Just a few things to mention to our new friends here on HW in the CF room. As I remember things that needs attention, I will post it here for all members.
Please remember to:
1. Read your forum rules, under forum links, and keep them in mind when you are posting, to avoid moderator or admin editing.
2. Check for dates on posts, some posts may be outdated and that person may not post anymore.
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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