🌟 Spreading Awareness for Alagille Syndrome 🌟 This Alagille Syndrome Awareness Month, let’s shed light on this rare genetic disorder and support those affected. Together, we can inspire hope and foster understanding. 💚 #AlagilleSyndrome #RareDiseaseAwareness #SupportAndHope #ORDI Prasanna Shirol Madhana Gopal Praveen Kumar D S Sangeeta Barde Lalith Seetharaman #Advocacy #ORDI #RareDisease #Bengaluru #India #inspirational #nevergiveup #icareforrare #OrganizationforrarediseasesIndia #Awareness #Advocacy #Rarediseasepolicy #Treatment #Caregiver #Diagnosis #csrforrare
Organization for Rare Diseases India
Non-profit Organizations
Banglore, karnataka 2,117 followers
Collective voice of all persons living with rare disorders in India. National umbrella organization.
About us
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 diagnosing 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.
- Website
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https://ordindia.in/
External link for Organization for Rare Diseases India
- Industry
- Non-profit Organizations
- Company size
- 201-500 employees
- Headquarters
- Banglore, karnataka
- Type
- Educational
- Founded
- 2013
Locations
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Primary
Banglore, karnataka 560029 , IN
Employees at Organization for Rare Diseases India
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Prasanna Shirol
TEDxPune Speaker, Proud parent of Rare Disease Child, Rare Disease Advocate, Social Entrepreneur, Members ICMR - CECHR (Lay person), WHO-GCN4RD…
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Madhana Gopal
COO@ Organization for Rare Diseases India | #Rare Diseases Cause Volunteer forever |
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Madhumita Bhattacharya
Rare Disease Warrior | Counselling Psychologist | Mental Health Educator | Mental Health Professional | Promoting Mental Well-being and Awareness
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Purvi Shah
BGCI Level I certified Genetic Counselor
Updates
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Unleash your inner hero and be part of the change! 🌍 The #RaceFor7 is back for 2025 – a one-of-a-kind multi-city run/walk dedicated to raising awareness about rare diseases. 📅 Event Date: 23rd February 2025 ⏰ Time: 6:00 AM 📍 Location: Across multiple cities in India Every step you take helps amplify the voices of millions living with rare diseases. Together, we can create awareness and inspire hope. Prasanna Shirol Madhana Gopal Praveen Kumar D S Sangeeta Barde Lalith Seetharaman #RunForHope #ChangeMakers #MarathonForACause #RunForRare #RaceForAwareness #StepForChange #RareDiseaseRun #RunningForHope #Advocacy #ORDI #RareDisease #Bengaluru #India #inspirational #nevergiveup #icareforrare #OrganizationforrarediseasesIndia #Awareness #Advocacy #Rarediseasepolicy #Treatment #Caregiver #Diagnosis #csrforrare
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A rare disease doesn’t come with a manual; it comes with a mother who never gives up. 💪💖 #PrasannaShirol #MadhanaGopal #PraveenKumarDS #SangeetaBarde #lalithseetharaman #Advocacy #ORDI #RareDisease #Bengaluru #India #inspirational #nevergiveup #icareforrare #OrganizationforrarediseasesIndia #Awareness #Advocacy #Rarediseasepolicy #Treatment #Caregiver #Diagnosis #csrforrare
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May Makar Sankranti light up your life with new beginnings and endless happiness. Enjoy the festivities! #makarsankranti #pongal #bhogi #india #festival #culture #HappyMakaraSankranti #sankranti #india #lohri #kites #kitefestival #uttarayan #kiteflying #kite #instagram #indianfestival #winter
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𝐇𝐚𝐩𝐩𝐲 𝐌𝐚𝐤𝐚𝐫 𝐒𝐚𝐧𝐤𝐫𝐚𝐧𝐭𝐢 𝟐𝟎𝟐𝟓 | ಮಕರ ಸಂಕ್ರಾಂತಿಯ ಶುಭಾಶಯಗಳು. 𝐇𝐚𝐩𝐩𝐲 𝐌𝐚𝐤𝐚𝐫 𝐒𝐚𝐧𝐤𝐫𝐚𝐧𝐭𝐢 𝟐𝟎𝟐 #makarsankranti #pongal #bhogi #india #festival #culture #HappyMakaraSankranti #sankranti #india #lohri #kites #kitefestival #uttarayan #kiteflying #kite #instagram #indianfestival #winter
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Exploring disorders with symptoms similar to Moebius syndrome for accurate diagnosis and better management. Understanding the differences is key to effective care. #MoebiusSyndrome #RareDiseases #FacialParalysis #NeurologicalDisorders #DifferentialDiagnosis #rarediseaseawareness Prasanna Shirol Madhana Gopal Praveen Kumar D S Sangeeta Barde Lalith Seetharaman #Advocacy #ORDI #RareDisease #Bengaluru #India #inspirational #nevergiveup #icareforrare #OrganizationforrarediseasesIndia #Awareness #Advocacy #Rarediseasepolicy #Treatment #Caregiver #Diagnosis #csrforrare
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Facts About Moebius Syndrome 💜 It’s a rare neurological condition affecting facial expression and eye movement. Early intervention and therapies can improve quality of life. Awareness is the first step toward understanding and support! 🌟 #MoebiusSyndrome #RareDiseaseAwareness #SupportRareDiseases #knowledgeispower Prasanna Shirol Madhana Gopal Praveen Kumar D S Sangeeta Barde Lalith Seetharaman #Advocacy #ORDI #RareDisease #Bengaluru #India #inspirational #nevergiveup #icareforrare #OrganizationforrarediseasesIndia #Awareness #Advocacy #Rarediseasepolicy #Treatment #Caregiver #Diagnosis #csrforrare
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🌟 Understanding Moebius Syndrome 🌟 A rare condition affecting facial muscles and eye movement, Moebius Syndrome reminds us of the strength in every unique smile. Let’s spread awareness and support! 💜 #MoebiusSyndrome #RareDiseaseAwareness #SupportAndCare #uniquesmiles Prasanna Shirol Madhana Gopal Praveen Kumar D S Sangeeta Barde Lalith Seetharaman #Advocacy #ORDI #RareDisease #Bengaluru #India #inspirational #nevergiveup #icareforrare #OrganizationforrarediseasesIndia #Awareness #Advocacy #Rarediseasepolicy #Treatment #Caregiver #Diagnosis #csrforrare
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❌ Busting Myths, Building Awareness! ✅ Myth: Congenital Glaucoma can’t be treated. Truth: With early diagnosis and treatment, many children can lead healthy, normal lives. Let’s fight misinformation with facts! 💡👶💙 #CongenitalGlaucoma #MythBusting #EyeHealthAwareness #HealthyVision Prasanna Shirol Madhana Gopal Praveen Kumar D S Sangeeta Barde Lalith Seetharaman #Advocacy #ORDI #RareDisease #Bengaluru #India #inspirational #nevergiveup #icareforrare #OrganizationforrarediseasesIndia #Awareness #Advocacy #Rarediseasepolicy #Treatment #Caregiver #Diagnosis #csrforrare
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🔍 Understanding the Types of Congenital Glaucoma 👶💙 Did you know? Congenital Glaucoma can be categorized into Primary Congenital Glaucoma and Secondary Glaucoma caused by other conditions. Awareness leads to early diagnosis and better care! 🌟 #CongenitalGlaucoma #EyeHealth #VisionAwareness #HealthyEyes Prasanna Shirol Madhana Gopal Praveen Kumar D S Sangeeta Barde Lalith Seetharaman #Advocacy #ORDI #RareDisease #Bengaluru #India #inspirational #nevergiveup #icareforrare #OrganizationforrarediseasesIndia #Awareness #Advocacy #Rarediseasepolicy #Treatment #Caregiver #Diagnosis #csrforrare