■冰桶挑戰，救漸凍人■
ALS，肌萎縮性脊髓側索硬化症
大家好，我是台灣的COSER KING ♥(✿ฺ´∀`✿ฺ)ﾉ
來自香港的M仔與英國的ALEX
你們的指名挑戰我看到了
我想，不是你們的指定挑戰，
我是一輩子都無法走出這個陰影。o´ﾟ□ﾟ`o
四年前，我的死黨，最好的兄弟，
再被醫生告知罹患ALS後，(ΘˍΘ=)
他從一個健康熱愛運動的男人，
到無法再跟我一起打球，
無法行走，無法寫字，無法說話，
而一年後，他過世了。 ˚‧º•(˚ ˃̣̣̥᷄⌓˂̣̣̥᷅ )‧º•˚
我一直認為，這一輩子，
ALS這個無藥可解的疾病，
將會是我心中的永遠無法去正視的問題。(ू ˃̣̣̣̣̣̣o˂̣̣̣̣̣̣ ू)
現在，再查過很多資料後，
我想我該是正視這個問題與疾病，
每位病患，除了需要醫生的治療外，
更需要志工與社會上的幫助。 o(･∀･)o
我不再指定任何朋友，願意宣導這項捐款活動的朋友，
也希望你們可以跟我分享你的影片，
讓更多知道這個所謂的罕見疾病ALS，
一起用影片與捐款行動去支持他們。 +.(*’v`*)+
請上網搜尋"ALS" d(‘v`●)
讓我們用小額捐款與影片宣傳一起幫助他們
加油!!!!!!!!!
Amyotrophic lateral sclerosis (ALS) Greetings for everyone, it’s Taiwanese coser KING.
I have well received the tag from my Hong Kong friend, Yakko and Alex from the UK.
Without your tags, I bet I would never walk out from my gloomy past. It was 4 years ago my best bro was certified of having ALS.
He used to be a Sports holic yet he could no longer play ball games with me, walk, write or even speak. He passed away one year after.
I believe, in my limited life being, ALS will remain cureless and the pain that I could never face. But after a lot of research,
I think I have to start look into this matter. Apart from doctors, more volunteers and social support will be required for the patients.
I will therefore not tagging anyone, WHOEVER would like to promote this ice bucket donation event could share your videos with me and let more people aware of this rare disease. Please kindly show your support by videos and donations.
You may start with googling “ALS” online, donating small amount of share and promoting your own ice bucket videos. Let’s go for it and wish for all the best!
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