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Newborn Screening – The Indian Perspective
We are incredibly excited to present to you Newborn Screening – The Indian Perspective by Dr. A. Radha Rama Devi.…
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In search of a correct diagnosis
In Search of the Right Diagnosis In 2008, one Sunday afternoon, in a city in Andhra Pradesh, Ravi, a three-year-old,…
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Farber disease: A rare disease that hurts the young
The pain afflicted by the devastating Farber disease is experienced by the whole family When they first heard his slightly…
Read MoreWhy is it important to engage rare disease stakeholders in India with global clinical research?
With a mission to educate, empower, and advocate for patients with rare diseases in the US and India, the Indo-US…
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Announcing IndoUSrare
Hi, I am Harsha Rajasimha, Founder and Chairman of IndoUSrare, an independent non-profit organization focused on helping patients with rare…
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A social entrepreneur on a mission to bridge the clinical research divide between the U.S. & India
Even as the world awaits a vaccine to tackle the global pandemic instigated by the novel coronavirus, there are over…
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Social entrepreneur on a mission to bridge the clinical research divide between the USA and India with advocacy and technology
Dr.Harsha Rajasimha is a rare disease social entrepreneur globally recognized for his work in genomics data science, persistent advocacy, and…
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