tag:blogger.com,1999:blog-3753922795485552054.post294112941703706431..comments2024-03-12T05:07:19.082-07:00Comments on Not so bright & Shiny: SilenceSarahhttp://www.blogger.com/profile/07744754011059856264noreply@blogger.comBlogger6125tag:blogger.com,1999:blog-3753922795485552054.post-51493418397542544822010-08-10T18:12:20.606-07:002010-08-10T18:12:20.606-07:00I hate that you had to go through that. I hate thi...I hate that you had to go through that. I hate thinking about any parent that has to do that. I wish that 'easy' button was real.Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-3753922795485552054.post-63208741420459735332010-08-10T15:34:34.177-07:002010-08-10T15:34:34.177-07:00tears, thats all that comes to me when I read your...tears, thats all that comes to me when I read your post. I don't even know you or your children, but I feel for you and would like to help with the cause.Evan's projecthttps://www.blogger.com/profile/11586481378559400046noreply@blogger.comtag:blogger.com,1999:blog-3753922795485552054.post-64779095646619956772010-08-09T08:58:22.087-07:002010-08-09T08:58:22.087-07:00You brought something to light for me: I never put...You brought something to light for me: I never put together that those with "mild cf" can still catch the same bugs and die - for so long I said I had "mild" cf but then it got "severe" but really it's still mild, I just have severe infection that has reduced my lung function. I'm anxious about Beth and Skye, too. I hate not being near them and their families. I feel helpless to do anything but pray.Justinehttps://www.blogger.com/profile/08903730117923788153noreply@blogger.comtag:blogger.com,1999:blog-3753922795485552054.post-48780968726315687882010-08-08T22:29:36.744-07:002010-08-08T22:29:36.744-07:00I love your blog. . .as hard as it is to read abou...I love your blog. . .as hard as it is to read about the pain you're suffering right now, I love that it is so real. <br />You're absolutely right. CF took my life away from me in a matter of months as well. It fools us by making us think we will beat it, but the game is rigged for us to lose. I think your honesty about your life and your son's fight has touched many and helps people who don't live with CF understand it a little better. <br /><br />Thank You for sharing your life with us.Jamiehttps://www.blogger.com/profile/16443223033562968398noreply@blogger.comtag:blogger.com,1999:blog-3753922795485552054.post-35793346624103962922010-08-08T20:40:04.416-07:002010-08-08T20:40:04.416-07:00:(
i hate the issues.
i really do.
and i hate all...:(<br />i hate the issues.<br />i really do.<br /><br />and i hate all of this all together. i am horrible when people say be positive...because really? really? how? nothing seems to be going right anymore. and its only get worse. <br /><br />i cant imagine how you feel, so im not going to start talking like i do. but i can imagine at the same time? does that make sense?<br />i feel like i am loosing her everyday without even loosing her? <br />who know.<br /><br />im ranting. ill talk to you soon enough. <br /><br />love<br /><br />p.s. our county fair starts on the 11th, all yall are going to that here ;)Anonymoushttps://www.blogger.com/profile/08931297334966057218noreply@blogger.comtag:blogger.com,1999:blog-3753922795485552054.post-71277847541536432852010-08-08T19:24:32.729-07:002010-08-08T19:24:32.729-07:00I know, Sarah... I used to think I was a "mi...I know, Sarah... I used to think I was a "mild" CFer, then I recently caught a bug and now I'm beginning a one year course of 3 stong abx to see if it's possible to get rid of it. It's such a helpless feeling, knowing that this CF is taking my lung function. Like it must have been helpless watching it take your son. I'm sending out a huge "I Hate You" to CF for both of us. <br /><br />Much Love <3<br /><br />Stacey<br />www.confessionscyster.blogspot.comStaceyhttps://www.blogger.com/profile/08558341367213981372noreply@blogger.com