{"id":8642,"date":"2016-01-26T21:46:04","date_gmt":"2016-01-26T21:46:04","guid":{"rendered":"https:\/\/lpfch.org\/daniels-story\/"},"modified":"2024-01-31T23:36:34","modified_gmt":"2024-01-31T23:36:34","slug":"daniels-story","status":"publish","type":"post","link":"https:\/\/lpfch.org\/ja\/impact-stories\/daniels-story\/","title":{"rendered":"\u300c\u3053\u308c\u306f\u6642\u9650\u7206\u5f3e\u3067\u3059\u3002\u3044\u3064\u4f55\u6642\u3001\u4e8b\u614b\u304c\u60aa\u5316\u3059\u308b\u304b\u308f\u304b\u3089\u306a\u3044\u3068\u3044\u3046\u899a\u609f\u3067\u3001\u79c1\u305f\u3061\u306f\u65e5\u3005\u306e\u751f\u6d3b\u3092\u9001\u3089\u306a\u3051\u308c\u3070\u306a\u308a\u307e\u305b\u3093\u3002\u300d"},"content":{"rendered":"<h2>\u30ab\u30ea\u30d5\u30a9\u30eb\u30cb\u30a2\u5dde\u30aa\u30f3\u30bf\u30ea\u30aa\u51fa\u8eab\u306e\u30c0\u30cb\u30a8\u30eb\u3092\u7d39\u4ecb\u3057\u307e\u3059\u3002<\/h2>\n<p>\u30c0\u30cb\u30a8\u30eb\u306f\u795e\u7d4c\u7dda\u7dad\u816b\u75c7\u3092\u60a3\u3063\u3066\u751f\u304d\u3066\u3044\u307e\u3059\u3002<\/p>\n<p><img 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We have to live our daily lives knowing that things could go haywire at any time.&quot; - Lucile Packard Foundation for Children&#039;s Health<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"http:\/\/lpfch.org\/ja\/impact-stories\/daniels-story\/\" \/>\n<meta property=\"og:locale\" content=\"ja_JP\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"&quot;It\u2019s a ticking time bomb. We have to live our daily lives knowing that things could go haywire at any time.&quot;\" \/>\n<meta property=\"og:description\" content=\"Meet Daniel from Ontario, CA. Daniel lives with neurofibromatosis. 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