星期一覆診, 白血球又回落至1.6, 不過不用打白血球針. 但咳已令人很辛苦, 痰卡在氣管咳唔出, 鼻涕貼緊鼻腔呻唔到, 真辛苦。雖然已於上星期六睇了馬醫生, 食完藥沒有上次的有效。終於今天威爾斯的譚醫生開了傷風敏感藥及化痰藥, 今天已比前幾日舒服了些, 希望咳快停。另外, 開始覺得手指頭有點麻及觸電感覺。
明天又要到威爾斯覆診。祈求天父快把我的咳醫好, 使我身心回復平靜。
I went back to Hospital for check up on Monday. The white blood cell count back to 1.6 but the doctor do not need me to take the filgratm Syringe. My cough made me really tired. The spit are so sticky and cannot come out. Although I visited Dr. Ma last Saturday, the medicine seemed not working at all. But Dr. Tam gave me the medicine on Monday and it worked. I feel better these few days. By the way, I feel a bit paralysis.
Tomorrow, I will go for follow up check at Prince Wales Hospital. I pray for Lord that hope He could heal my cough and make my heart peace and calm.
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.
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