Recently, a news story about a ‘college student abandoned as a child, now diagnosed with leukemia, searching for his biological family online’ has drawn widespread public attention. According to reports, the young man—just over 20 years old—was diagnosed with acute leukemia and, facing overwhelming medical costs and lacking any family support, turned to social media to seek help in finding his birth parents. He shared that he was abandoned as an infant and raised in a welfare institution, later supporting himself through college by working part-time jobs. Now struck by a life-threatening illness, he not only battles for survival but also struggles to access critical treatments like bone marrow matching due to the absence of immediate relatives. After the story went viral, netizens widely shared his plea and launched donation campaigns. Several charitable organizations have stepped in to assist with hospital coordination and fundraising. The case highlights gaps in social support for orphaned individuals after they reach adulthood and has reignited public discussion on healthcare access for rare diseases, bone marrow donation systems, and broader social safety nets. The student has begun initial treatment but continues to require ongoing support and attention.
近日，一则‘被遗弃大学生患白血病全网寻亲’的新闻引发广泛关注。据报道，一名20岁出头的大学生在确诊急性白血病后，因治疗费用高昂且无家人支持，被迫通过社交媒体公开寻亲。他自述从小被遗弃，由福利院抚养长大，成年后独自求学、打工维持生计。如今突遭重病打击，不仅面临生命威胁，更因缺乏直系亲属而难以进行骨髓配型等关键治疗。事件曝光后，众多网友纷纷转发求助信息，并发起捐款援助。部分公益组织也介入协助，为其联系医院、筹措医疗资金。该事件不仅折射出孤残儿童成年后的社会保障缺口，也再次引发公众对罕见病救助体系、骨髓捐献机制及社会关爱网络的深入讨论。目前，该学生已接受初步治疗，但后续仍需持续支持与关注。
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