🚀 Exciting News from Rare Impact 2025! We are thrilled to welcome BIORx Venture Advisors, through their initiative Indian Healthcare Angels, as our latest partner in driving innovation, advocacy, and impact in the rare disease ecosystem. Register now: dakshamahealth.org/Hackathon.html

🌟 Hackathon teams = 8–12 changemakers! A mix of tech, health, design & patient voices. 🌍 Organizers group participants by country. #RareDisease #HealthTech #Hackathon Register now to participate: dakshamahealth.org/Hackathon.html

FAQ Spotlight! Support at Every Step! 🚀 💡 Expert mentors in all 3 phases! 🖥️ IT + logistics support (24/6)! 🏆 Jury-approved finalists may get mentorship + funding to pilot prototypes! Register now to participate: dakshamahealth.org/Hackathon.html

RARE IMPACT 2025- Thailand Country Lead Announcement We are delighted to introduce Ekawat Suwantaroj, Director of Thai Hemophilia Patient Club at the National Hemophilia Foundation of Thailand. Register now to be a part of Hackathon: dakshamahealth.org/Hackathon.html

🌍 Excited to introduce our Vietnam Country Lead for Rare Impact 2025 – Huy Do, President of the Vietnamese Organization for Rare Diseases. Let’s create meaningful change for people living with rare conditions. Register now to Participate: dakshamahealth.org/Hackathon.html

Did you know? Over 300 million people live with a rare disease - that’s nearly the population of the USA + UK combined! Rare is not small. Rare is global. Rare needs solutions. 👉 Register now: lnkd.in/gQn9WwPQ

🚨 Did you know? 95% of 7000+ rare diseases have no approved treatment. Rare Impact Hackathon 2025 invites innovators to rethink solutions- digital, low-cost, or repurposed. Be the change millions need. 🌍 Register now to Participate: dakshamahealth.org/Hackathon.html

Many kids with rare diseases never see adulthood. 💔 At #RareImpactHackathon2025, your ideas can change that—early diagnosis, patient support, new therapies. Innovate. Impact. Rewrite their future. Register now to Participate: dakshamahealth.org/Hackathon.html

Excited to welcome IndoUS Rare as a supporter for Rare Impact 2025! Their commitment to rare disease research and patient-focused initiatives will help drive innovation, collaboration, and real-world impact. Register now to Participate: dakshamahealth.org/Hackathon.html

💊 Treating rare diseases in India can cost up to ₹1 crore a year. Can tech + teamwork make care affordable? 💚 Join the mission: innovation meets compassion. Register now to Participate: dakshamahealth.org/Hackathon.html

We are thrilled to introduce Nadiah Hanim Abdul Latif as our Malaysia Country Lead for Rare Impact 2025! 🇲🇾 Register now to Participate: dakshamahealth.org/Hackathon.html

Rare disease patients wait 5–7 years for the right diagnosis, seeing 8 doctors & enduring misdiagnoses. What if AI, big data & community apps could cut that to months—or weeks? Join Rare Impact Hackathon 2025 (dakshamahealth.org/Hackathon.html) & help redefine diagnosis.

Rare diseases are called 'orphan diseases' because markets often overlook them. 🏥 At #RareImpactHackathon2025, you can build tech solutions, fundraising tools, or affordable therapies to transform lives. Register now to Participate: dakshamahealth.org/Hackathon.html

300 million people. One global call for equity.🌐 The UN recognized rare diseases - now let’s turn words into action. Join #RareImpactHackathon2025 to innovate for impact. Register now to Participate: dakshamahealth.org/Hackathon.html

1 in 2000 people lives with a rare disease but every story deserves support & compassion 💙 Join us at #RareImpact2025 Hackathon to co-create solutions that empower patients and families. Register now to Participate: dakshamahealth.org/Hackathon.html

We are proud to announce a new partnership between Rare Impact 2025 and Rare Diseases International (RDI)! Let’s make a rare impact — together. 💜 Register now: dakshamahealth.org/Hackathon.html

got a taste of UP administration today as we were sending life saving suplements for distribution at a cancer speciality hospital as charity. Sumit Tripathi mob num 8543949147 calls up to ask a bribe of Rs 50,000 Yogi Adityanath PMO India Brajesh Pathak

We are delighted to welcome APARDO as our newest partner for Rare Impact 2025 - an initiative dedicated to driving innovation, collaboration, and awareness in the field of rare diseases. Stay tuned as we move closer to Rare Impact 2025! Register now: dakshamahealth.org/Hackathon.html

Diverse health systems, shared challenges. Rare diseases affect 70M people in Asia-Pacific. #RareImpact2025 fosters cross-border collaboration to build innovative, tech-enabled solutions for the rare disease community. #RareImpact2025 #Hackathon #RareDiseases #PatientVoices

300 million people worldwide live with a rare disease. Rare may be unseen, but it is not unheard. This February, we raise our voices for awareness and visibility. #RareDiseaseDay #RareAwarenessMonth #RareButNotAlone