Cystic Fibrosis Forum (EXP)

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Recent content by Kyrav

  1. K

    Simple question for cf'ers who are under 30% FEV1 (or post-transplant) see inside

    I've been right around 30% for almost a year and a half.
  2. K

    What else could go wrong

    Thank you all for your insight and words of encouragement. I am by no means about to let one more thing bring me down, like I said in my original post I was just irritated that there always seems to be one more thing. As for the surgeries, I cannot have the acid reflux surgery before transplant...
  3. K

    What else could go wrong

    Hello my fellow cfers. Im just going to jump right in, I'm 25 and I just finished my evaluation for transplant and found out I will be getting listed for both lung and liver. However, when I got a ct scan of my abdomen they saw some of the nodules on my liver do something called "washing out"...
  4. K

    what to do when i get frustrated/sad/discouraged

    I agree with nocode. I thought I would be so bored when I had to quit my jobs, but when I got to this point doing all my treatments has become my job. As for doing stuff with friends, I go out when I have the energy. Usually just to lunch or a movie or something. Sometimes they just come over to...
  5. K

    Cayston in the Hospital

    I get taken off my inhaled TOBI and Cayston while I'm in the hospital. I asked my NP about it once and she said they are fighting the same thing, so when you're on iv TOBI it would kinda be like doubling up.
  6. K

    So frustrated about telling my non cf friends about cf

    My mom comes with me to every transplant dr appointment/meeting, I think it's important because she's going to be my primary caregiver afterwards so having her know as much as possible I think is a great thing. My dad comes to the classes and meetings but not necessarily all the procedures. My...
  7. K

    Hemoptysis

    I hate to say it, but I'm relieved this has happened to other people. It makes me feel better to hear its not totally uncommon. As for fixing it, when I was in the icu they said if it continued to happen they would do the whole embolizing thing. And I was put on 15mg of vitamin K the reminder...
  8. K

    Hemoptysis

    I've been on pulmozyme as long as I can remember. They did have me on the 7% hypertonic saline when i first went in, at home I only do 3%. But after I had my little episode they stopped both for a couple days. Has it continued to happen to you even though you've stopped the pulmozyme? What...
  9. K

    Hemoptysis

    Hi everyone. I just got out of the hospital a couple days ago but while I was in, a few days after I had been admitted, I coughed up blood. And it wasn't just a little, they said it was probably about 200cc which i believe is almost a cup of just blood, no sputum. I was put into the icu for the...
  10. K

    3 months Post Transplant...

    I love hearing about people doing so well after surgery! It gives me hope for when I have my own. Hope you all stay healthy and happy!
  11. K

    How did your decline go?

    I was actually really surprised at how fast it happened to me, I had never really heard of anyone all of a sudden just getting way worse so I think it's a fair question to ask. In march last year my baseline was in the mid 50's and I was not on oxygen. In April I had a really bad exacerbation...
  12. K

    CF and Sleep Meds

    I was prescribed trazadone for sleep by my cf clinic. My sleeplessness is usually due to stress and my mind going a million miles an hour.
  13. K

    24 hour ph study

    Update: I was able to get through the 24 hours. Being inpatient was what made it so much easier. I got Adavan to help keep me relaxed the whole time it was in, and it also helped keep me close to sleeping the majority of the time as well. I was also given benzocaine (a numbing spray) to numb my...
  14. K

    24 hour ph study

    Hi everyone. As of right now I only need one more test before my lung and liver team present my case to the transplant committee. It's the ph study, you know, the one where they shove a tube up your nose and down your throat to measure your acid reflux. Anyway, I tried it outpatient last week...
  15. K

    Exercising???

    Hey, I'm in eval for transplant as well and have been doing a pulmonary rehab program to keep my strength up. I find it does take a lot out of me too. I do the treadmill and resistance bands, taking breaks from the bands every other day. I've found that even just that hour three or four times a...
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