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Sandy: You are SOOO welcome here. You know (because I say it often) I love Matt's art~ my Chagall like friend~ Glad you're welcoming a new baby in 2008! Love, Jeanne
<a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.com/art_gallery.html">Click on Matt's Art~</a>
Sandy: You are SOOO welcome here. You know (because I say it often) I love Matt's art~ my Chagall like friend~ Glad you're welcoming a new baby in 2008! Love, Jeanne
<a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.com/art_gallery.html">Click on Matt's Art~</a>
Sandy: You are SOOO welcome here. You know (because I say it often) I love Matt's art~ my Chagall like friend~ Glad you're welcoming a new baby in 2008! Love, Jeanne
<a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.com/art_gallery.html">Click on Matt's Art~</a>
Sandy: You are SOOO welcome here. You know (because I say it often) I love Matt's art~ my Chagall like friend~ Glad you're welcoming a new baby in 2008! Love, Jeanne
<a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.com/art_gallery.html">Click on Matt's Art~</a>
Sandy: You are SOOO welcome here. You know (because I say it often) I love Matt's art~ my Chagall like friend~ Glad you're welcoming a new baby in 2008! Love, Jeanne
<a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.com/art_gallery.html">Click on Matt's Art~</a>
Oh no Victoria, Please take comfort from all of us...prayers and thoughts to Little G-Man, you and your family...a safe ride back home to Chris!
<a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?forumid=102&CFID=402530&CFTOKEN=69356182">VMHoward's...
Oh no Victoria, Please take comfort from all of us...prayers and thoughts to Little G-Man, you and your family...a safe ride back home to Chris!
<a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?forumid=102&CFID=402530&CFTOKEN=69356182">VMHoward's...
Oh no Victoria, Please take comfort from all of us...prayers and thoughts to Little G-Man, you and your family...a safe ride back home to Chris!
<a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?forumid=102&CFID=402530&CFTOKEN=69356182">VMHoward's...
Oh no Victoria, Please take comfort from all of us...prayers and thoughts to Little G-Man, you and your family...a safe ride back home to Chris!
<a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?forumid=102&CFID=402530&CFTOKEN=69356182">VMHoward's...
Oh no Victoria, Please take comfort from all of us...prayers and thoughts to Little G-Man, you and your family...a safe ride back home to Chris!
<a target=_blank class=ftalternatingbarlinklarge href="http://blogs.cysticfibrosis.com/index.cfm?forumid=102&CFID=402530&CFTOKEN=69356182">VMHoward's...
Nervous1...I know there other members who don't have CF but feel comfort here because of the similar symptoms. You are an e-patient and we welcome you.
I know from speaking with Bruce at Ambry that there are 1800 possible mutations. The list seems to be growing. Welcome back and hopefully...
Nervous1...I know there other members who don't have CF but feel comfort here because of the similar symptoms. You are an e-patient and we welcome you.
I know from speaking with Bruce at Ambry that there are 1800 possible mutations. The list seems to be growing. Welcome back and hopefully...
Nervous1...I know there other members who don't have CF but feel comfort here because of the similar symptoms. You are an e-patient and we welcome you.
I know from speaking with Bruce at Ambry that there are 1800 possible mutations. The list seems to be growing. Welcome back and hopefully...
Nervous1...I know there other members who don't have CF but feel comfort here because of the similar symptoms. You are an e-patient and we welcome you.
I know from speaking with Bruce at Ambry that there are 1800 possible mutations. The list seems to be growing. Welcome back and hopefully...
Nervous1...I know there other members who don't have CF but feel comfort here because of the similar symptoms. You are an e-patient and we welcome you.
I know from speaking with Bruce at Ambry that there are 1800 possible mutations. The list seems to be growing. Welcome back and hopefully...
Do your relatives get tested? Dec 17 Poll!
Thanks Emily. This is an informal poll...I tried tweeking the answers...and lost the responses...so some people will have to take it again!...:>j
Do your relatives get tested? Dec 17 Poll!
Thanks Emily. This is an informal poll...I tried tweeking the answers...and lost the responses...so some people will have to take it again!...:>j
Do your relatives get tested? Dec 17 Poll!
Thanks Emily. This is an informal poll...I tried tweeking the answers...and lost the responses...so some people will have to take it again!...:>j
Do your relatives get tested? Dec 17 Poll!
Thanks Emily. This is an informal poll...I tried tweeking the answers...and lost the responses...so some people will have to take it again!...:>j
Do your relatives get tested? Dec 17 Poll!
Thanks Emily. This is an informal poll...I tried tweeking the answers...and lost the responses...so some people will have to take it again!...:>j
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