Organization For Rare Diseases India

Organization For Rare Diseases India To empower rare disease patients and their families in India with access to national and international resources and help improve their quality of life.

Reach out for further enquiry on our ☎️ORDI National helpline number: 8892555000 Our Objectives
Rare Diseases Patients Helpline and Helpdesk: ORDI runs a national rare disease hotline (+91 8892 555 000) to hear the needs of rare disease patients. ORDI will setup a dedicated helpdesk with the goal of enabling patients, access to information and resources to guide them through the process of diagnos

ing and dealing with the rare conditions affecting their health and quality of life. ORDI develops and maintains a public website, a patient portal, organizes awareness campaigns, and an annual rare disease conference in India. Organize sponsored clinics that are at no cost to the rare disease patients by inviting national and international medical and research experts for selected rare diseases. The scope for this is enormous as there are 7000+ rare diseases and 70+ million patients in India. We will identify 5-10 diseases for the first couple years and coordinate clinics for them in metro cities with attendance by surrounding rural patients to the extent possible. Rare disease patient registry: Design, develop, maintain and make available, a registry of rare disease patients in India. Initially, this registry could be developed for a single or a group of rare diseases and eventually replicated to accommodate all rare diseases. This registry would be utilized for identifying patients for free/sponsored clinics, enrollment into clinical trials, broadcast important announcements, maintain patient informed consents to participate in special clinical research programs, etc. Biospecimen repository (bioBank) for rare diseases research: To enable the preservation of and utilization of biospecimens related to rare disease patients in India, ORDI shall provide a biobanking facility and enable access to researchers investigating rare diseases in India. These specimens are shared according to applicable laws and standard operating procedures (SOPs) relevant to human subjects research. Funding program for rare disease researchers in India: At least five competitive research awards based on external review to winning proposals. The biospecimens in the ORDI Biobank and the ORDI patient registry would be made available as resources to the grantees of these awards. ORDI will also catalyze relevant international collaborations for these grantees. For more visit: http://ordindia.in

10/08/2026

Bridging gaps in the Job Market: Building more inclusive opportunities for everyone.

Ruchita - Ruchita Sanchari asked a question many patients, doctors, caregivers, and genetics students may have but goes unaddressed and the answer is worth hearing.

Watch this important Q&A and join our upcoming interactive session - Every Wednesday on a new topic from 4:00-5:00 pm, where you can learn, ask questions, and be part of the conversation on rare disease care.

MedicalEducation

08/08/2026

Hear from our patients, caregivers and families about their experience at our recent CPR training session.

We’re planning our next CPR session and new community training programmes based on your needs.

👉Click the link in our bio to: Register your interest

We’ve listed a few topics to help parents and caregivers navigate everyday challenges with greater confidence. Please select the topics that would be most useful to you.
Your valuable feedback helps us create more meaningful support for the rare disease community.

Rare Info Series  #73 | Living with Neurofibromatosis: Challenges and Hope 💙Living with a rare condition comes with uniq...
07/08/2026

Rare Info Series #73 | Living with Neurofibromatosis: Challenges and Hope 💙

Living with a rare condition comes with unique challenges—but knowledge, support, and hope can make the journey easier. Join us for an insightful conversation on understanding life with Neurofibromatosis (NF) and the path towards better care and support.

🎙️ Speaker: Dr. Prabhudev Hiremath
Assistant Professor of Neurology / Paediatric Neurology, Ramaiah Hospital Bengaluru

🎤 Moderator: Dr. Aparna U Simha
Consultant Paediatrician, ORDI's Rare Clinic

📅 12 August 2026
🕓 4 PM – 5 PM IST
💻 Join via Zoom

Be part of the conversation and help build greater awareness around rare diseases. 💙

04/08/2026

When survival is at stake, every second counts.⏳🫀

A sneak peak into our CPR training day and the response we received.The real moments, the real voices, and the real impact was so very obvious to not hold it to ourselves but put it out here.

We’ll be sharing the full interviews soon, plus all the details about our next hands-on event, so follow along and don’t miss out.🙌🏻

🫀What if one simple skill could help you save a life?Our CPR and emergency response training  led by experts from Manipa...
03/08/2026

🫀What if one simple skill could help you save a life?

Our CPR and emergency response training led by experts from Manipal Hospitals Bengaluru who just didn’t teach us steps but gave our parents, caregivers and social workers the confidence to act when every second counts.

A heartfelt thank you to Dr. Shivakumar Shamarao ( a renowned Paediatrician) ,Dr Reshma Aramanadka (a pediatric intensivist) , Dr Reshma Ramesh and Mrs Santhanamari Manipal Hospitals Bengaluru for sharing their time, knowledge, and compassion with the rare disease community and beyond.

Once again, Thank you for empowering us!

🙋‍♀️Have you ever been in a situation where knowing CPR could’ve made a difference?

Double-tap if you believe everyone should learn this skill. 💚

# LifeSavingSkills

At the Apollo Genomics Institute Precision Health Series Rare Diseases Strategy, Mr Prasanna Shirol spoke about the need...
03/08/2026

At the Apollo Genomics Institute Precision Health Series Rare Diseases Strategy, Mr Prasanna Shirol spoke about the need for stronger state-level action on rare diseases.

He emphasised that health is a state subject and that every state should come forward with its own rare disease policy to build a sustainable model of care across the country.

His message was clear: real change depends not just on the right mindset but on the government's will to act.

📢 Rare Info Series | Session  #72Beyond medical treatment, quality care also depends on communication, empathy, guidance...
31/07/2026

📢 Rare Info Series | Session #72

Beyond medical treatment, quality care also depends on communication, empathy, guidance, and long-term support. Join us for an insightful session on "Non-medical Aspects of OI Care: Doctor's Contribution" and discover how healthcare professionals play a vital role in improving the lives of individuals with Osteogenesis Imperfecta (OI).

🎙 Speaker: Dr. Prashanth Inna
Consultant in Paediatric Orthopaedic Surgery, Rangadore Memorial Hospital & Bengaluru Manipal Hospitals, Old Airport Road, Domlur, Bengaluru.

🎤 Moderator: Ms. Krishnendu Menon
Business Development Manager, India & South Asia – Olink Proteomics, Thermo Fisher Scientific.

📅 Date: 05 August 2026
🕓 Time: 4:00 PM – 5:00 PM IST
📍 Platform: Zoom

Be part of this meaningful conversation and gain valuable perspectives on holistic care for the OI community.

There is nothing quite like practical learning, especially when it equips you with essential skills that may one day hel...
30/07/2026

There is nothing quite like practical learning, especially when it equips you with essential skills that may one day help save a life. Our CPR and emergency training day offered hands-on experience in understanding the techniques and mechanisms of administering CPR.

Through careful analysis and observation of clinical signs and body alignment. Dr Shivakumar Shamarao the entire team from Manipal Hospitals Bengaluru, trained us how to respond proactively in a medical situation. Patients, caregivers, and social workers from diverse rare disease communities and beyond came together, making the day not only productive but truly impactful.

SWIPE TO SEE OUR TRAINING DAY IN ACTION ➡️🫀

Poll Question:
“Do you wish to ORDI run more practical, hands-on workshops for the Rare disease community?”

On 25th July, Organization For Rare Diseases Indiahosted a hands-on CPR and emergency-response workshop with Manipal Hos...
28/07/2026

On 25th July, Organization For Rare Diseases Indiahosted a hands-on CPR and emergency-response workshop with Manipal Hospitals as our knowledge partner.

Caregivers, social workers, and patient advocates from the locality and the rare disease community joined for practical training because, in a medical emergency, the first few minutes matter most.

Dr Shivakumar Shamarao, Dr Reshma Aramanadka, Dr Reshma Ramesh, and Mrs Santhanamari from guided through hands-on steps of CPR
1. What to do,
2. How to do it, and
3. how to stay calm and act effectively.

For the families and caregivers who support people living with rare diseases, it is a skill that saves anyone's life, wherever you are.

Thank you to Manipal Hospitals for your expertise and to everyone who showed up ready to learn.

Some conversations can change millions of lives.On the 21st of July, our Founder & Executive Director, Prasanna Shirol, ...
27/07/2026

Some conversations can change millions of lives.

On the 21st of July, our Founder & Executive Director, Prasanna Shirol, was invited to a live panel on ET Now Swadesh with esteemed panellists involving Dr Rajeev Tandon and Dr Behram S Pardiwala, to speak on India's first clinically approved dengue vaccine - Qdenga by Takeda to make one point that matters deeply to us: a vaccine is only as powerful as it is reachable.

In a country where dengue touches lakhs of families every year, protection cannot be a privilege. Mr Prasanna Shirol carried the voice of patients and families into that room, advocating for the vaccine's inclusion in the NEML (National Essential Medicines List) as a temporary measure until legal approval of free supply of the vaccine for all citizens by the Government, so that price never stands between a family and their child's safety.

ORDI is privileged to be chosen as a part of an important discussion on national media and to speak for those too often left unheard. 🧡

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# 621, 4th Main, 10th A Cross, Mahalakshmipuram
Bangalore
560086

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