Power In Me Foundation
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We work for the rights of the people with rare disease pan India level, creating awareness and empowering the rare community
✨ BIG NEWS! ✨
We’ve hit a massive milestone! Power In Me Foundation is now officially registered with NITI Aayog (NGO DARPAN) with ID: DL/2026/1136689! 📜🎉
What does this mean? More transparency, stronger government alignment, and a massively amplified capacity to serve the Rare Disease community right where it matters most—at the ground level.
We are fully geared up for high-impact collaborations:
🔹 CSR-1 Registered 💼
🔹 80G & 12A Certified (Tax exemptions on all donations!) 💰
💡 How you can help:
Whether you are a corporation looking for a trusted CSR partner or an individual who wants to make a real difference, your funding can transform lives. Rare diseases require immense resources, continuous advocacy, and deep ground-level support. Let's join forces!
🔗 Get in touch to donate or collaborate:
🌐 www.powerinme.org
📧 [email protected]
👉 Drop a 🙌 in the comments to celebrate this milestone with us!
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Can technology bring better healthcare closer to home? 🏡✨
For patients dealing with rare diseases in rural India, getting the right diagnosis takes years. We built Pathfinder AI to change that.
As the Winner of the International Rare Impact Hackathon 2025, Pathfinder AI doesn't just fast-track diagnosis—it puts the power back in the patient’s hands. By allowing users to rate and review local hospitals, doctors, and pathologies, we are helping families in remote areas make informed, life-saving healthcare decisions close to home. 📊❤️
To take this from an award-winning innovation to the ground, Power In Me Foundation is launching a critical pilot project. We are looking for CSR partnerships, corporate sponsors, and donations to scale this impact and connect village communities directly to specialist networks and clinical research. 🤝🚀
🔒 Why Partner With Us?
We are a fully verified, compliant trust with active CSR1, 80G, and 12A certifications. Your corporate contributions qualify under Schedule VII (Companies Act, 2013) for:
🔹 Clause (i): Health Care & Preventive Health
🔹 Clause (x): Rural Development
🔹 Clause (ix): Tech & Medical R&D
Let's collaborate to map a healthier, more equitable future.
📥 How to Support: Click the link in our bio to donate, or DM us to collaborate on a CSR initiative!
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26/06/2026
Delayed treatment = Irreversible damage. Early treatment = Full independence. 🩸💪
Take a look at the infographic. For individuals with Hemophilia, a delay in accessing clotting factors initiates a painful countdown:
1️⃣ Massive internal joint bleeding ➡️
2️⃣ Musculoskeletal erosion & cartilage damage ➡️
3️⃣ Permanent ankylosis & loss of independence.
But it doesn't have to be this way! Early Prophylaxis (scheduled infusions) completely changes the narrative, securing joint health and a life of full mobility.
For 'Year of Rare' 2026, Power In Me Foundation is on a mission to ensure no one loses their mobility to a treatable condition. But we cannot do it alone. We need YOU!
❤️ How You Can Help:
💰 CSR Funding & Corporate Partners: We are CSR1, 80G, and 12A certified. Partner with us to channel corporate resources where they matter most.
🙋♂️ Volunteer: Join our community to support patient care and spread vital awareness.
🔄 Share This Post: A simple reshare to your story could connect us with a donor, volunteer, or corporate sponsor who can save a life!
✨ Act Now: Scan the QR code in the image to donate, or drop us a DM to volunteer!
📞 Contact: 8851537816
🌐 Follow: Power In Me Foundation
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Contact the organization
Telephone
Website
Address
Laxminagar
Delhi
110092
Opening Hours
| Monday | 11am - 7pm |
| Tuesday | 11am - 7pm |
| Wednesday | 9am - 5pm |
| Thursday | 9am - 5pm |
| Friday | 9am - 7pm |
