Thursday, July 23, 2009
The Daily Battles of Cystic Fibrosis
Labels:
Attitude,
CF,
Cystic Fibrosis,
Fighting,
Hope,
Hospital Stays
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Comments by IntenseDebate
7 people had something to say...:
Once again your right! It is a battle everyday and i know that i have kept up with my meds, ate everything in sight and still ended up in the hospital, as well as gotten the best pft result without doing a thing!
p.s. I watch all your videos through and through! lol
I watched the WHOLE video and thanks so much. If it's okay, I'll repost on my site and reference your site as my post tonight...? Might be going in to the joint myself tonight (hospital) if my resting O2 doesn't get more decent :( It is really really low! Gr....
Thanks much for the video!!
NOOOO. I wasn't saying you were long winded!!! Not at all!!! I'm just scared of what will be on the video. I don't want to see anything upsetting!!! I'm sorry, didn't mean to make you think you had to cut them short. This is your blog, talk away!!
Thank you! This was the exact encouragement I needed today.
Thanks again for an awesome video!!
It took me awhile to understand even if M or myself or the both of us do everything by the books its not always gonna mean he is healthy. I would get so upset and say "but we did all the treatments or but I keep the house really clean" And finally one day Dr. S looked up and me and started laughing...(I really was not seeing ANYTHING funny) And he goes "Kellee I am so sorry I have not popped your bubble sooner." And Im sure you know but the CF doctor is much more like a friend rather than a doctor so he grabs my hand and goes on with this bubble popping "Even if you pour bleach in Michaels lungs he is still going to have infection" of course he followed with "it wouldnt last long because you would kill him" but point taken so I really just now 7 years into this learning about the stuff you cant control.
Anyway sorry for the novel!!
Feel good!
You are a great motivational speaker. Thanks for you continued encouragement. I have only been following your blog for a short time now, but I look forward to it each day.
Dear Ronnie,,
I have learned more watching your video's,,, than I have at any CF appt....To me you can talk as long as you want....Thankyou for posting your PFT'S ...
Here's one or two examples of what I've learned watching you,,,,just knowing that today you said you don't feel good after 8 days in the hospital...My little one always looks like she's at death's door in the hospital,,literally, eyes will be blue/black,, throwing up buckets of blood,,very restless,, the raspy voice,, heart pounding so fast,, sats drop,,etc, you know what I mean...She just turned 8, but looks like she's 5 (she's so tiny),,but don't dare tell her she looks so tiny(she hates when people say that to her).
I used to think,my God, do they know what thier doing??? Why isn't she getting better??? She looked better before she came in...
I guess I'm trying to say,, It helps to see what another CFer is going through when they are in the hospital...
I'm very sorry your not feeling well today ,,,,and you do give me alot of hope and encouragement..
I pray you start to feel better quickly.God Bless You,,Karla
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