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再见了妈妈。女儿将您剩下的药物在此捐赠,希望您走后还能继续帮助活在这个世界上的

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发表于 2008-6-16 08:24:13 | 显示全部楼层 |阅读模式 来自: 中国安徽合肥
<p><font face="楷体_GB2312" size="4"><strong>妈妈非小细胞肺癌,腺鳞结合,06.6发现时3期. 到现在化疗过两次(都半途而废,因为反应太大,而且后来检查效果几乎没有,肿瘤还在化疗期间长大),放疗四五次,吃光量已经超了. 07.4-08.4吃易瑞莎,耐药后肿瘤又明显发展,再吃特罗凯,至今一个多月未有明显效果(皮疹腹泄也只有一点,但持续存在). </strong></font></p>
<p><font face="楷体_GB2312" size="4"><strong>吃易和吃特,都是肿瘤科主任给的方子,但看了大家的易耐药方案,不知道为什么医生没给力比泰方案,我家是合肥,难道合肥最大的医院没有这个药吗?</strong></font></p>
<p><font face="楷体_GB2312" size="4"><strong>现在妈妈身体一天比一天虚弱,走路已经摇摇晃晃,偶尔会咳嗽得喘不上气,睡觉时平躺会胸闷,呛咳,侧躺会胸疼.一定要改治疗方法了,不能这样拖下去. 可是现在是应该想办法上力比泰的方案还是到北京找黄金昶,或者哈尔滨的张宗歧呢?</strong></font></p>
<p><strong><font face="楷体_GB2312" size="4">现在要妈妈出门是件大事,一定要安排好所有的东西,保证是比较好的去向,才能让她动.而且,每给她一次希望,再失败,都会让她更加绝望.妈妈很坚强,这两年一直很坚强,可是在易耐药后这一两个月,明显一天比一天差,她也开始情绪不好了...</font></strong></p>
<p><strong><font face="楷体_GB2312" size="4">大家有意见的给点意见吧!</font></strong></p>
<p><strong><font face="楷体_GB2312" size="4">更新见跟贴.谢谢大家帮助!</font></strong></p><br/><br/>
<p><font face="Verdana">2008.8.20</font></p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp; 2008年8月15日晨,母亲终因呼吸困难逝世.享年57岁. </font></p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp; 感谢这半年多来坛里各位的帮助和关心.将剩下的药物捐赠.</font></p>
<p><font face="Verdana"></font>&nbsp;</p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp; 英版易瑞沙14粒. (吃6个月有效后获赠的药)</font></p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp; 瑞士罗氏 特罗凯 12粒.&nbsp; (安徽医科大学第一附属医院购的药)</font></p>
<p><font face="Verdana">&nbsp;&nbsp; </font></p>
<p>&nbsp;&nbsp;&nbsp; </p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp; 因为都是正版药物,很贵的药,最好是想试用的病友来申请,一般3-5粒病人即可感觉到是否有效.</font></p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp; 也请得到我母亲帮助的朋友,为我的母亲祈祷祝福.</font></p>
<p><font face="Verdana"></font>&nbsp;</p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp; 需要的朋友加我QQ24119043 这几天我会隐身在线.</font></p>
<p><font face="Verdana"></font>&nbsp;</p>
<p><font face="Verdana">S:对于申请的人,也许我会问许多问题,希望您能认真配合,因为不想这么昂贵的药物落到不该得到的人手里。</font></p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 最好是合肥的病友,可以当面了解。</font></p>
<p><font face="Verdana">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 药贩请自重!</p>
<p><br/>8.22</p>
<p>&nbsp;</p>
<p>&nbsp;&nbsp;&nbsp;&nbsp; 易瑞沙14粒已经分两次捐完.一位深圳病友,一位西安病友,深圳的已于8.22下午快递邮出,西安的准备明天8.23快递邮出. 因为是QQ联系,不知道在论坛的名字,请跟贴证明.谢谢!</p></font>
[此贴子已经被作者于2008-8-22 19:01:18编辑过]
有爱,就有奇迹!
发表于 2008-6-25 13:04:48 | 显示全部楼层 来自: 中国天津
<p><font color="#119911"><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">杏仁露,你妈妈和我妈妈的情况很像啊,我妈妈也是确诊时化疗两次,方案是多西他赛</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">+</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">卡铂,两次的副作用都很大,恶心呕吐,白细胞</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">1900</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">,肺感染,第一次评价只是稳定,第二次化疗后,病情就进展了,双肺弥漫小结节,磨皮玻璃样变,一活动和说话就气喘,几乎</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">24</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">小时吸氧,没办法只能试试易瑞沙了,从</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">2007</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">年</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">11</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">月</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">7</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">日开始服用,有效,但是我妈妈没有你妈妈这么幸运,才吃了六个多月时就耐药了,我一点思想准备都没有啊,医生说易的耐药期因人而异的有</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">3</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">个月到</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">3</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">年不等,没有办法耐药了也要面对。我这些天也是在为下一步的方案奔走啊,我很理解你现在的心情,我也是不敢再给妈妈做化疗了,有上次化疗的经历,我很担心这次化疗也像上次一样,不能耐受副作用不说,反倒加速了病情的发展,我也想直接换特罗凯,可是看到这么多病友,易耐药后换特基本上都无效,我也没信心了,现在是进退两难啊!从</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">6</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">月</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">3</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">日复查</span><span lang="EN-US" style="FONT-SIZE: 14pt; FONT-FAMILY: &quot;Times New Roman&quot;; mso-bidi-font-size: 12.0pt; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA; mso-fareast-font-family: 宋体;">CT</span><span style="FONT-SIZE: 14pt; FONT-FAMILY: 宋体; mso-bidi-font-size: 12.0pt; mso-ascii-font-family: &quot;Times New Roman&quot;; mso-hansi-font-family: &quot;Times New Roman&quot;; mso-bidi-font-family: &quot;Times New Roman&quot;; mso-font-kerning: 1.0pt; mso-ansi-language: EN-US; mso-fareast-language: ZH-CN; mso-bidi-language: AR-SA;">显示耐药到现在肺部的症状还不是太明显,所以我还是让我妈继续吃易,皮疹还是有的。还有就是胸科的主任也提到阿瓦斯丁了,好像我们这也不好买的,还有就是费用,听说贵的惊人,我家是工薪阶层,哎!我们要多沟通啊,有什么问题和经验多交流。祝好!</span></font></p>
有爱,就有奇迹!
发表于 2008-6-16 08:46:01 | 显示全部楼层 来自: 中国山东菏泽
<p>病人身体虚弱,经不起折腾的,又何况,我们折腾来折腾去又能给病人减少多少痛苦呢?</p><p>我爸爸也面临无路可走的状态,我打内心里不愿让他去医院了,化疗太冒险,住院对他造成的心里压力也会很大,特别是在隐瞒病情的情况下。得不偿失。</p><p>不去医院又怕爸爸伤心,他会不会感觉儿女们把他抛弃不管了,那样岂不更痛心。</p><p>我现在很重视病人的精神和饭食,想方设法保证好这两样。其余再尝试点无毒的偏方,比如吃壁虎粉。走投无路了。。。。</p>
有爱,就有奇迹!
 楼主| 发表于 2008-6-16 08:54:55 | 显示全部楼层 来自: 中国安徽合肥

[求助]这样的情况,下步怎么走?帮帮我吧,帮帮我吧,妈妈需要希望!

<font face="楷体_GB2312" size="4"><strong>唉,还好,我妈妈是从开始就知道病情的(知道大多数). 确实,也不敢轻易谈化疗了,上两次化疗的失败,对妈妈不仅在身体上造成了巨大的伤害,更是在心理上粉碎了对化疗的希望,所以对力比泰方案,一直不敢提...可是这样姑息,只是吃特罗凯以赚取心理安慰,是不行的啊!怎么办怎么办!!</strong></font>
有爱,就有奇迹!
发表于 2008-6-16 10:46:45 | 显示全部楼层 来自: 中国北京
<p><font size="4">唉,我知道此时说再多安慰的话都显得很无力。我妈妈服易也耐药了,我现在和你面临同样的困惑!</font></p><p><font size="4">和奚琴的观点一样,我不建议你再带妈妈四处求医!癌症的治疗,全世界无非都那几种方法,放化疗、X刀、伽玛刀、靶向、中医。。。。。。合肥是省会城市,力比泰肯定会有,如果打算用,建议你再多询问三甲医院。</font></p><p><font size="4">看你的描述,你妈妈的体力已经有些虚弱了,再四处奔波,反而不得休息会更吃不消。至于你提到的张宗歧,是北京的中医大夫。我上周刚带妈妈去问过诊,领取了一些中医。是北京普祥中医肿瘤医院的。因为妈妈刚刚服用,效果还不清楚。我们也是病急乱投医!多给妈妈些精神鼓励,如果能够中西医结合,或许会带来些好效果!</font></p><p><font size="4">祝福我们的亲人!</font></p>
有爱,就有奇迹!
发表于 2008-6-16 11:36:37 | 显示全部楼层 来自: 中国广东深圳
说实话,省立真的不怎么样,我妈妈是4期,在省立做了三次化疗,现在身体很差,最后主治医师居然调走了。开始考虑易瑞沙了,买不起英版,又找不到印版途径,真是有点绝望。[em10]
有爱,就有奇迹!
 楼主| 发表于 2008-6-16 14:36:28 | 显示全部楼层 来自: 中国安徽合肥

[求助]这样的情况,下步怎么走?帮帮我吧,帮帮我吧,妈妈需要希望!

<p><font face="楷体_GB2312" size="4"><strong>这么多同病中人啊</strong></font></p><p><font face="楷体_GB2312" size="4"><strong>妈妈是在安医看的,不是省立. 让人郁闷的是,放疗主任开放疗的方子,肿瘤主任开他的方子,两个都算主治医生,也都不能算. 还相互说对方的疗法不对...郁闷.</strong></font></p><p><font face="楷体_GB2312" size="4"><strong>有人知道鸭蛋籽是什么吗?上周看了省立的林主任(中医),她给提到的药,可是在网上查,却只查到治疗"瘊子""疣"什么的资料,求助!</strong></font></p>
有爱,就有奇迹!
发表于 2008-6-16 14:46:33 | 显示全部楼层 来自: 中国安徽合肥
我也是安徽合肥的,老爸肺鳞两年了,瘦弱不堪,前一阵子咳血、浮肿住院,现在决定吃特罗凯了,但愿有效!鸦胆子是中成药,据说治疗脑转有些效果。QQ:369693915
有爱,就有奇迹!
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