[寶寶] 來自罕病治療醫師的沉痛呼籲
純轉貼,原文來自
https://www.facebook.com/nancy.chien.98/posts/1466754833338801
今天的門診來了一對夫妻,帶了一個滿3個月的寶寶,要求補做新生兒篩檢.
通常這種夫妻會來補做的原因,最多是因為美寶,以為人家沒幫他們美寶做(其實台灣最
多人去的加州是有做的,跟台灣只差一項疾病);再不然就是因為五個月大了要打疫苗,
被對方要求要出示安全證明但是拿不出來.今天來的不是.純粹是因為“國泰(其他家也
有過)”保險業務員說:要保單成立後再做篩檢.
我知道google大神手下的保險業務說,衛福部有補助的項目還是做吧,自費的不要做就好
(google大神知道衛福部有補助的項目還是算自費的嗎?)但是今天這個,是連有補助的
項目都還沒做!!!!
他現在已經3個月又幾天大了.爸媽用盡心血,為了要這個商業保險,保證寶寶未來有醫
療需求可以使用(或是儲蓄險etc),讓保險業務賺了業績,讓保險公司賺飽飽“應該是篩
檢正常沒問題”個案的保費(而篩檢異常個案應該要出險的部分都免付),但是,寶寶如
果真有這些原本可以藉由篩檢及早治療的問題,因為要投保而延遲診斷或治療,導致寶寶
救不起來,或是救起來也是嚴重智力受損,誰擔這個後果?
我們偉大的健保讓寶寶一出生就可以依附在媽媽的健保檔內(只要不是美寶,台寶是即使
媽媽沒健保身份還可以用爸爸的健保檔),用媽媽(或是爸爸)的健保卡,不就是為了提
供寶寶一出生就有無縫接軌的保障嗎?
我警告家長去金管會告國泰那個業務員.心裡想著,阿彌陀佛菩薩上帝阿拉保佑,看來這
個寶寶沒事.
其實這幾年,這種拒檢的個案越來越多,身為罕病治療的醫師兼篩檢中心負責人,我已經
聽說了好幾個拒絕了被篩檢的機會的寶寶,等到知道時都已經太遲了.
爸媽們:你們知道你們究竟做了什麼事嗎?
----
補心得: 新手爸媽之前在板上爬文也曾看到不少推文建議先保險再做部分檢查
雖然 FB 內的醫師沒有指明是那些罕見疾病,不過如龐貝氏症的話,
確實不該等保險保完才做檢查,因為龐貝氏症越早開始做治療越好
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※ 編輯: paulyanzi (1.171.56.29), 11/01/2016 18:17:51
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