ALS Advocate Cai Lei’s Powerful New Year Open Letter
ALS advocate Cai Lei shares a candid New Year’s open letter, revealing his health status and pushing for global ALS research breakthroughs.
Rare Diseases
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Cai Lei’s ALS Mission: Pushing Forward After Drug Mismatch
Despite a mismatch with the new Rag-17 ALS drug, Cai Lei leads research, funds studies, and trains families, showing resilience and inspiring the ALS community.
China’s Breakthroughs Shed Light on Rare Diseases ⚕️✨
China is revolutionizing how the world tackles rare diseases, reducing diagnosis times and boosting public awareness. Discover how these advancements are bringing hope to millions! ✨
China’s Healthcare Game-Changer: Rare Disease Medicines Now More Accessible 💊
China adds 13 new rare-disease drugs to its medical insurance catalog, making life-saving treatments more accessible and affordable to patients across the country. 👏💊
China Boosts Newborn Health Network to Beat Birth Defects 🐣
China is enhancing its newborn health network to prevent birth defects, with over 4,000 agencies now offering prenatal screenings and more initiatives boosting infant health. 🎉
Shanghai Sparks Hope at 2024 Global Rare Diseases Symposium 🌐💡
Shanghai hosts the 2024 Global Rare Diseases Symposium, uniting experts from the Chinese mainland and the U.S. to tackle rare diseases together.
Global Rare Diseases Symposium 2024 Kicks Off in Shanghai 🎉
Shanghai hosts the 2024 Global Rare Diseases Research Symposium, uniting experts worldwide to collaborate on rare diseases research and innovation.