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On International Pompe Day, Pompe Foundation presents a captivating session on ‘Pompe: A rare disease”.

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On International Pompe Day, Pompe Foundation presents a captivating session on ‘Pompe: A rare disease”.

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With little support from the government, a faulty gene puts families with #Rarediseases in India, in a never-ending odyssey!

Meet the Pompe Warriors, 2 Different Lives, and their unique stories. They chose to thrive with passion, love, and hope besides surviving the error in #chromosome17. Watch the heart-rendering short...

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One of our Gaucher patient from Bengaluru who is on treatment now selected for Karnataka under 16 Cricket Team . What a proud moment for Rare Disease community

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Interview with Snigdha

Prasanna Shirol currently serves as the Co-founder & Executive Director of ORDI (Organization for Rare Diseases India), an Umbrella organization that represents 7000+ diseases in India. He has been instrumental...

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Watch how Mr. Shirol used his experience and knowledge in establishing rare disease centres in hospitals across India.

Prasanna Shirol whose daughter suffers from a rare disease called Pompe, used his experience and knowledge in establishing rare disease centres in hospitals across India. Click below link:...

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Racefor7 2021 Event

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RF7 2021 Bangalore

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Lalith suffering from pompe seeking treatment from Government

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