On the occasion of International MPS Awareness Day 2026, Harivansh, Deputy Chairman, Rajya Sabha, launched the book “SHAURYA: A Father’s Promise” at Sir Ganga Ram Hospital, New Delhi, during a special event dedicated to raising awareness about Mucopolysaccharidosis (MPS) and rare diseases. Written by Saurabh Singh, Co-founder of the Rare Diseases India Foundation (RDIF), SHAURYA: A Father’s Promise tells the story of his son Shaurya, but echoes the pain, courage, and hope of millions of rare disease families around the world. Through Shaurya’s courageous battle with MPS II (Hunter Syndrome), the book gives voice to families who refuse to give up despite immense challenges and calls upon society to ensure that no child is forgotten simply because their disease is rare. At its heart is a father’s promise to transform his son’s courage into a lifelong mission for awareness, timely diagnosis, access to treatment, dignity, and hope for every child living with a rare disease. Though Shaurya left this world in 2025 at the age of 13, his courage lives on as a beacon of hope, inspiring a movement to ensure that no child with a rare disease is left behind. Beyond a personal story, the book sensitizes policymakers, decision-makers, healthcare stakeholders, and society at large to the urgent need for a comprehensive and effective National Rare Disease Policy that addresses the needs of all rare disease patients. It highlights the challenges faced by families in accessing timely diagnosis, treatment, and support, while advocating for equitable healthcare, stronger policy interventions, and a more compassionate ecosystem for rare disease communities. Speaking on the occasion, Harivansh, Deputy Chairman, Rajya Sabha, acknowledged the extraordinary dedication of Saurabh Singh, Co-Founder of the Rare Diseases India Foundation (RDIF), who left a promising career in a multinational company to devote his life to the cause of rare disease patients and their families across India. He remarked that Saurabh transformed his personal struggle into a national mission, turning pain into purpose and becoming a powerful voice for thousands affected by rare diseases. Appreciating the impactful work of RDIF, Harivansh noted that Saurabh Singh’s commitment, compassion, and perseverance have helped bring the concerns of the rare disease community to the forefront of public awareness and policymaking. He emphasized that the voices of MPS and other rare disease patients must be heard at the highest levels of governance and that collective efforts are needed to ensure dignity, care, and hope for every affected family. The event was organized by the Rare Diseases India Foundation (RDIF) in association with Sir Ganga Ram Hospital, New Delhi, bringing together leading voices from the medical, scientific, and rare disease communities, including Dr. Ratna Dua Puri of Sir Ganga Ram Hospital, Dr. Madhulika Kabra of ICMR, Dr. Neerja Gupta of AIIMS New Delhi, Dr. Sunita Bijarnia, Dr. Veronica Arora, and Dr. Swasti Pal, who shared valuable insights on the challenges, advancements, and future priorities in the field of rare diseases. The occasion was also graced by the leadership of Sir Ganga Ram Hospital, including Dr. D. S. Rana, Chairman, Sir Ganga Ram Trust Society and Sir Ganga Ram Hospital; Dr. Ajay Swaroop, Chairman, Board of Management; Dr. Jaya Sood, Vice Chairperson, Board of Management; and Dr. A. K. Bhalla, Honorary Secretary and Director, Sir Ganga Ram Hospital. They were joined by eminent clinicians, researchers, patient advocates, policymakers, and rare disease families, reaffirming a collective commitment to improving the lives of those affected by rare diseases.End of ArticleFollow Us On Social MediaVideosAfter TCS Nashik Case, Ex-Wipro Pune Employee Alleges Religious Conversion, Forced ResignationNo Woman In Karnataka Cabinet: Margaret Alva ‘Deeply Disappointed’ Over DK Shivakumar Oath CeremonyPune IT Firm Abruptly Closes Operations, Over 700 Employees And Interns Left JoblessCongress Tells Cadre To Ignore CJP, Stay Focused On NEET-CBSE AgitationWhy IRCTC Is Verifying 6 Crore Users And Deploying AI Cameras In 800 KitchensBeyond Roads And Troops: Why India Is Building A Model Village Near The LACBJP Alleges TMC MLA Linked To Land Grab, Compensation Fraud And Illegal Construction; Seeks ED ProbeBihar Hospital Fire Claims Four Lives; CM Announces Rs 4 Lakh AidViral Marriage Proposal By Army Captain Draws Scrutiny Over Military ProtocolPermission Pending As CJP Mobilises Supporters For June 6 Jantar Mantar Protest123Photostories8 words that women hate from the core of their heart: Which one can YOU not standGetting married soon? 10 common questions women should ask themselves before tying the knotMillions of women live with period pain, PMOS and UTIs: But experts say that doesn’t make them normalFrom Spiti to Antarctica: World’s most unusual post offices every traveller should visitToo much screen time? 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On the occasion of International MPS Awareness Day 2026, Harivansh, Deputy Chairman, Rajya Sabha, launched the book “SHAURYA: A Father’s Promise” at Sir Ganga Ram Hospital, New Delhi, during a special event dedicated to raising awareness about Mucopolysaccharidosis (MPS) and rare diseases. Written by Saurabh Singh, Co-founder of the Rare Diseases India Foundation (RDIF), SHAURYA: A Father’s Promise tells the story of his son Shaurya, but echoes the pain, courage, and hope of millions of rare disease families around the world. Through Shaurya’s courageous battle with MPS II (Hunter Syndrome), the book gives voice to families who refuse to give up despite immense challenges and calls upon society to ensure that no child is forgotten simply because their disease is rare. At its heart is a father’s promise to transform his son’s courage into a lifelong mission for awareness, timely diagnosis, access to treatment, dignity, and hope for every child living with a rare disease. Though Shaurya left this world in 2025 at the age of 13, his courage lives on as a beacon of hope, inspiring a movement to ensure that no child with a rare disease is left behind. Beyond a personal story, the book sensitizes policymakers, decision-makers, healthcare stakeholders, and society at large to the urgent need for a comprehensive and effective National Rare Disease Policy that addresses the needs of all rare disease patients. It highlights the challenges faced by families in accessing timely diagnosis, treatment, and support, while advocating for equitable healthcare, stronger policy interventions, and a more compassionate ecosystem for rare disease communities. Speaking on the occasion, Harivansh, Deputy Chairman, Rajya Sabha, acknowledged the extraordinary dedication of Saurabh Singh, Co-Founder of the Rare Diseases India Foundation (RDIF), who left a promising career in a multinational company to devote his life to the cause of rare disease patients and their families across India. He remarked that Saurabh transformed his personal struggle into a national mission, turning pain into purpose and becoming a powerful voice for thousands affected by rare diseases. Appreciating the impactful work of RDIF, Harivansh noted that Saurabh Singh’s commitment, compassion, and perseverance have helped bring the concerns of the rare disease community to the forefront of public awareness and policymaking. He emphasized that the voices of MPS and other rare disease patients must be heard at the highest levels of governance and that collective efforts are needed to ensure dignity, care, and hope for every affected family. The event was organized by the Rare Diseases India Foundation (RDIF) in association with Sir Ganga Ram Hospital, New Delhi, bringing together leading voices from the medical, scientific, and rare disease communities, including Dr. Ratna Dua Puri of Sir Ganga Ram Hospital, Dr. Madhulika Kabra of ICMR, Dr. Neerja Gupta of AIIMS New Delhi, Dr. Sunita Bijarnia, Dr. Veronica Arora, and Dr. Swasti Pal, who shared valuable insights on the challenges, advancements, and future priorities in the field of rare diseases. The occasion was also graced by the leadership of Sir Ganga Ram Hospital, including Dr. D. S. Rana, Chairman, Sir Ganga Ram Trust Society and Sir Ganga Ram Hospital; Dr. Ajay Swaroop, Chairman, Board of Management; Dr. Jaya Sood, Vice Chairperson, Board of Management; and Dr. A. K. Bhalla, Honorary Secretary and Director, Sir Ganga Ram Hospital. They were joined by eminent clinicians, researchers, patient advocates, policymakers, and rare disease families, reaffirming a collective commitment to improving the lives of those affected by rare diseases.
