Guest guest Posted November 18, 2003 Report Share Posted November 18, 2003 Welcome to the most wonderful site for parents of children with cf. Sue Pettit mom to (17 wocf) driving and being the most responsible 17 yo I have ever seen, (13 wocf) playing football, band, and whatever else he can get into, and (11 wcf) into all sports, running full speed doing all she can and still doing great---diagnosed at 8 days of age at LeBonheur Childrens Medical Center in Memphis, Tennessee, now seeing Doctor Lyrene (and other wonderful folks of course) at UAB Children's Hospital Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2003 Report Share Posted November 18, 2003 Welcome Sue to our site. Hope Ethan continues to be well. Tina W., mother of Steph, 18yo wcf hi im new hi im new to this site, my name is sue and i have a 2yr oldwith cf. i live in uk and after reading quite a few of ur posts thought id get intouch. Ethan has been quite well of late and has only been diagnosed for 6 months hope to hear from some of u soon take care love sue _________________________________________________________________ Use MSN Messenger to send music and pics to your friends http://www.msn.co.uk/messenger <http://www.msn.co.uk/messenger> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2003 Report Share Posted November 18, 2003 Hi sue, Welcome! i also have a 2.5 yr old son with cf but was dx right after birth. amy > >Reply-To: cfparents >To: cfparents >Subject: hi im new >Date: Tue, 18 Nov 2003 09:15:32 +0000 > >hi im new to this site, my name is sue and i have a 2yr oldwith cf. i live >in uk and after reading quite a few of ur posts thought id get intouch. >Ethan has been quite well of late and has only been diagnosed for 6 months >hope to hear from some of u soon >take care >love sue > >_________________________________________________________________ >Use MSN Messenger to send music and pics to your friends >http://www.msn.co.uk/messenger > > > > >------------------------------------------- >The opinions and information exchanged on this list should IN NO WAY >be construed as medical advice. > >PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR >TREATMENTS. > >------------------------------------ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2003 Report Share Posted November 18, 2003 hi, thanks for replying, Ethan was only diagnosed because he was seen by a piedatrition who specialised in cf and he only had the test to rule out cf. Imagine the suprise when we found this out. Where abouts are you from? hope to hear from you soon Sue > >Reply-To: cfparents >To: cfparents >Subject: Re: hi im new >Date: Tue, 18 Nov 2003 08:27:49 -0800 > >Hi sue, > >Welcome! i also have a 2.5 yr old son with cf but was dx right after >birth. > >amy > > > > > >Reply-To: cfparents > >To: cfparents > >Subject: hi im new > >Date: Tue, 18 Nov 2003 09:15:32 +0000 > > > >hi im new to this site, my name is sue and i have a 2yr oldwith cf. i >live > >in uk and after reading quite a few of ur posts thought id get intouch. > >Ethan has been quite well of late and has only been diagnosed for 6 >months > >hope to hear from some of u soon > >take care > >love sue > > > >_________________________________________________________________ > >Use MSN Messenger to send music and pics to your friends > >http://www.msn.co.uk/messenger > > > > > > > > > >------------------------------------------- > >The opinions and information exchanged on this list should IN NO WAY > >be construed as medical advice. > > > >PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR > >TREATMENTS. > > > >------------------------------------ > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2003 Report Share Posted November 18, 2003 Welcome Sue. I am glad that you joined us. We learn so much from one another. I am glad that Ethan is doing well. He was 18 months when he got diagnosed. Had he been sick? Gale > hi im new to this site, my name is sue and i have a 2yr oldwith cf. i live > in uk and after reading quite a few of ur posts thought id get intouch. > Ethan has been quite well of late and has only been diagnosed for 6 months > hope to hear from some of u soon > take care > love sue > > _________________________________________________________________ > Use MSN Messenger to send music and pics to your friends > http://www.msn.co.uk/messenger Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 19, 2003 Report Share Posted November 19, 2003 Welcome Sue, This is a great group even when the kids are doing well! My daughter is 5 and has been very well since she was 2. Prior to her 2nd birthday she was sick a lot. Mom of 5 with CF visit our site at http://groups.msn.com/TeamJane > hi im new to this site, my name is sue and i have a 2yr oldwith cf. i live > in uk and after reading quite a few of ur posts thought id get intouch. > Ethan has been quite well of late and has only been diagnosed for 6 months > hope to hear from some of u soon > take care > love sue > > _________________________________________________________________ > Use MSN Messenger to send music and pics to your friends > http://www.msn.co.uk/messenger Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.