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- 注册时间
- 2011-9-27
- 最后登录
- 2022-11-15
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Hi. Everyone:
I am new here. I am a Chinese in USA. I am a chronicle HBVer, I just started to take tenofovir a month ago. I am working for a US Pharm company (not Gilead though). I support all the efforts for producing tenoforvir in China. Even though I am working in a Pharm company, I still believe that the profit a Pharm company make is ridiculously high. Plus that even in US, not everyone could afford to treat their illness because of the economic reason.
We, chronical HBVers, are so unfortunate. Not like people with HIVs (they get the free treatment), those HIVers may follow unhealthy live habits. Most of HBVers were either got the disease from birth, or from medical treatment (when getting injection from hospital with a unsterilized needle). I also believe that we should raise our voice to Chinese politicians, like premier WenJiaBao, It is disgusting to watch his crying all the time on TV, if he is so prone to cry, is it possible to present the real difficulties we face to him when he has a public appearance?
Below is the cost of tenofovir in US:
870$/30 tablets without insurance
35$/30 tablets with insurance.
By the way, everyone has different insurance. My insurance is 1794$/year.
Thanks.
Dan
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