+91-9666438880
indiaord@gmail.com
IORD – Indian Organization for Rare DiseasesIORD – Indian Organization for Rare DiseasesIORD – Indian Organization for Rare DiseasesIORD – Indian Organization for Rare Diseases
  • 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

Blog

Home Search results for "Indian Organisation For Rare Diseases" (Page 2)
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

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

IORD Initiates First-of-its-Kind Rare Disease Counting in Telangana

By IORD | IORD in News, IORD Updates, Rare Disease News | 0 comment | 16 November, 2022 | 0

Khammam: In a unique initiative to identify and count rare disease populations as part of a pilot study in Telangana, the Indian Organization for Rare Diseases (IORD) has started sensitization and interactive awareness meets with health workers in the Khammam district of Telangana. The pilot study – supported by Telangana state health commissioner Dr Sweta MohantyRead more

IORD Holds Rare Disease Awareness Workshop for Health Workers

IORD Holds Rare Disease Awareness Workshop for Health Workers

By IORD | IORD in News, IORD Updates, News | 0 comment | 12 November, 2022 | 0

Telangana: In the run-up to the implementation of the ground-breaking proposal to count rare disease patients within Telangana state, the Indian Organization for Rare Diseases (IORD) organised an awareness event on Rare Diseases for health workers including Accredited Social Health Activist (ASHA) members at Kamepally village in Khammam, Telangana on 10 November 2022. While addressing theRead more

Rare Diseases Policy Perspectives in India

Rare Diseases Policy Perspectives

By IORD | IORD Updates, News, Rare Disease News | 0 comment | 11 October, 2022 | 1

(This is an abridged version of the presentation delivered by Dr Kameshwar Rao, Executive Director, National Health Authority at the ‘Dr N Srinivasa Rao Memorial Symposium – Rare Diseases & Alternative Treatment’ organized by IORD at Hyderabad on 25th June.) Rare Diseases in Numbers: The World Health Organisation (WHO) estimates that there are an averageRead more

RARE DISEASES & ALTERNATE MEDICINE: Dr I. Rajyalakshmi

RARE DISEASES & ALTERNATE MEDICINE: Dr I. Rajyalakshmi

By IORD | IORD Updates, Rare Disease News | 0 comment | 23 September, 2022 | 1

(This is an abridged version of the presentation delivered by Dr I. Rajyalakshmi Homeopathy Practitioner, Hyderabad at the ‘Dr N Srinivasa Rao Memorial Symposium – Rare Diseases & Alternative Treatment’ organized by IORD at Hyderabad on 25th June) Rare disease: Definition The World Health Organization (WHO) defines a rare disease as a life-long debilitating diseaseRead more

Project Y and the Rare Care Centre at Perth, Australia, Children’s Hospital have partnered with the Indian Organisation for Rare Diseases (IORD) to improve rare disease visibility and recognition on a global scale

IORD Partnership: Counting Rare Disease Patients in Telangana State, India

By IORD | IORD Updates, Rare Disease News | 0 comment | 13 September, 2022 | 0

Project Y and the Rare Care Centre at Perth, Australia, Children’s Hospital have partnered with the Indian Organisation for Rare Diseases (IORD) to improve rare disease visibility and recognition on a global scale Following successful advocacy from IORD, the health commissioner of India’s state of Telangana approved a ground-breaking proposal to count rare disease patientsRead more

World Rare Disease Day 2022

IORD Takes Lead, Holds Series of Events to Mark World Rare Disease Day-2022

By IORD | IORD Updates | 0 comment | 25 February, 2022 | 0

The Indian Organization for Rare Diseases (IORD) is thrilled to call attention to the Word Rare Disease Day-2022 by organizing series of events to raise awareness about the issues of millions of Indians living with a rare disease. The World Rare Disease Day is observed every year on the last day of February (28th February).Read more

Ataxia Awareness Society

AAS to Host Webinar on Ataxia on 18 Dec

By IORD | Events | 0 comment | 14 December, 2021 | 0

The Ataxia Awareness Society (AAS) – an NGO dedicated to spread awareness about the rare disease, help the sufferers and encourage research in this field – is organising a webinar on Ataxia on 18th December (Saturday) at 7:30 PM IST. Being organised in collaboration with the Indian Organisation for Rare Diseases (IORD) & AAS, theRead more

123

Categories

  • ANI
  • Deccan Chronicle
  • Economic Times
  • Eenadu
  • Events
  • IORD in News
  • IORD Updates
  • News
  • Pharmabiz.com
  • Rare Disease News
  • Telangana Today
  • The Hans India
  • The Hindu
  • The Pioneer
  • Times Now
  • Times of India
  • Uncategorised
  • Vaartha

Recent Posts

  • My Battle with Porphyria: Why Jagruti Urges Nationwide Access to Hemin
  • May 2025: Rare Disease Updates, New Discoveries, Diagnostics, and Therapies
  • 78th WHA Takes Historic Step with Rare Diseases Resolution, 10-Year Global Plan Approved
  • India’s Rare Disease Crisis: Why Grassroots Solutions Are Urgently Needed
  • Advancing Rare Disease Awareness in India: Dr. Ramaiah Muthyala’s Strategic Insights

Archives

  • June 2025
  • May 2025
  • April 2025
  • March 2025
  • February 2025
  • January 2025
  • December 2024
  • November 2024
  • September 2024
  • July 2024
  • June 2024
  • May 2024
  • March 2024
  • February 2024
  • December 2023
  • October 2023
  • July 2023
  • June 2023
  • May 2023
  • April 2023
  • March 2023
  • February 2023
  • January 2023
  • December 2022
  • November 2022
  • October 2022
  • September 2022
  • August 2022
  • June 2022
  • May 2022
  • April 2022
  • March 2022
  • February 2022
  • January 2022
  • December 2021
  • November 2021
  • October 2021
  • September 2021
  • July 2021
  • May 2021
  • April 2021
  • November 2020
  • March 2020
  • February 2020
  • January 2020
  • February 2019
  • January 2018
  • September 2015

Follow Us

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.

RARE DISEASES

  • Rare Blood Diseases
  • Rare Heart Diseases
  • Rare Fungal Diseases
  • Rare Kidney Diseases
  • Rare Newborn Diseases
  • more...

SERVICES

  • Research
  • Let's Come Together
  • Partner With Us
  • Volunteers
  • Privacy Policy
  • Sitemap

CONTACT US

Indian Organization For Rare Diseases
Reg. Office (India): Plot 397, Road 22b, Jubilee Hills, Hyderabad (Telangana) 500033, Telangana, India

Phone: +91-9666438880

Email: indiaord@gmail.com

© 2020 Indian Organization For Rare Diseases | All Rights Reserved. Powered By Digital Dynamics
  • 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