Mr. Cai Lei is a well-known Chinese entrepreneur and former vice president of JD.com. Since his diagnosis with amyotrophic lateral sclerosis (ALS), commonly known as ‘Lou Gehrig’s disease,’ in 2019, he has actively championed ALS research and patient support initiatives. Recent public updates indicate that his condition has progressed to a near-terminal stage, with severely limited physical function. Nevertheless, using eye-tracking technology, he continues to work and advocate for rare disease research. ALS is a progressive neurodegenerative disorder that gradually robs patients of motor control, eventually impairing respiratory function. While there is currently no cure globally, Cai has significantly raised public awareness by establishing the ‘ALS Fund’ and accelerating drug development platforms in China. His resilience and dedication have inspired countless families affected by ALS and mobilized greater societal resources toward rare disease research. Despite his deteriorating health, Cai remains resolute: ‘As long as I have one breath left, I will keep fighting.’ His actions embody the dignity and strength of life under extreme adversity.
蔡磊先生是中国知名的企业家和前京东副总裁，自2019年被确诊患有肌萎缩侧索硬化症（ALS，俗称‘渐冻症’）以来，他始终积极投身于ALS的科研推动与患者援助事业。据近期公开信息显示，蔡磊的病情已进展至接近终末期，身体功能严重受限，但仍通过眼动设备坚持工作，继续为推动罕见病研究发声。ALS是一种进行性神经退行性疾病，会逐渐剥夺患者的运动能力，最终影响呼吸功能。目前全球尚无治愈手段，但蔡磊通过创立‘渐冻人基金’、推动药物研发平台建设等方式，极大提升了公众对这一罕见病的关注度，并加速了国内相关科研进程。他的坚韧与奉献精神，不仅激励了无数患者家庭，也促使更多社会资源投入到罕见病领域。尽管病情日益恶化，蔡磊仍表示‘只要还有一口气，就要战斗到底’，其行动彰显了生命在极限状态下的尊严与力量。
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