Cystic Fibrosis Forum (EXP)

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  1. C

    Great Strides!

    Hello all! Been a while since I posted here but I just now got internet once again. BUT! I will be participating in my first ever Great Strides walk this year. I'm super stoked! Could anyone tell me what it's like? I know it depends on location, but are there usually good turn outs? And...
  2. C

    Great Strides!

    Hello all! Been a while since I posted here but I just now got internet once again. BUT! I will be participating in my first ever Great Strides walk this year. I'm super stoked! Could anyone tell me what it's like? I know it depends on location, but are there usually good turn outs? And...
  3. C

    Great Strides!

    Hello all! Been a while since I posted here but I just now got internet once again. BUT! I will be participating in my first ever Great Strides walk this year. I'm super stoked! Could anyone tell me what it's like? I know it depends on location, but are there usually good turn outs? And...
  4. C

    I've got the magic in me!

    Anyone else got that **** song stuck in their heads? I KNOW I DO!
  5. C

    I've got the magic in me!

    Anyone else got that **** song stuck in their heads? I KNOW I DO!
  6. C

    I've got the magic in me!

    Anyone else got that **** song stuck in their heads? I KNOW I DO!
  7. C

    Facebook?

    Sorry if a thread already exists of this. I'm viewing the forum from my cell phone and it won't let me search. But I love talking and being in contact with other CF'ers. Whether it be for general convo about non CF related stuff or for a support system. So, if you have a facebook, add me...
  8. C

    Facebook?

    Sorry if a thread already exists of this. I'm viewing the forum from my cell phone and it won't let me search. But I love talking and being in contact with other CF'ers. Whether it be for general convo about non CF related stuff or for a support system. So, if you have a facebook, add me...
  9. C

    Facebook?

    Sorry if a thread already exists of this. I'm viewing the forum from my cell phone and it won't let me search. But I love talking and being in contact with other CF'ers. Whether it be for general convo about non CF related stuff or for a support system. So, if you have a facebook, add me...
  10. C

    My new CF Tattoo!

    They still drop. They'll go down to about 60% when I'm sick..but they usually never stay there.
  11. C

    My new CF Tattoo!

    They still drop. They'll go down to about 60% when I'm sick..but they usually never stay there.
  12. C

    My new CF Tattoo!

    They still drop. They'll go down to about 60% when I'm sick..but they usually never stay there.
  13. C

    Tobramycin bad breath????

    I go on inhaled Tobi every other month to keep infection down and yea, it'll give you pretty bad medicine breath. Also via IV too. It also destroys my throat via neb...kinda like inhaling razors, lol. And it could also be infection because anytime I cough a lot and work up some of the mucus...
  14. C

    Tobramycin bad breath????

    I go on inhaled Tobi every other month to keep infection down and yea, it'll give you pretty bad medicine breath. Also via IV too. It also destroys my throat via neb...kinda like inhaling razors, lol. And it could also be infection because anytime I cough a lot and work up some of the mucus...
  15. C

    Tobramycin bad breath????

    I go on inhaled Tobi every other month to keep infection down and yea, it'll give you pretty bad medicine breath. Also via IV too. It also destroys my throat via neb...kinda like inhaling razors, lol. And it could also be infection because anytime I cough a lot and work up some of the mucus...
  16. C

    My new CF Tattoo!

    Yea. My Mom kinda beat it into my brain to do my Therapy so it's kinda stuck with me throughout the years. I'll get slack occasionally...like right now I haven't done my vest in about 4 days. But I make up for it with exercise and I'll do it like, 6 times a day if needed, haha,
  17. C

    My new CF Tattoo!

    Yea. My Mom kinda beat it into my brain to do my Therapy so it's kinda stuck with me throughout the years. I'll get slack occasionally...like right now I haven't done my vest in about 4 days. But I make up for it with exercise and I'll do it like, 6 times a day if needed, haha,
  18. C

    My new CF Tattoo!

    Yea. My Mom kinda beat it into my brain to do my Therapy so it's kinda stuck with me throughout the years. I'll get slack occasionally...like right now I haven't done my vest in about 4 days. But I make up for it with exercise and I'll do it like, 6 times a day if needed, haha,
  19. C

    Who are you in a nut shell

    who are you Well, the name's Morgan. I'm a guy. Yea, I have a chicks name. I'm 20. 21 on July 8th! Diagnosed at 3 months old. DeltaF508 FTW! I keep my FEV's between 89-93%. No one else in my Family on either side has CF. Lucky me, right? I've had about 10 sinus surgeries when I was younger...
  20. C

    My new CF Tattoo!

    What's up everyone? It's been a while since I've been on here. SO long that I had to make a new account, lol. But I figured I would share my new CF Tattoo I got about a week ago. I got a broken hour glass with the CF ribbon wrapped around it in traditional flash art style on my right hand so...
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