Lymphoma since 11/2015 ~ 8次化療 + 15次電療 ******************************** My new blog & youtube channel ~ vmacook*vmawet
關於我自己
- vvma Vs Lymphoma
- 我寫這個BLOG希望給關心我的人知道我每天的近況,亦希望如有同樣遭遇的人, 應同我一樣積極面對,我的努力是愛我的人給我支持,我的回饋就是盡全力面對,戰勝癌症。 I created this blog because I want to let those who cares about me know what I am doing and feeling. And I hope those people like me would live happily and being positive. I have a strong backup by all my loved and what I can do for them is to fight cancer. 歡迎大家留言,比個支持我呀! Welcome to leave comments and support. Thank you.
2016年1月20日 星期三
第二至四晚威爾斯 The 2nd - 4th Night
第一晚已不好過, 要抽住藥架, 又要抆電製, 又要插電製, 個廁所感應器又過敏, 未坐低已沖水。瞓得好差。
但旁邊的印印, 即使姑娘不準佢落床, 佢照落, 佢每次去廁所, 令我壓力加重, 又怕佢有事, 又怕佢有事時整到我。
但又有事發生, 聽到印印傷風同咳, 但每朝醫生問佢, 佢又唔講。終於有天, 佢發燒, 但醫院即時沒有調走印印。於是我忍不住同姑娘講, 佢有咳, 有痰, 有傷風。姑娘即時問佢鼻涕顏色, 我聽到話黃色, 即時心實一實, 唔係呀, 我而家咁弱, 旁邊有事仲唔轉走佢 ? 最後, 佢都留多了一晚, 直至報告證明佢有副流感,才調到獨立房。姑娘入黎仲要同我講, 你都要帶口罩保護自己, 唔係呀, 醫院唔係要安排好的嗎? 只要發燒, 都要隔離一下先啦。
今天好朋友探我, 又帶了其他朋友的書、頭巾給我。
It is not an easy night. I need to unplug the electricity supply and plug it back when I go to toilet. The sensor of the flush is really annoying as it is so sensitive.
The Indonesia room mate does not listen to the nurse. She keeps getting off her bed and that makes me worry. I don't know how to handle her if she faint again and I am worrying that if she fells, she may pulls off my stuff.
Then, something happened. She had fever. But she never tells her doctor about her running nose and cough. So I tell the nurse and she tells the nurse that her spit is yellow. I know that she is not ok. But they did not move her out under the report proved that she had flu. I am wondering why they do not move her out once she had fever. It is really dangerous that they also had to protect me.
I have a visitor today. She brings also the books and the scarf from my friends.
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