Hi Everyone!
It's extremely important to "me" and to "HW" to have such a wonderful place for everyone to come to and post your thoughts, lend a shoulder, ask questions, etc.
I volunteer my time as a moderator here on HW in the CF Room and would like some help, of course with the already confirmed approval from the Admin. 
If you would like to volunteer your time as a co-mod, please send your interested email to me. To: Womanoftx@aol.com.
I'm not really looking for anyone per say in particular, but, would like to know of your experience with CF, why you would be a good candidate for co-mod and have you been a prior moderator on a forum, etc. I will then get another approval from the Admin after the selection is made and post on the forum who the new co-mod will be.
Did I tell everyone.....I enjoy being a part of HW! and hope you do too!.
Hugs!
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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