Guest guest Posted August 28, 2006 Report Share Posted August 28, 2006 Thank you so much . I can't wait to look at them! :-) Cyndi (DAD, IPF 12/05) wrote: Hi Cyndi I am also a research nut, so here a few site of interest. P UIP 8/00 http://www.coalitionforpf.org/AboutUs/resources.asp http://www.pulmonaryfibrosis.org/patient.pdf http://www.findarticles.com/p/articles/mi_m0984/is_6_122/ai_96306238 http://findarticles.com/p/articles/mi_m0984/is_5_128/ai_n15967367 http://www.fightipf.com/wt/page/index http://www.pilotforipf.org/patient_tools.php Peggy <pac1773cfl (DOT) rr.com> wrote: Hi Cyndi and Anne, Please help your Dad find all the sites you can on thecomputer.. As a IPFer I want to know everything. My family upsets me so muchtrying to protect me. I'm fine, my mind still works well and I do want a sayover my life even if I have to depend on them. I just simply can't breathwell. Ask him questions about how he feels about this monster and beprepared for a lot of different feelings to show. It is harder to deal withwhen your thoughts are trapped inside for fear of talking to our families.God Bless you both for helping your Dads.Much Love and Prayers, Peggy 9/04 ipf> Hi Anne,> That is exactly what my dad's doctor told us. My dad is already obsessed with> researching this disease and finding out what stage he is in. We haven't> bought one yet, but he wants one.> Cyndi (DAD IPF 12-05) . Get your own web address for just $1.99/1st yr. We'll help. Yahoo! Small Business. Quote Link to comment Share on other sites More sharing options...
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