cf

hi my name is frank and i'm 36 yrs old with cf. am new to computers and obviously forums too. this is really very interesting to me since i've never had a place likethis to share concerns with other cf patients. so far i've have never been hospitalized in my life and am healthy. don't know why i'm lucky and even sometimes feel guilty that others suffer with more severe cases. but i do have many questions and concerns  that i'd like to share with other cf patients. and of course will try to answer any questions others might have for me. i'm sooo happy to have found something like this. will respond to all friends. thank you so much.  one of my first questions of interest was my lack of smell. i know many cf patients have polyps (as do i) but i have never ever been able to smell since infancy. so polyps probably not the cause. does anyone know of this in any other cf patients?? hope to talk to many of you soon bye and thank you

Hi Frank, Welcome to HW!.

Awsome News on staying healthy! We are a friendly group here on HW. If you care to see who all is a part of the CF Room, step on over, add your info and check out others as well. Go to thread...Sound Off: CF Member Room.

Again, welcome and enjoy your stay!
Hugs!

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Kathy, mom to identical twin boys with CF (10 yrs), daughter 21, grandaughter 3, Newborn grandson

 
If there is a CURE for Cystic Fibrosis this very moment and this is "not soon enough"...you would hear this twins mom "Across America" "YESSSSSSSSSS"!!.

Moderator, Cystic Fibrosis.  "If there is questionable doubt, check it out"....with your healthcare provider!.  We are here to offer support, encouragement, a shoulder to lean on, and answer your questions as best we can.  Don't hesitate to step on in and enjoy and remember!  "Never give up hope for a cure" one day we will get there!".  

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