FOR FAMILIES
失語症患者家屬
In Aphasia HK, we aim to provide a platform to connect with families suffering from similar situations.
我們希望在香港為病患者的家屬提供實際以及身心靈上的支援。當中包括:
Supporting groups for Wives
患者妻子支援小組
We provide regular meet-up for wives having husband suffering from Aphasia. Chinese women has strong domestic strength in taking care of husband daily living, yet a comfortable platform for emotional support and encouragement are necessary for healthy mankind.
我們為失語症患者的妻子提供定期見面約會。在中國人的家庭觀，妻子多是以家務及照顧為中心，小組多以情緒支援及社區聯繫為重心，讓妻子們面對溝通困難時能有其他社區會員協助。
Supporting group for Husband
患者丈夫支援小組
We provide regular meet-up for husband having wives suffering from Aphasia. Chinese husband tends to be introvert when encountering family crisis. They may be, or maybe not, understand the changes brought by irreversible diseases like Aphasia. Husband, too, has to adopt to a new way of communication in a life-long courtship.
我們為失語症患者的丈夫提供定期見面約會。丈夫多多年來以工作為先養家為主，對於家庭的改變，偏向比較保守及內斂。在未能與妻子溝通時也欠缺尋求協助的主動性。小組為男士們提供實用的資訊，讓他們能適應家庭中新的溝通模式以及夫妻關係。
Support group for children and grandchildren
患者子女及孫兒支援小組
Majority of Patient suffering from Aphasia reached retirement age. Their children has been in school or even become independent young adult. Some may not fully understand the long term adjustment their parents have to make due to Aphasia.
大部份還有失語症的病者都年屆退休年齡。當中很多子女已經成家立室獨立生活，有些甚至兒孫滿堂。要接受溝通上的改變為下一代不是簡單容易的事。支援小組希望提供定期聚會，或工作坊，直接把溝通技巧分享。讓下一代也明白如何與失語症的患者好好溝通
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