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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

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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>

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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.

>

>------------------------------------

>

>

>

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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.

> >

> >------------------------------------

> >

> >

> >

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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

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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

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