORD in News, News | 0 comment | 19 November, 2024 | 0

Join an expert-led webinar exploring the complexities of rare diseases, featuring insights from IORD CEO & President Prof. Ramaiah Muthyala Rare diseases are a pressing global health issue, with an estimated 7,000 to 8,000 rare diseases identified worldwide. These conditions affect a relatively small percentage of the population, making awareness, diagnosis, and treatment especially challenging.Read more

Indian Organisation for Rare Diseases represented India at Rare Diseases International (RDI) Membership Meeting held on October 21-22, 2024, in Barcelona, Spain.

IORD Champions Rare Disease Advocacy at RDI Meeting in Barcelona

By IORD | IORD in News, IORD Updates, Rare Disease News | 0 comment | 2 November, 2024 | 0

The following excerpt is  from a presentation delivered by Krishnaji Rao Muthyala, Secretary of the Indian Organization for Rare Diseases (IORD), at the Rare Diseases International (RDI) Membership Meeting held on October 21-22, 2024, in Barcelona, Spain. Barcelona, Spain – There is a need for continued collaboration and innovation to create a more equitable healthcareRead more

The following is an excerpt from a panel discussion on Muscular Dystrophy by medical experts and members of BharathMD Foundation, a Parent Advocacy Organization of Muscular Dystrophy. The insights shared during this discussion highlight the importance of awareness, early diagnosis, and access to resources for families navigating the challenges of Muscular Dystrophy.

Muscular Dystrophy Complexities: Insights from Experts and Parent Advocacy Group

By IORD | IORD Updates, Rare Disease News | 0 comment | 19 September, 2024 | 0

The following is an excerpt from a panel discussion on Zee Telugu on Muscular Dystrophy featuring medical experts and members of the BharathMD Foundation, a parent advocacy organization for Muscular Dystrophy. The insights shared during this discussion highlight the importance of awareness, early diagnosis, and access to resources for families navigating the challenges of MuscularRead more

Indian Organisation for Rare Diseases (IORD) to host Indian Rare Diseases Nurses Network webinar on 8th August, 2024

IORD to Host Indian Rare Diseases Nurses Network Webinar on 8th August

By IORD | Events, IORD Updates, News | 0 comment | 19 July, 2024 | 0

Registration is Now Open for the Rare Diseases Nurses Network Webinar Hosted by the Indian Organisation for Rare Diseases (IORD). It will Highlight the Critical Role Nurses Play in Rare and Undiagnosed Diseases Worldwide.  Rare and undiagnosed diseases (RUD) have gained global recognition as a significant health priority following the United Nations (UN) Resolution onRead 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