tag:blogger.com,1999:blog-6932055770954013719.post3238527504119066602..comments2023-09-27T10:03:43.618-05:00Comments on Fighting Cystic Fibrosis One Day at a Time: FrustrationsCourtniehttp://www.blogger.com/profile/05032154054139102775noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-6932055770954013719.post-87233226532198498632009-07-02T22:58:43.728-05:002009-07-02T22:58:43.728-05:00we have the same problem, i just don't listen ...we have the same problem, i just don't listen to him lol i only change something if his CF doc says so. i feel your pain!tammyhttps://www.blogger.com/profile/04186200621327476751noreply@blogger.comtag:blogger.com,1999:blog-6932055770954013719.post-8547551601707348582009-03-02T14:46:00.000-06:002009-03-02T14:46:00.000-06:00Tricia says it's cool to use her poem.Tricia says it's cool to use her poem.CFHusbandhttps://www.blogger.com/profile/15834715315798433983noreply@blogger.comtag:blogger.com,1999:blog-6932055770954013719.post-84627792123209224962009-03-02T11:42:00.000-06:002009-03-02T11:42:00.000-06:00we are really, really lucky that our cf dr. lets u...we are really, really lucky that our cf dr. lets us abuse him. we use him as our pediatrician. the only time we go to the real ped is when it is something SO totally unrelated (wart removal, tetanus shot, etc). <BR/><BR/>hope everything is okay with mr. luke's liver. keep us posted!Debhttps://www.blogger.com/profile/07896271627723253157noreply@blogger.com